<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.0 20040830//EN" "journalpublishing.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="2.0" xml:lang="en" article-type="review-article"><front><journal-meta><journal-id journal-id-type="nlm-ta">Asian Pac Isl Nurs J</journal-id><journal-id journal-id-type="publisher-id">apinj</journal-id><journal-id journal-id-type="index">43</journal-id><journal-title>Asian/Pacific Island Nursing Journal</journal-title><abbrev-journal-title>Asian Pac Isl Nurs J</abbrev-journal-title><issn pub-type="epub">2373-6658</issn><publisher><publisher-name>JMIR Publications</publisher-name><publisher-loc>Toronto, Canada</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">v10i1e75751</article-id><article-id pub-id-type="doi">10.2196/75751</article-id><article-categories><subj-group subj-group-type="heading"><subject>Review</subject></subj-group></article-categories><title-group><article-title>Effectiveness of Interventions to Improve Glycemic Control in US Asian and Pacific Islander Populations With Type 2 Diabetes: Systematic Review and Meta-Analysis</article-title></title-group><contrib-group><contrib contrib-type="author" equal-contrib="yes"><name name-style="western"><surname>Xiao</surname><given-names>Jason</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="fn" rid="equal-contrib1">*</xref></contrib><contrib contrib-type="author" equal-contrib="yes"><name name-style="western"><surname>Yu</surname><given-names>Jielu</given-names></name><degrees>BA</degrees><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="fn" rid="equal-contrib1">*</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Staab</surname><given-names>Erin M</given-names></name><degrees>MPH</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Thomas</surname><given-names>Nikita C</given-names></name><degrees>MSPH</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Wan</surname><given-names>Wen</given-names></name><degrees>PhD</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Deckard</surname><given-names>Amber N</given-names></name><degrees>MPH</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Karter</surname><given-names>Andrew J</given-names></name><degrees>PhD</degrees><xref ref-type="aff" rid="aff3">3</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Peek</surname><given-names>Monica E</given-names></name><degrees>MD, MPH, MS</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Huang</surname><given-names>Elbert S</given-names></name><degrees>MD, MPH</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author" corresp="yes"><name name-style="western"><surname>Laiteerapong</surname><given-names>Neda</given-names></name><degrees>MD, MS</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib></contrib-group><aff id="aff1"><institution>Pritzker School of Medicine, University of Chicago</institution><addr-line>Chicago</addr-line><addr-line>IL</addr-line><country>United States</country></aff><aff id="aff2"><institution>Section of General Internal Medicine, Department of Medicine, University of Chicago</institution><addr-line>5841 S Maryland Ave</addr-line><addr-line>Chicago</addr-line><addr-line>IL</addr-line><country>United States</country></aff><aff id="aff3"><institution>Division of Research, Kaiser Permanente</institution><addr-line>Pleasanton</addr-line><addr-line>CA</addr-line><country>United States</country></aff><contrib-group><contrib contrib-type="editor"><name name-style="western"><surname>Ahn</surname><given-names>Hyochol</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="reviewer"><name name-style="western"><surname>Chiaranai</surname><given-names>Chantira</given-names></name></contrib></contrib-group><author-notes><corresp>Correspondence to Neda Laiteerapong, MD, MS, Section of General Internal Medicine, Department of Medicine, University of Chicago, 5841 S Maryland Ave, Chicago, IL, 60637, United States, 1 773-702-3608; <email>nlaiteer@bsd.uchicago.edu</email></corresp><fn fn-type="equal" id="equal-contrib1"><label>*</label><p>these authors contributed equally</p></fn></author-notes><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>30</day><month>4</month><year>2026</year></pub-date><volume>10</volume><elocation-id>e75751</elocation-id><history><date date-type="received"><day>09</day><month>04</month><year>2025</year></date><date date-type="rev-recd"><day>19</day><month>03</month><year>2026</year></date><date date-type="accepted"><day>03</day><month>04</month><year>2026</year></date></history><copyright-statement>&#x00A9; Jason Xiao, Jielu Yu, Erin M Staab, Nikita C Thomas, Wen Wan, Amber N Deckard, Andrew J Karter, Monica E Peek, Elbert Huang, Neda Laiteerapong. Originally published in the Asian/Pacific Island Nursing Journal (<ext-link ext-link-type="uri" xlink:href="https://apinj.jmir.org">https://apinj.jmir.org</ext-link>), 30.4.2026. </copyright-statement><copyright-year>2026</copyright-year><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Asian/Pacific Island Nursing Journal, is properly cited. The complete bibliographic information, a link to the original publication on <ext-link ext-link-type="uri" xlink:href="https://apinj.jmir.org">https://apinj.jmir.org</ext-link>, as well as this copyright and license information must be included.</p></license><self-uri xlink:type="simple" xlink:href="https://apinj.jmir.org/2026/1/e75751"/><abstract><sec><title>Background</title><p>Asian American and Pacific Islander populations are disproportionately affected by diabetes.