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Effectiveness of a Diabetes Self-Management Program Among Ethnic Minority Elderly in Rural Thailand (DSM-EME)

2026年6月21日 更新者:Taipei Medical University

The Effectiveness of Diabetes Self-Management Intervention on Glycemic Control, Self-management and Psychological Distress for Ethnic Minority Elderly in Rural Areas in Thailand: A Randomized Controlled Trial

Type 2 diabetes is a serious health condition that affects many older adults from ethnic minority communities in Northern Thailand. These populations, often referred to as hill tribes, include groups such as Akha, Lahu, Hmong, and Lisu who live in remote mountainous areas of Chiang Rai Province. Previous research has found that the prevalence of type 2 diabetes among ethnic minority elderly in Thailand is 16.8%, which is higher than the general Thai population. Many of these individuals have difficulty managing their diabetes because of low literacy, limited access to healthcare, language barriers, and poverty.

The purpose of this study was to test whether a structured Diabetes Self-Management (DSM) program could help ethnic minority older adults (aged 60 years or older) improve their blood sugar control, increase their ability to manage diabetes on their own, and reduce emotional distress related to diabetes.

This study used a cluster randomized controlled trial design. Villages in Chiang Rai Province were randomly assigned to either the DSM intervention group or the usual care group. A total of 108 participants (54 per group) were enrolled. Participants in the intervention group attended a 6-week education program with weekly interactive sessions covering diabetes knowledge, healthy eating, physical activity, medication management, problem solving, risk reduction, and emotional coping. Two home visits were also provided at Weeks 8 and 10. Participants in the usual care group received standard brief discharge education and routine follow-up visits.

The main outcome measured was the change in HbA1c (a blood test that shows average blood sugar levels over the past 2 to 3 months) from the start of the study to 12 weeks later. Additional outcomes included changes in diabetes self-management behaviors and diabetes-related psychological distress, measured using validated questionnaires.

調査の概要

詳細な説明

This study employed a cluster randomized controlled trial (cRCT) design to evaluate the effectiveness of a culturally tailored Diabetes Self-Management (DSM) intervention among ethnic minority elderly (EME) aged 60 years or older with type 2 diabetes mellitus (T2DM) in rural Chiang Rai Province, Northern Thailand.

BACKGROUND AND RATIONALE:

Ethnic minority populations in Northern Thailand, commonly referred to as hill tribes, experience disproportionately high rates of T2DM compared to the general Thai population. These communities face multiple barriers to effective diabetes management, including geographic isolation, low health literacy, limited Thai language proficiency, cultural differences in health beliefs, and restricted access to healthcare services. Despite the well-established evidence supporting diabetes self-management education for improving glycemic outcomes, few interventions have been designed specifically for low-literacy, culturally diverse elderly populations in low-resource rural settings.

THEORETICAL FRAMEWORK:

The DSM intervention was developed based on the Chronic Care Model (CCM), which emphasizes patient-centered care through self-management support, community resource linkage, health system integration, clinical information systems, and decision support. The intervention content was informed by the seven core self-management skills defined by the American Association of Diabetes Educators (AADE7): healthy eating, being active, monitoring, taking medications, problem solving, reducing risks, and healthy coping.

RANDOMIZATION AND ALLOCATION:

Eighteen villages with ethnic minority populations were identified and stratified into two groups of nine villages each based on geographical region, proportion of ethnic minority residents, and expected T2DM caseloads. Villages were randomly allocated in a 1:1 ratio to either the DSM intervention arm or the usual care control arm. The randomization sequence was generated by an independent statistician using a computer-based random number generator. Allocation concealment was maintained through sealed opaque envelopes opened only after each village confirmed participation. Recruitment within villages was completed prior to revealing allocation to recruiters to minimize recruitment bias.

INTERVENTION ARM:

Participants in the intervention arm received a 6-week structured DSM program consisting of one interactive session per week, each lasting 1 to 3 hours. Sessions were delivered by a multidisciplinary team including endocrinologists, nurse practitioners, dieticians, and village health volunteers (VHVs). Teaching methods were specifically adapted for low-literacy populations and incorporated visual flipcharts, picture-based symptom diaries with color codes and symbols, hands-on food demonstrations using locally available ingredients, glucometer training, role-play scenarios, and group discussions conducted with native-language translation support from VHVs.

