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NCT Number: NCT07496359

Dyadic Management Intervention in Older People With Co-occurring Cognitive Impairment and Diabetes as a Supplementary Approach to Chronic Diseases Self-Management Program

The goal of this study is to evaluate the effectiveness and implementation of a dyadic management of the Chronic Disease Self-Management Program (CDSMP) for older adults with co-occurring cognitive impairment and diabetes with the involvement of caregivers.

The main questions it aims to answer are:

* Does the intervention improve diabetes self-management and cognitive function in older adults? * How is the implementation of the intervention in real-world settings?

Participants will:

* Attend weekly CDSMP session over a 6-week period (2.5-hour per session). * Provide feedback on their experience with the intervention through interviews and surveys.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Individuals with DM aged >= 55 years old;
  • Recent glycosylated haemoglobin (HbA1c) level of 6.5% or above without change in diabetes medication within the last 3 months based on centre's records;
  • Subjective cognitive decline (using SCDQ21) (separately reported by the patient and/or caregiver) and confirmed by MOCA (Chinese version) screened by the research nurses;
  • Subjects with nominated primary caregivers will be recruited in the intervention group;
  • For caregivers: they will be considered in the project if they have been the primary caregiver for the person for at least 1 year and are providing or involved in the patient's care on a daily basis.

Exclusion criteria

  • Medical diagnoses of dementia;
  • Those who have terminal illness;
  • For caregivers: those who are temporary caregivers and have only provided/involved in care for less than a year.

Treatment and study plan

CDSMP + caregiver support

Behavioral

The CDSMP is an evidence-based program consisting of 2.5-hour sessions held weekly over a six-week period, delivered by two trained leaders per session in person.

Usual Care

Behavioral

Usual care (diabetes education, glucose monitoring and medical consultation)

Primary outcomes

  1. Self-Care of Diabetes Index

    Time frame: From enrollment to 6 months after the intervention begins

    Self-Care of Diabetes Index (SCODI) is a scale, scoring from 0 to 100, where higher scores indicate better self-care for diabetes.

Secondary outcomes

  1. Glycated hemoglobin (HbA1c)

    Time frame: From enrollment to 6 months after the intervention begins

    Glycated hemoglobin (HbA1c) measures average blood sugar levels over the past 2-3 months, acting as a crucial diagnostic and management tool for diabetes. A level below 7% is recommended for patients with diabetes.

  2. Subjective Cognitive Decline Questionnaire 21

    Time frame: From enrollment to 6 months after the intervention begins

    Subjective Cognitive Decline Questionnaire 21 (SCD-Q21) is a reliable, validated 21-item tool designed to detect self-reported cognitive changes, helping distinguish Mild Cognitive Impairment (MCI) from healthy people. The score is from 0 to 21, with a higher score corresponding to a greater likelihood of MCI.

  3. Montreal Cognitive Assessment

    Time frame: From enrollment to 6 months after the intervention begins

    Montreal Cognitive Assessment (MoCA) is a widely used screening scale designed to detect mild cognitive impairment, with scores from 0 to a maximum of 30 points. A higher score on MoCA indicates better cognitive function and less impairment.

  4. Caregiver Contribution to Self-Care of Diabetes Inventory

    Time frame: From enrollment to 6 months after the intervention begins

    Caregiver Contribution to Self-Care of Diabetes Inventory (CC-SCODI) is a validated scale measuring caregiver efforts in diabetes maintenance, monitoring, and management. The score is from 0 to 100 points, with a higher score indicating higher caregiver involvement.

  5. Caregiver Burden Inventory

    Time frame: From enrollment to 6 months after the intervention begins

    Caregiver Burden Inventory (CBI) is a scale measuring multidimensional caregiver burden. Score is from 0 to 96 points, with a higher score indicating higher perceived caregiver burden.