</p></sec><sec><title>Objective</title><p>The purpose of this study was to assess the efficacy of nonpharmacologic interventions in reducing hemoglobin A<sub>1c</sub> (HbA<sub>1c</sub>) levels among Asian American or Pacific Islander individuals with type 2 diabetes.</p></sec><sec sec-type="methods"><title>Methods</title><p>A systematic review was conducted using the PubMed, Scopus, PsycInfo, and CINAHL databases, covering studies published from 1985 to 2019. Eligible studies were randomized controlled trials that evaluated nonpharmacologic interventions in outpatient settings for adults with type 2 diabetes in the United States, with at least 50% Asian American or Pacific Islander participants. Data extraction and risk of bias assessment were independently performed by 2 reviewers for each trial. The Cochrane Collaboration risk of bias tool and the Grading of Recommendations, Assessment, Development, and Evaluation approach were used to evaluate quality. Random-effects meta-analyses were conducted to estimate pooled effect sizes.</p></sec><sec sec-type="results"><title>Results</title><p>A total of 1835 articles were screened, with 9 randomized controlled trials meeting the inclusion criteria, comprising 1492 participants, with a median follow-up duration of 6 (IQR 3-12) months. Interventions included diabetes self-management education, bilingual counseling, glucose or weight monitoring, motivational interviewing, and financial support, often tailored to the cultural context of the participants. Pooled analysis of the 9 trials demonstrated a significant average HbA<sub>1c</sub> reduction of &#x2212;0.39% (95% CI &#x2212;0.64% to &#x2212;0.14%; <italic>I</italic>&#x00B2;=65%). Seven studies were judged to have a low risk of bias, 1 study had some concerns, and 1 study was assessed as high risk. The overall strength of evidence was high.</p></sec><sec sec-type="conclusions"><title>Conclusions</title><p>Nonpharmacologic interventions substantively reduced HbA<sub>1c</sub> levels in Asian American or Pacific Islander individuals with type 2 diabetes, particularly when culturally and linguistically tailored.</p></sec></abstract><kwd-group><kwd>type 2 diabetes</kwd><kwd>systematic review</kwd><kwd>meta-analysis</kwd><kwd>Asian American</kwd><kwd>Pacific Islander</kwd><kwd>nonpharmacologic intervention</kwd><kwd>hemoglobin A1c</kwd><kwd>HbA1c</kwd><kwd>glycemic control</kwd></kwd-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><p>Asian American and Pacific Islander (AAPI) persons are disproportionately affected by diabetes, with a higher prevalence of type 2 diabetes compared to White persons, even when individuals have similar BMI or waist circumference [<xref ref-type="bibr" rid="ref1">1</xref>]. The high burden of disease becomes even more apparent when examining disaggregated diabetes prevalence across AAPI ethnic groups [<xref ref-type="bibr" rid="ref1">1</xref>]. For example, in the United States, Filipino men have one of the highest type 2 diabetes rates among all ethnic groups (15.8%), and Korean women are 5 times more likely to be affected by type 2 diabetes compared to non-Hispanic White women [<xref ref-type="bibr" rid="ref2">2</xref>].</p><p>As recommended by the American Diabetes Association, lifestyle and educational interventions are key components of diabetes care and empower patients to make informed health decisions in coping with their disease [<xref ref-type="bibr" rid="ref3">3</xref>]. Such interventions have been shown to be highly effective in promoting diabetes knowledge and self-care behaviors. Diabetes self-management education, for example, has been shown to reduce hemoglobin A<sub>1c</sub> (HbA<sub>1c</sub>) in racial or ethnic minority populations [<xref ref-type="bibr" rid="ref4">4</xref>]. However, only 3 reviews of diabetes interventions have focused on AAPI populations, and they have been limited in terms of geography, heterogeneity, and AAPI subpopulations included [<xref ref-type="bibr" rid="ref5">5</xref>-<xref ref-type="bibr" rid="ref7">7</xref>]. This systematic review and meta-analysis focused on AAPI persons with type 2 diabetes in the United States and aimed to broadly investigate the effect of nonpharmacological interventions on HbA<sub>1c</sub> outcomes.</p></sec><sec id="s2" sec-type="methods"><title>Methods</title><p>This review was registered with the International PROSPERO (CRD42019122625) database and has been reported in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines (Table S1 in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>).</p><sec id="s2-1"><title>Search Strategy</title><p>A systematic search of the PubMed, Scopus, PsycInfo, and CINAHL databases was conducted from 1985 to 2019 without language restrictions, using search terms related to type 2 diabetes, study design, English as a second language, race or ethnicity, and disparities (Table S2 in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>). After duplicate search results were removed, article titles and abstracts were reviewed, and studies that did not meet the criteria were excluded. A full-text review was conducted for the remaining articles. At each stage, articles were reviewed by at least 2 team members. Gray literature was not included in the search.</p></sec><sec id="s2-2"><title>Inclusion and Exclusion Criteria</title><p>We included randomized controlled trials of nonpharmacological interventions intended for adults with type 2 diabetes in the United States and its territories. We excluded inpatient, nursing home, and emergency department&#x2013;based interventions; drugs, devices, surgeries, procedures, and diets; and interventions focused on diabetes prevention, screening, or diagnosis. At least 50% of trial participants had to be Asian, Asian American, Native Hawaiian, or Pacific Islander. Trials had to be at least 3 months in duration and report HbA<sub>1c</sub> as an outcome (Table S3 in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>).