Week 1 focused on diabetes fundamentals and symptom management, including recognition of hypoglycemia, hyperglycemia, and emotional distress. Week 2 addressed culturally appropriate healthy eating using the plate model and hand method for portion control. Week 3 introduced safe physical activities adapted for elderly bodies, including walking, stretching, and light gardening. Week 4 covered medication adherence and blood glucose self-monitoring with hands-on glucometer practice. Week 5 addressed problem solving and risk reduction through case-scenario role-plays for hypoglycemia management and daily foot care. Week 6 focused on healthy coping strategies, stress management, and effective use of local healthcare services.

Following the 6-week workshop phase, two home visits were conducted at Weeks 8 and 10 by nurses and VHVs to reinforce skills, review symptom and diet records, check medication adherence, and provide emotional support.

CONTROL ARM:

Participants in the control arm received standard usual care consisting of a one-time 10 to 15 minute face-to-face discharge education session delivered by a nurse practitioner not involved in the study intervention. Content included general information about T2DM, dietary advice, exercise recommendations, risk factor awareness, and self-monitoring instructions. No teach-back method, interactive activities, or structured follow-up education was provided. Participants attended scheduled outpatient follow-up visits as per the routine hospital system.

CONTAMINATION PREVENTION:

Separate teams delivered the intervention and control activities, and sessions were scheduled independently across clusters to minimize the risk of contamination between groups.

BLINDING:

Participants and intervention providers could not be blinded due to the nature of the behavioral intervention. Outcome assessors who collected HbA1c measurements and administered questionnaires were blinded to group allocation and were not involved in intervention delivery.

OUTCOME ASSESSMENT:

All outcomes were assessed at baseline (Week 0) and at 12 weeks after the start of the intervention. The primary outcome was change in glycated hemoglobin (HbA1c), measured via blood test at sub-district health promoting hospitals. Secondary outcomes included change in diabetes self-management behaviors measured by the Diabetes Self-Management Questionnaire (DSMQ, Thai version, 30 items across five domains, scored 30 to 150), and change in diabetes-related psychological distress measured by the 17-item Diabetes Distress Scale (DDS-17, four dimensions, 6-point Likert scale).

SAMPLE SIZE:

The sample size was calculated based on an effect size of 0.77 from a previous related study, with a significance level of 0.05 and statistical power of 0.90, yielding 45 participants per group. After accounting for an anticipated 20% attrition rate, 54 participants per group (108 total) were required.

STATISTICAL ANALYSIS:

Baseline demographic characteristics were described using means and standard deviations for continuous variables and frequencies and percentages for categorical variables. Paired t-tests and independent t-tests were used to compare within-group and between-group differences in study outcomes.

ETHICAL CONSIDERATIONS:

The study was approved by the Chiang Rai Province Public Health Research Ethics Committee (Approval No. CRPPHO 059/2568) and the Taipei Medical University-Joint Institutional Review Board (Approval No. N202511006). All procedures adhered to the principles of the Declaration of Helsinki. Gatekeeper consent was obtained from village leaders and local health staff prior to enrollment. Written informed consent or a thumbprint with a witness signature was obtained from each participant.

研究の種類

介入

入学 (実際)

108

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Changwat Chiang Rai
      • Chiang Rai、Changwat Chiang Rai、タイ、57100
        • Sub-district Health Promoting Hospitals (SDHPHs), Chiang Rai Province

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Ethnic minority elderly aged 60 years or older residing in rural mountainous villages in Chiang Rai Province, Northern Thailand (including Akha, Lahu, Hmong, and Lisu communities)
  • Diagnosed with type 2 diabetes mellitus (T2DM) for at least one year
  • HbA1c level greater than 6.5%
  • Mini-Mental State Examination (MMSE) score of 24 or higher
  • Ability to communicate in Thai language
  • Willing and able to provide written informed consent or thumbprint with witness signature

Exclusion Criteria:

  • Unable to complete the informed consent process
  • Mini-Mental State Examination (MMSE) score below 24, indicating possible cognitive impairment
  • Severe or unstable medical conditions that would preclude participation in a 6-week group education program (e.g., acute hospitalization, severe mobility limitations requiring full-time assistance)
  • Currently participating in another diabetes education or self-management intervention study