  6. Implementation Outcome: Acceptability of Intervention Measure

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    Acceptability of Intervention Measure (AIM) is a questionnaire assesses how acceptable the intervention is perceived to be by the participants. The total score ranges from 4 to 20, with higher scores indicating greater acceptability of the intervention. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  7. Implementation Outcome: Intervention Appropriateness Measure

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    Intervention Appropriateness Measure (IAM) is a questionnaire evaluates how suitable or relevant the intervention is for the intended purpose or context. The total score ranges from 4 to 20, with higher scores indicating the intervention is perceived as more appropriate. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  8. Implementation Outcome: Feasibility of Intervention Measure

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    Implementation Outcome: Feasibility of Intervention Measure (FIM) is a questionnaire examines how practical and implementable the intervention is in real-world settings. The total score ranges from 4 to 20, with higher scores indicating greater feasibility of implementing the intervention. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  9. Implementation Outcome: Adoption

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    This Adoption questionnaire is derived from the Measuring the Use of the RE-AIM Model Dimension Items Checklist and is designed to assess the adoption of an intervention at both the setting and staff levels. It evaluates factors such as participation rates, reasons for exclusion, and characteristics of participating versus non-participating settings and staff. The measure does not use a specific scoring system; instead, it relies on qualitative and descriptive insights to explore adoption. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  10. Implementation Outcome: Fidelity

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    This Fidelity questionnaire is derived from the Fidelity Checklist for Chronic Disease Self-Management Education Programs and is designed to evaluate the consistency and quality of program implementation. It uses a performance checklist to ensure that the intervention is delivered as intended. The measure does not use a specific scoring system; instead, it relies on qualitative and descriptive insights to explore adoption. If more items on the Fidelity Checklist are met, it indicates better fidelity to the program's design. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  11. Implementation Outcome: Cost

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    This cost outcome focuses on evaluating the economic aspects of the intervention by measuring health-related quality of life using the EQ-5D-5L questionnaire (EuroQol 5-Dimension 5-Level questionnaire), collecting expenditures associated with delivering the intervention (e.g., material costs, staff training, and technical support), and assessing patients' health utilization costs, such as medical expenses, follow-up time, and related financial costs (e.g., transportation). It also considers indirect costs, such as income loss for patients or caregivers, long-term healthcare savings from improved outcomes, and time costs for participants and staff. The collected data will support a cost-effectiveness analysis, providing a comprehensive evaluation of the intervention's value relative to its costs. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  12. Implementation Outcome: Penetration

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    This Penetration questionnaire is derived from the RE-AIM Model Dimension Items Checklist and is designed to evaluate how representative the enrolled patients are of the target population by counting and comparing the number of patients with co-occurring diabetes and MCI who are eligible, invited, excluded, and enrolled to receive CDSMP within participating organizations. Comparisons will be made to non-participants based on key demographic data, including age, diabetes type, MOCA scores and duration, and the number of follow-up attendances. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

  13. Implementation Outcome: Sustainability

    Time frame: From 3 months after the intervention begins to 6 months after the intervention begins

    This Sustainability questionnaire is derived from the RE-AIM Model Dimension Items Checklist and is designed to assess the sustainability of an intervention over time. It includes three key components: Maintenance, which evaluates the long-term impact and continuation of the intervention; Individual Level, which focuses on the persistence of individual behavior changes and health outcomes (e.g., maintaining improvements in quality of life or clinical outcomes at 6 months or more post-intervention); and Setting Level, which examines whether the intervention is institutionalized within the organization, including alignment with the organization's mission, resource allocation, and adaptation for long-term implementation. The measure relies on qualitative and descriptive insights rather than a specific scoring system. Additionally, qualitative interviews with patients and relevant stakeholders are conducted to further evaluate this outcome.

Sponsors and collaborators

Lead sponsor

The Hong Kong Polytechnic University

Other

Registry information

Official study title

Dyadic Management Intervention in Older People With Co-occurring Cognitive Impairment and Diabetes as a Supplementary Approach to Chronic Diseases Self-Management Program: A Hybrid Effectiveness-implementation Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Mar 27, 2026
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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