</p></sec><sec id="s2-3"><title>Data Extraction</title><p>Data were extracted by 2 independent reviewers using a standardized template, with discrepancies settled by a third reviewer or discussion with the research team. We extracted study characteristics, participant demographics, and HbA<sub>1c</sub> outcomes. We categorized each intervention by its level (eg, individual, interpersonal, or community) and domain (eg, behavioral, sociocultural, or health care system) of influence based on the National Institute on Minority Health and Health Disparities Research Framework [<xref ref-type="bibr" rid="ref8">8</xref>].</p><p>Among the randomized controlled trials (RCTs), HbA<sub>1c</sub> results were reported in any of these 3 ways: (1) a difference in difference between intervention and control groups, (2) a difference between treatment and control groups at a specific follow-up time point, and (3) an HbA<sub>1c</sub> value in a group at a follow-up time point (without group comparison). In the meta-analysis, we used 1 HbA<sub>1c</sub> result per study, prioritizing the type of HbA<sub>1c</sub> using this order.</p></sec><sec id="s2-4"><title>Quality Review</title><p>The Cochrane Collaboration risk of bias tool for RCTs was used to assess the risk of bias for each study [<xref ref-type="bibr" rid="ref9">9</xref>]. Quality of evidence across trials was assessed using the Grading of Recommendations, Assessment, Development, and Evaluation approach. Quality of evidence (ie, degree of confidence that estimated effect approximates true effect) was rated high, moderate, low, or very low based on risk of bias, inconsistency, imprecision, indirectness, and publication bias. A funnel plot and Egger test were used to assess publication bias.</p></sec><sec id="s2-5"><title>Statistical Analysis</title><p>We conducted a random-effects meta-analyses and calculated a weighted average of the estimated effects within individual studies (a pooled effect estimate). We determined weights by the inverse of the within-study variance and between-studies variance for each study. We then constructed a <italic>z</italic> test and its associated 95% CI of pooled intervention effects. Heterogeneity was assessed with the <italic>I</italic><sup>2</sup> statistic. To assess consistency of findings, we used the same methods to perform subgroup analyses based on study populations (ie, Asian, Pacific Islander, and non-English language preferred).</p></sec></sec><sec id="s3" sec-type="results"><title>Results</title><p>Database searches returned 111,289 results. After removing duplicate results and screening titles and abstracts, 1835 articles remained for full-text review. Ultimately, 9 RCTs met all inclusion criteria (<xref ref-type="fig" rid="figure1">Figure 1</xref>) [<xref ref-type="bibr" rid="ref10">10</xref>-<xref ref-type="bibr" rid="ref18">18</xref>]. These enrolled a total of 1492 patients who were primarily aged between 40 and 60 years (<xref ref-type="table" rid="table1">Table 1</xref>); 5 RCTs included all AAPI patients. Specific races or ethnicities included Filipino, Samoan, Hawaiian, Micronesian, Bangladeshi, and Korean. Two RCTs only assessed whether patients identified as Asian or Pacific Islander.</p><fig position="float" id="figure1"><label>Figure 1.</label><caption><p>PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) flow diagram for the systematic review of randomized controlled trials of nonpharmacological interventions among Asian American and Pacific Islander populations with type 2 diabetes (1985&#x2010;2019). HbA<sub>1c</sub>: hemoglobin A<sub>1c</sub>.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="apinj_v10i1e75751_fig01.png"/></fig><table-wrap id="t1" position="float"><label>Table 1.</label><caption><p>Randomized controlled trials of nonpharmacological interventions among Asian American and Pacific Islander populations with type 2 diabetes (1985&#x2010;2019).</p></caption><table id="table1" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Study</td><td align="left" valign="bottom">Location</td><td align="left" valign="bottom">Enrolled/<break/>screened, n/N (%)</td><td align="left" valign="bottom">Arms and participant characteristics</td><td align="left" valign="bottom">Length of follow-up</td></tr></thead><tbody><tr><td align="left" valign="top">Bender et al [<xref ref-type="bibr" rid="ref10">10</xref>], 2017</td><td align="left" valign="top">San Francisco, California</td><td align="char" char="." valign="top">45/113, 39.8%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: culturally adapted mHealth<sup><xref ref-type="table-fn" rid="table1fn1">a</xref></sup> weight loss lifestyle intervention with feedback, coaching, and support (level: individual and interpersonal; domain: behavioral and sociocultural)</p><list list-type="bullet"><list-item><p>Mean age 58 (SD 10) years</p></list-item><list-item><p>60% female</p></list-item><list-item><p>100% Filipino</p></list-item></list></list-item><list-item><p>Control: waitlist</p><list list-type="bullet"><list-item><p>Mean age 57 (SD 10) years</p></list-item><list-item><p>63% female</p></list-item><list-item><p>100% Filipino</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">3 mo</td></tr><tr><td align="left" valign="top">DePue et al [<xref ref-type="bibr" rid="ref11">11</xref>], 2013</td><td align="left" valign="top">American