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:支持療法
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:Diabetes Self-Management Intervention Group
Participants in villages allocated to the intervention arm received a 6-week structured Diabetes Self-Management Education (DSME) program consisting of weekly interactive sessions (1 to 3 hours each) delivered by a multidisciplinary team including endocrinologists, nurse practitioners, dieticians, and village health volunteers. Content covered seven core self-management skills: symptom management, healthy eating, physical activity, medication adherence and glucose monitoring, problem solving, risk reduction, and healthy coping. Teaching methods were adapted for low-literacy populations using visual flipcharts, picture-based diaries, food demonstrations, hands-on glucometer training, role-play scenarios, and native-language translation support. Two follow-up home visits were conducted at Weeks 8 and 10 for skills reinforcement and emotional support.
A culturally tailored 6-week diabetes self-management education program grounded in the Chronic Care Model and the seven core self-management skills defined by the American Association of Diabetes Educators. The program consisted of six weekly interactive group sessions: Week 1 covered diabetes fundamentals and symptom management; Week 2 addressed culturally appropriate healthy eating using the plate model and hand method for portion control; Week 3 introduced safe physical activities adapted for elderly participants; Week 4 focused on medication adherence and blood glucose self-monitoring with hands-on glucometer practice; Week 5 addressed problem solving and risk reduction through role-play scenarios for hypoglycemia management and daily foot care; Week 6 covered healthy coping strategies, stress management, and effective use of local healthcare services. Sessions were delivered by endocrinologists, nurse practitioners, dieticians, and village health volunteers who provided native-la
アクティブコンパレータ:Usual Care Control Group
Participants in villages allocated to the control arm received standard usual care provided by local health services. This consisted of a one-time 10 to 15 minute face-to-face discharge education session delivered by a nurse practitioner not involved in the study intervention. Content included general information about type 2 diabetes, dietary advice, exercise recommendations, risk factor awareness, and self-monitoring instructions. No teach-back method, interactive activities, structured follow-up education, or home visits were provided. Participants attended scheduled outpatient follow-up visits as per the routine hospital system.
Standard guideline-based discharge education for type 2 diabetes consisting of a one-time 10 to 15 minute face-to-face verbal education session delivered by a nurse practitioner not involved in the study intervention. Content included basic knowledge of type 2 diabetes, general dietary advice, exercise recommendations, risk factor awareness, complication prevention guidance, and self-monitoring instructions. A hospital-provided leaflet was given if available. No interactive activities, teach-back method, structured follow-up education, or home visits were included. Participants attended routine outpatient follow-up visits as scheduled by the hospital system.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Glycated Hemoglobin (HbA1c)
時間枠:Baseline (Week 0) and 12 weeks after the start of the intervention
Change in HbA1c level (%) from baseline to 12 weeks. HbA1c was measured via venous blood sample collected at sub-district health promoting hospitals (SDHPHs) by nurse practitioners. HbA1c reflects average blood glucose control over the preceding 2 to 3 months. A decrease in HbA1c indicates improved glycemic control.
Baseline (Week 0) and 12 weeks after the start of the intervention

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in Diabetes Self-Management Behaviors (DSMQ)
時間枠:Baseline (Week 0) and 12 weeks after the start of the intervention
Change in total score on the Diabetes Self-Management Questionnaire (DSMQ), Thai version, from baseline to 12 weeks. The DSMQ consists of 30 items across five domains: general health, diet, exercise, medication, and eye care. Each item is rated on a 5-point scale (1=never do to 5=always). Total scores range from 30 to 150. Higher scores indicate better self-management behaviors.
Baseline (Week 0) and 12 weeks after the start of the intervention
Change in Diabetes-Related Psychological Distress (DDS-17)
時間枠:Baseline (Week 0) and 12 weeks after the start of the intervention
Change in mean score on the 17-item Diabetes Distress Scale (DDS-17) from baseline to 12 weeks. The DDS-17 measures distress across four dimensions: emotional burden (5 items), physician-related distress (4 items), regimen-related distress (5 items), and interpersonal distress (3 items). Items are rated on a 6-point Likert scale (1=no problem to 6=serious problem). Higher scores indicate greater psychological distress.
Baseline (Week 0) and 12 weeks after the start of the intervention

協力者と研究者

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出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年11月20日

一次修了 (実際)

2026年2月19日

研究の完了 (実際)

2026年2月19日

試験登録日

最初に提出

2026年6月21日

QC基準を満たした最初の提出物

2026年6月21日

最初の投稿 (実際)

2026年6月25日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月25日

QC基準を満たした最後の更新が送信されました

2026年6月21日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • TMU-JIRB: N202511006
  • CRPPHO 059/2568 (その他の識別子:Chiang Rai Province Public Health Research Ethics Committee (CRPPHO))

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

The datasets generated during the current study are not publicly available due to the small sample size and the potential risk of re-identification of participants from a vulnerable ethnic minority population in a geographically identifiable rural area. De-identified data may be available from the corresponding author upon reasonable request and subject to ethical approval from the Chiang Rai Province Public Health Research Ethics Committee (CRPPHO) and the Taipei Medical University-Joint Institutional Review Board (TMU-JIRB).

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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