Samoa</td><td align="char" char="." valign="top">268/406, 66%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: culturally adapted education and care coordination delivered by nurse-community health worker team (level: individual and interpersonal; domain: behavioral, sociocultural, and health care system)</p><list list-type="bullet"><list-item><p>Mean age 56 (SD 13) years</p></list-item><list-item><p>57% female</p></list-item><list-item><p>100% Samoan</p></list-item><list-item><p>66% preferred language Samoan</p></list-item></list></list-item><list-item><p>Control: waitlist</p><list list-type="bullet"><list-item><p>Mean age 54 (SD 13) years</p></list-item><list-item><p>65% female</p></list-item><list-item><p>100% Samoan</p></list-item><list-item><p>80% preferred language Samoan</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">12 mo</td></tr><tr><td align="left" valign="top">Fernandes et al [<xref ref-type="bibr" rid="ref12">12</xref>], 2018</td><td align="left" valign="top">Hawaii</td><td align="char" char="." valign="top">320/793, 40.3%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: financial incentives for diabetes management among Medicaid recipients (level: individual; domain: behavioral)</p><list list-type="bullet"><list-item><p>Mean age 49 (SD 11) years</p></list-item><list-item><p>55% female</p></list-item><list-item><p>34% Native Hawaiian or Pacific Islander, 25% multiple races, 20% Asian, 17% White, and 6% Hispanic or Latino</p></list-item></list></list-item><list-item><p>Control: usual care</p><list list-type="bullet"><list-item><p>Mean age 48 (SD 10) years</p></list-item><list-item><p>53% female</p></list-item><list-item><p>33% multiple races, 30% Native Hawaiian or Pacific Islander, 22% Asian, 14% White, and 9% Hispanic or Latino</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">12 mo</td></tr><tr><td align="left" valign="top">Ing et al [<xref ref-type="bibr" rid="ref13">13</xref>], 2016</td><td align="left" valign="top">Oahu, Hawaii</td><td align="char" char="." valign="top">47/65, 72.3%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: bimonthly community facilitator&#x2013; and health professional&#x2013;led support group meetings as follow-up after a culturally tailored, community-based educational intervention (level: individual and interpersonal; domain: behavioral and sociocultural)</p><list list-type="bullet"><list-item><p>Mean age 55 (SD 11) years</p></list-item><list-item><p>40% female</p></list-item><list-item><p>56% Native Hawaiian, 32% Micronesian, and 8% Filipino</p></list-item></list></list-item><list-item><p>Control: bimonthly postcards reminders about diabetes self-management as follow-up</p><list list-type="bullet"><list-item><p>Mean age 54 (SD 9) years</p></list-item><list-item><p>62% female</p></list-item><list-item><p>59% Native Hawaiian and 36% Micronesian</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">3 mo</td></tr><tr><td align="left" valign="top">Islam et al [<xref ref-type="bibr" rid="ref14">14</xref>], 2018</td><td align="left" valign="top">New York, New York</td><td align="char" char="." valign="top">336/880, 38.1%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: culturally adapted, community health worker&#x2013;led educational intervention including 5 group sessions and 2 one-on-one sessions (level: individual; domain: behavioral and sociocultural)</p><list list-type="bullet"><list-item><p>Mean age 54 (SD 11) years</p></list-item><list-item><p>40% female</p></list-item><list-item><p>100% Bangladeshi</p></list-item><list-item><p>55% limited English proficiency</p></list-item></list></list-item><list-item><p>Control: one culturally adapted community health worker&#x2013;led educational session</p><list list-type="bullet"><list-item><p>Mean age 56 (SD 10) years</p></list-item><list-item><p>40% female</p></list-item><list-item><p>100% Bangladeshi</p></list-item><list-item><p>59% limited English proficiency</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">6 mo</td></tr><tr><td align="left" valign="top">Kim et al [<xref ref-type="bibr" rid="ref15">15</xref>], 2009</td><td align="left" valign="top">Baltimore and Washington DC area</td><td align="char" char="." valign="top">83/224, 37%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: culturally tailored education, home glucose monitoring with tele-transmission, and nurse telephone counseling (level: individual; domain: behavioral and sociocultural)</p><list list-type="bullet"><list-item><p>Mean age 57 (SD 8) years</p></list-item><list-item><p>51% female</p></list-item><list-item><p>100% Korean</p></list-item><list-item><p>Predominantly Korean speaking</p></list-item></list></list-item><list-item><p>Control: waitlist</p><list list-type="bullet"><list-item><p>Mean age 56 (SD 8) years</p></list-item><list-item><p>38% female</p></list-item><list-item><p>100% Korean</p></list-item><list-item><p>Predominantly Korean speaking</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">6 mo</td></tr><tr><td align="left" valign="top">Kim et al [<xref ref-type="bibr" rid="ref16">16</xref>], 2015</td><td align="left" valign="top">Baltimore and Washington DC area</td><td align="char" char="." valign="top">250/597, 41.8%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: community-based, culturally tailored, multimodal behavioral intervention including group education sessions and coaching by nurses and community health workers (level: individual; domain: behavioral and sociocultural)</p><list list-type="bullet"><list-item><p>Mean age 59 (SD 8) years</p></list-item><list-item><p>41% female</p></list-item><list-item><p>100% Korean</p></list-item><list-item><p>61% see a Korean-speaking doctor</p></list-item></list></list-item><list-item><p>Control: waitlist</p><list list-type="bullet"><list-item><p>Mean age 58 (SD 9) years</p></list-item><list-item><p>45% female</p></list-item><list-item><p>100% Korean</p></list-item><list-item><p>59% see a Korean-speaking doctor</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">12 mo</td></tr><tr><td align="left" valign="top">Ratanawongsa et al [<xref ref-type="bibr" rid="ref17">17</xref>], 2014</td><td align="left" valign="top">San Francisco, California</td><td align="char" char="." valign="top">362/910, 39.7%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: culturally tailored, automated telephone self-management support and health coaching intervention (level: individual and interpersonal; domain: behavioral, sociocultural, and health care system)</p><list list-type="bullet"><list-item><p>Mean age 57 (SD 8) years</p></list-item><list-item><p>77% female</p></list-item><list-item><p>61% Asian or Pacific Islander, 25% Latino, 6% Black, and 6% White</p></list-item><list-item><p>54% Cantonese speaking and 20% Spanish speaking</p></list-item></list></list-item><list-item><p>Control: waitlist</p><list list-type="bullet"><list-item><p>Mean age 55 (SD 9) years</p></list-item><list-item><p>71% female</p></list-item><list-item><p>62% Asian or Pacific Islander, 20% Latino, 10% Black, and 7% White</p></list-item><list-item><p>55% Cantonese speaking and 18% Spanish speaking</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">6 mo</td></tr><tr><td align="left" valign="top">Sinclair et al [<xref ref-type="bibr" rid="ref18">18</xref>], 2013</td><td align="left" valign="top">Hawaii</td><td align="char" char="." valign="top">82/91, 90.1%</td><td align="left" valign="top"><list list-type="bullet"><list-item><p>Intervention: culturally adapted, community-based educational intervention (level: individual and interpersonal; domain: behavioral and sociocultural)</p><list list-type="bullet"><list-item><p>Mean age 53 (SD 12) years</p></list-item><list-item><p>63% female</p></list-item><list-item><p>100% Native Hawaiian, Pacific Islander, or Filipino</p></list-item></list></list-item><list-item><p>Control: waitlist</p><list list-type="bullet"><list-item><p>Mean age 55 (SD 10) years</p></list-item><list-item><p>62% female</p></list-item><list-item><p>100% Native Hawaiian, Pacific Islander, or Filipino</p></list-item></list></list-item></list></td><td align="char" char="." valign="top">3 mo</td></tr></tbody></table><table-wrap-foot><fn id="table1fn1"><p><sup>a</sup>mHealth: mobile health.</p></fn></table-wrap-foot></table-wrap><p>Most RCTs (n=7) included a component of diabetes self-management education (DSME) in the intervention arm. Other strategies consisted of bilingual counseling (n=4), glucose or weight self-monitoring (n=3), motivational interviewing (n=1), and financial support (n=1). Approximately all (n=8) studies modified some element of their intervention toward the specific cultures of their study populations. Per the National Institute on Minority Health and Health Disparities Research Framework, studies were conducted at the individual (n=9) and interpersonal levels of influence (n=5), targeting primarily behavioral (n=9) and sociocultural domains (n=8). For controls, 6 RCTs used waitlist patients, 2 used a minimal intensity intervention, and 1 used usual care.</p><p>Overall, individuals were followed for a median of 6 (range 3&#x2010;12) months. The interventions on average resulted in a &#x2212;0.39% (95% CI &#x2212;0.64 to &#x2212;0.14%; <italic>I</italic><sup>2</sup>=65%; <xref ref-type="fig" rid="figure2">Figure 2</xref>; <xref ref-type="table" rid="table2">Table 2</xref>) decrease in HbA<sub>1c</sub>. A similar pattern was observed with subgroup analyses for Asian individuals (n=5), with an average reduction in HbA<sub>1c</sub> by &#x2212;0.43% (95% CI &#x2212;0.66 to &#x2212;0.20%; <italic>I</italic><sup>2</sup>=43%) and for Pacific Islander individuals (n=3), with a decrease of &#x2212;0.62 % (95% CI &#x2212;0.94 to &#x2212;0.29%; <italic>I</italic><sup>2</sup>=0%). For individuals who preferred non-English language (n=5), these interventions on average decreased HbA<sub>1c</sub> levels by &#x2212;0.47% (95% CI &#x2212;0.70% to &#x2212;0.23%; <italic>I</italic><sup>2</sup>=45%). The most effective interventions specifically described using culturally tailored and/or language-tailored modalities of DSME.</p><table-wrap id="t2" position="float"><label>Table 2.</label><caption><p>Meta-analysis of effects of nonpharmacological interventions on hemoglobin A<sub>1c</sub> (HbA<sub>1c</sub>) outcomes among Asian American and Pacific Islander populations with type 2 diabetes (1985&#x2010;2019).</p></caption><table id="table2" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom"/><td align="left" valign="bottom">Trials, n (%)</td><td align="left" valign="bottom">HbA<sub>1c</sub><sup><xref ref-type="table-fn" rid="table2fn1">a</xref></sup>, weighted mean difference (95% Cl)</td><td align="left" valign="bottom"><italic>I</italic><sup>2</sup> statistic (%)</td></tr></thead><tbody><tr><td align="left" valign="top" colspan="4">Overall</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Asian or Pacific Islander</td><td align="left" valign="top">9 (100)</td><td align="left" valign="top">&#x2212;0.39 (&#x2212;0.64 to &#x2212;0.14)</td><td align="left" valign="top">65</td></tr><tr><td align="left" valign="top" colspan="4">Subgroup</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Asian</td><td align="left" valign="top">5 (56)</td><td align="left" valign="top">&#x2212;0.43 (&#x2212;0.66 to &#x2212;0.20)</td><td align="left" valign="top">43</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Pacific Islander</td><td align="left" valign="top">3 (34)</td><td align="left" valign="top">&#x2212;0.62 (&#x2212;0.94 to &#x2212;0.29)</td><td align="left" valign="top">0</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Non-English language preferred</td><td align="left" valign="top">5 (56)</td><td align="left" valign="top">&#x2212;0.47 (&#x2212;0.70 to &#x2212;0.23)</td><td align="left" valign="top">45</td></tr></tbody></table><table-wrap-foot><fn id="table2fn1"><p><sup>a</sup>HbA<sub>1c</sub>: hemoglobin A<sub>1c</sub>.</p></fn></table-wrap-foot></table-wrap><fig position="float" id="figure2"><label>Figure 2.</label><caption><p>Forest plot of hemoglobin A<sub>1c</sub> outcomes in nonpharmacological intervention trials among Asian American and Pacific Islander populations with type 2 diabetes (1985&#x2010;2019) [<xref ref-type="bibr" rid="ref10">10</xref>-<xref ref-type="bibr" rid="ref18">18</xref>].</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="apinj_v10i1e75751_fig02.png"/></fig><p>Using the Cochrane Collaboration risk of bias for randomized trials tool, 7 of the 9 studies were determined to be at low risk of bias (Table S4 in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>). One study [<xref ref-type="bibr" rid="ref12">12</xref>] had some concerns in the domain of deviations from the intended intervention, and another study [<xref ref-type="bibr" rid="ref17">17</xref>] was at high risk for bias in the domain of missing outcome data. Publication bias was evaluated visually by plotting changes in HbA<sub>1c</sub> by study on a funnel plot, where the y-axis represents study size and the x-axis the size of effect found (Figure S1 in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>). Of the 9 RCTs, 8 fell within the expected 95%, and approximate symmetry was achieved with the exception of the single study, whose intervention relied solely on financially incentivizing diabetes self-management. Additionally, 1 study with a small sample size (n=47) and relatively large HbA<sub>1c</sub> SD at baseline affected the vertical distribution. The Egger test indicated no evidence of publication bias (<italic>P</italic>=.22). Quality of evidence was high by the GRADE (Grading of Recommendations, Assessment, Development, and Evaluation) approach (Table S5 in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>).</p></sec><sec id="s4" sec-type="discussion"><title>Discussion</title><p>We investigated the efficacy of nonpharmacologic interventions for type 2 diabetes in lowering HbA<sub>1c</sub> in Asian American and Pacific Islander individuals. Our systematic review and meta-analysis identified a substantive reduction of HbA<sub>1c</sub>, with an average change of &#x2212;0.39% over 6 months. Most interventions incorporated components of DSME and social engagement such as counseling or other interpersonal interactions. Furthermore, nearly all of the interventions tailored their approach based on the languages and cultures of their target population, often collaborating with community health workers or community-based organizations.</p><p>Identifying evidence-based ways to enhance diabetes management is essential for populations at greater risk for type 2 diabetes development and progression, including AAPI persons. AAPI populations have experienced alarming rises in diabetes; for instance, one study found a 68% increase in incidence between 1993 and 2001, the highest among all racial or ethnic groups [<xref ref-type="bibr" rid="ref19">19</xref>]. Consequently, the American Diabetes Association has incorporated race or ethnicity into adult screening guidelines, and people with AAPI race or ethnicity are considered a &#x201C;high-risk&#x201D; population [<xref ref-type="bibr" rid="ref20">20</xref>]. Furthermore, while AAPI race or ethnicity is comprised of many heterogeneous populations, current practices typically aggregate them as &#x201C;Asian&#x201D; or &#x201C;Other,&#x201D; when in reality over 40 ethnic subgroups fall under this categorization [<xref ref-type="bibr" rid="ref21">21</xref>]. Encouragingly, in this review, few studies reported AAPI as a single group, and a broad range of AAPI subpopulations were represented (Filipino, Samoan, Hawaiian, Micronesian, Bangladeshi, and Korean). Heterogeneity was moderately high for overall results but lower in subgroup analyses. Data aggregation across AAPI subpopulations can mask higher-risk subpopulations and negatively impact screening, diagnosis, and treatment. For example, the DISTANCE study, which delineated AAPI subgroups when estimating diabetes rates, found that Pacific Islander, South Asian, and Filipino individuals had the highest prevalence of diabetes (18.3%, 15.9%, and 16.1%, respectively) across all racial or ethnic categories [<xref ref-type="bibr" rid="ref22">22</xref>]. They also detected substantial differences in the rates of diabetes-related complications across AAPI subgroups [<xref ref-type="bibr" rid="ref22">22</xref>].</p><p>AAPI persons constitute 7.7% of the US population and are one of the fastest growing racial or ethnic groups. Nonetheless, research funding for studies focusing on AAPI populations has not progressed over the past several decades. From 1986 to 2000, AAPI was represented in 0.2% of health-related grants across 7 federal agencies [<xref ref-type="bibr" rid="ref23">23</xref>]. Between 1992 and 2018, 0.2% of the National Institutes of Health budget was allocated to 529 AAPI-related clinical research projects [<xref ref-type="bibr" rid="ref24">24</xref>]. In the same time frame, inclusion of Native Hawaiians and Pacific Islanders in extramural National Institutes of Health&#x2013;defined phase 3 clinical trials decreased from 0.3% (n=1011) to 0.2% (n=271) [<xref ref-type="bibr" rid="ref24">24</xref>]. Given the small and shrinking number of RCTs among people with AAPI race or ethnicity, additional RCTs are needed to further our understanding of optimal strategies to manage type 2 diabetes in people with AAPI race or ethnicity.</p><p>Nonpharmacological interventions can meaningfully improve prevention and management of diabetes and have been found to be cost-effective; however, underrepresentation of AAPI persons in trials reduces generalizability [<xref ref-type="bibr" rid="ref25">25</xref>-<xref ref-type="bibr" rid="ref28">28</xref>]. For instance, the landmark Look Action for Health in Diabetes trial showed that intensive lifestyle interventions improved glycemic control and cardiovascular outcomes [<xref ref-type="bibr" rid="ref29">29</xref>]. Although the Look Action for Health in Diabetes trial aimed to recruit at least a third of participants from racial and ethnic minority groups, there were only 50 (&#x003C;2%) AAPI participants [<xref ref-type="bibr" rid="ref30">30</xref>]. A meta-analysis of 16 randomized lifestyle intervention trials in general populations with type 2 diabetes found an average change of &#x2212;0.37% in HbA<sub>1c</sub> [<xref ref-type="bibr" rid="ref31">31</xref>]. While this meta-analysis did not report stratified results or primarily enroll AAPI populations, their reduction in HbA<sub>1c</sub> is very similar to our findings (&#x2212;0.39%), providing some reassurance in the generalizability of larger studies.</p><p>Given the tremendous diversity of genetics, culture, diet, and lifestyle within the AAPI category, the effectiveness of specific interventions may vary by population. With our limited sample size, we were unable to directly compare types of interventions. However, we identified DSME as the most common shared component in these studies, which is one form of intervention that is strongly supported in the literature. In a systematic review of 118 randomized trials for adults with type 2 diabetes, DSME resulted in a &#x2212;0.74% reduction in HbA<sub>1c</sub> [<xref ref-type="bibr" rid="ref32">32</xref>]. Furthermore, the study found that combining individual and group engagement resulted in greater reduction in HbA<sub>1c</sub>. However, studies that aggregate data at this level are unable to delineate racial or ethnic differences. Recently, different meta-analyses have demonstrated that nonpharmacologic interventions such as DSME may differ in effectiveness based on the population in focus. For example, in 2 meta-analyses, DSME interventions were shown to reduce HbA<sub>1c</sub> (&#x2212;0.24% and &#x2212;0.25%) in Latino individuals with type 2 diabetes [<xref ref-type="bibr" rid="ref33">33</xref>,<xref ref-type="bibr" rid="ref34">34</xref>]. However, in another meta-analysis, DSME did not reduce HbA<sub>1c</sub> in African American persons [<xref ref-type="bibr" rid="ref35">35</xref>]. Mixed results have been reported in other meta-analyses, in which lifestyle interventions were effective in lowering HbA<sub>1c</sub> for White individuals but not Black or African individuals or Hispanic populations [<xref ref-type="bibr" rid="ref36">36</xref>]. Another systematic review found that lifestyle intervention reduced the incidence of type 2 diabetes more in the &#x201C;(predominantly) White&#x201D; group compared to the Asian group [<xref ref-type="bibr" rid="ref37">37</xref>]. Moreover, beyond HbA<sub>1c</sub>, significant differences may exist in the impact on 2-hour glucose, BMI, and waist circumference depending on the racial or ethnic subgroup [<xref ref-type="bibr" rid="ref38">38</xref>]. Taken together, these studies suggest that a uniform approach for nonpharmacologic management of type 2 diabetes would not lead to optimal health outcomes or reduction in health disparities.</p><p>In a report by the National Heart, Blood, and Lung Institute on improving cardiometabolic risk factors in Asian American individuals, the committee recommended more research to understand the social and cultural contexts of lifestyle interventions, perceptions, and barriers to addressing such risk factors [<xref ref-type="bibr" rid="ref39">39</xref>]. This notion has taken root in the United States&#x2014;for example, several studies focusing on South Asian individuals, such as the South Asian Healthy Lifestyle Intervention, use culturally tailored strategies to reduce cardiovascular risk factors [<xref ref-type="bibr" rid="ref40">40</xref>]. Reviewing lifestyle interventions in South Asian individuals found that tailoring interventions to linguistic and cultural norms such as modifying traditional Indian cooking and incorporating physical activities from South Asia were effective in lowering HbA<sub>1c</sub> [<xref ref-type="bibr" rid="ref41">41</xref>].</p><p>In our study, 8 [<xref ref-type="bibr" rid="ref10">10</xref>,<xref ref-type="bibr" rid="ref11">11</xref>,<xref ref-type="bibr" rid="ref13">13</xref>-<xref ref-type="bibr" rid="ref18">18</xref>] of the 9 studies culturally tailored their intervention prior to implementation&#x2014;for instance, Ing et al [<xref ref-type="bibr" rid="ref13">13</xref>] in Hawaii created their intervention by partnering with local organizations and based their educational content on prior focus groups created in the community, highlighting relevant images, foods, and physical activities in Hawaii. In other studies, community health workers, who often are trusted members of the community, were employed to effectively carry out interventions in the study population. Overall, these studies highlight the potential benefits of actively partnering within and beyond traditional public health institutions, including community organizations and services, to bring culturally and linguistically appropriate care. Given the financial and logistical barriers to providing these more customized interventions to patients, telemedicine may be a promising approach. In the studies we reviewed, telephone counseling and remote blood glucose monitoring were strategies that proved effective in reducing HbA<sub>1c</sub>. Results of recent meta-analyses also support the effectiveness and potential cost-saving of telehealth and digital interventions for improving glycemic control [<xref ref-type="bibr" rid="ref42">42</xref>-<xref ref-type="bibr" rid="ref47">47</xref>]. Therefore, culturally adapting interventions, collaborating with community organizations, and using telemedicine and digital health tools are all possible strategies that health care systems can incorporate to improve healthy behaviors and outcomes for type 2 diabetes in AAPI communities.</p><p>This study has several limitations. First, a relatively small number of trials met all inclusion criteria for this meta-analysis. In part, this reflects a greater need for clinical trials to increase enrollment across underrepresented races or ethnicities, including those of AAPI backgrounds. While not feasible to conduct comparable studies by individual subgroup, stratifying AAPI populations by a limited number of diabetes and cardiovascular risk groups may prove useful to guide screening and management. Additionally, as with any meta-analysis, the dissimilarity of interventions makes differences in effect on HbA<sub>1c</sub> difficult to compare. This is particularly true with nonpharmacologic interventions, given that each study developed a unique intervention for their populations. A larger sample size and further exploration of heterogeneity related to intervention approaches and study populations would be useful for understanding the generalizability of findings. Finally, it is possible that there are intervention studies published in the gray literature or indexed in other databases that were not included in this analysis.</p><p>In summary, this meta-analysis examined 9 nonpharmacologic interventions for type 2 diabetes for primarily AAPI populations. Random-effects meta-analysis found that such interventions substantively lowered HbA<sub>1c</sub>, offering support to leverage these interventions in clinical practice and community efforts. Successful interventions were culturally tailored and often used diabetes self-management education. More RCTs are needed to add to the small body of literature of effective nonpharmacologic interventions for AAPI populations with type 2 diabetes. Additionally, future studies are required to evaluate how other markers of cardiovascular risk and systemic health can be improved in these populations. Developing evidence-based approaches to managing type 2 diabetes in AAPI populations will further reduce the burden of diabetes in the United States and enhance quality of care.</p></sec></body><back><ack><p>Portions of this work were presented at the American Diabetes Association Scientific Sessions in June 2022.</p></ack><notes><sec><title>Funding</title><p>Primary funding for this research was received from the National Institute on Minority Health and Health Disparities (R01MD013420). Additional support was received from the National Institute of Diabetes and Digestive and Kidney Diseases (2P30DK092949 and P30DK092924).</p></sec><sec><title>Data Availability</title><p>Data collection forms and datasets generated and analyzed in this study are available from the corresponding author upon reasonable request.</p></sec></notes><fn-group><fn fn-type="con"><p>JX and JY acquired and interpreted the data and drafted the work. EMS and NL made substantial contributions to the design, acquired and interpreted the data, and reviewed the work for critical important intellectual content. AND acquired and interpreted the data and reviewed the work for critical intellectual content. AJK, MEP, and ESH made substantial contributions to the design and reviewed the work for critical important intellectual content. NCT and WW analyzed the data and reviewed it critically for important intellectual content. All authors provided final approval before publishing and agree to be accountable for the accuracy of the work. NL is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.</p></fn><fn fn-type="conflict"><p>None declared.</p></fn></fn-group><glossary><title>Abbreviations</title><def-list><def-item><term id="abb1">AAPI</term><def><p>Asian American and Pacific Islander</p></def></def-item><def-item><term id="abb2">DSME</term><def><p>diabetes self-management education</p></def></def-item><def-item><term id="abb3">GRADE</term><def><p>Grading of Recommendations, Assessment, Development, and Evaluation</p></def></def-item><def-item><term id="abb4">HbA<sub>1c</sub></term><def><p>hemoglobin A<sub>1c</sub></p></def></def-item><def-item><term id="abb5">PRISMA</term><def><p>Preferred Reporting Items for Systematic Reviews and Meta-Analyses</p></def></def-item><def-item><term id="abb6">RCT</term><def><p>randomized controlled 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