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CompletedNCT02661581PLEASEDUpdated Dec 5, 2024

Peer-led, Empowerment-based, Approach to Self-management Efforts in Diabetes

An interventional study of Peer Support in Diabetes, sponsored by University of British Columbia. Completed at 1 site in Canada. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2024-12-05.

Sponsored by University of British Columbia · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
114
Allocation
Non-randomized
Ages
21 Years and older
Sex
All
01

Study summary

PLEASED is a 12-month program that aims to help South Asians with type 2 diabetes improve and sustain diabetes-related health outcomes e.g. glycemic control, quality of life...) achieved from previous short-term diabetes education program. Our goal is to provide a new generation of education and support that can be ongoing, patient-driven, and flexible to the dynamic and evolving conditions of patients' "real-word" environment and life circumstances.

Read the detailed description

Diabetes self-management education: In the first three months of PLEASED, patients with type 2 diabetes will participate in 12 weekly sessions: 6 sessions will focus on diabetes education and be delivered by a health professional and 6 sessions will focus on lifestyle change and be delivered by a peer leader. Education sessions will be 2-hours long and be facilitated by nurses, dieticians, and pharmacists. Patients will learn about the diabetes disease process, lifestyle modification, healthy eating, physical activity, medications, monitoring, short- and long- complications, diabetes distress, and coping. Lifestyle change sessions will be 1-hour long and start with 30 minutes of physical activity followed by 30 minutes of goal-setting, action planning, and problem solving. Additional activities such as recipe makeovers and exchanges will also be included.

Diabetes self-management support: In the next nine months of the PLEASED program, patients will be invited to attend 32 weekly self-management support sessions (1-hour long) facilitated by a peer leader. The goal of these sessions is to help patients continue making positive lifestyle changes. Each support session will start with 30 minutes of physical activity led by the peer leader followed by a discussion where participants are invited to (1) discuss self-management challenges, (2) share thoughts and feelings about these challenges, (3) ask self-management questions, (4) engage in problem solving, and (5) set self-management goals and design behavioral experiments to achieve those goals. Patients are invited to attend as frequently as they need or as they are able to given other competing life demands. While these sessions focus on lifestyle change and emotional support, participants will be able to obtain responses to medical and clinical questions from 811 or the PLEASED hotline (hosted by dieticians, nurses, and pharmacists).

All patients enrolled in the PLEASED program will undergo three free health assessments: at the start of the program, at 3 months, and at 12 months. Health assessments will include measuring glycemic control, ApoB, blood pressure, waist circumference, weight, and body mass index. All patients will also complete a survey assessing quality of life, social support, depression, and self-efficacy.

02

Conditions studied

  • Diabetes

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Keywords

  • Diabetes
  • Peer Leader Support
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 114 is above the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

University of British Columbia is the lead sponsor of 1,309 studies on the registry; 253 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 1 (17%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

To be eligible to participate as a subject in this study, individuals must

  1. Have type 2 diabetes,
  2. Be of South Asian background,
  3. Live in the Metro Vancouver area,
  4. Be at least 21 years old,
  5. Have transportation to attend group sessions.

To be eligible to participate as a peer leader in this study, individuals must

  1. Have diabetes or are a caregiver to someone who has diabetes,
  2. Are of South Asian background,
  3. Live in the Greater Vancouver area,
  4. Are at least 21 years old,
  5. Are bilingual in English and Punjabi,
  6. Have transportation to attend training,
  7. Are able and willing to commit to 6 sessions of training (5 hours each, over a 6 week period)

Exclusion criteria for both participants and peer leaders include:

  1. Serious health conditions
  2. Addictions to alcohol or drugs, which would hinder meaningful participation in the study.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
114 participants (actual)

Study arms

  • Experimental
    Peer Support

    Peer support intervention group: During the first 3 months of DSME, participants in the DSMS intervention group will be invited to attend 6 lifestyle change sessions delivered a 2-person peer leader team and conducted bi-weekly. Immediately following the 3 months of DSME, participants are invited to attend 9 months of weekly DSMS sessions (60-minutes per session) delivered by a Peer Leader. These sessions are designed to sustain the self-management gains achieved in the 3 months of DSME.

    Behavioral: Peer Support

  • No intervention
    Control

    Immediately following the 6 bi-weekly DSME sessions, participants randomized to the control group will have completed their participation in the study.

Interventions

  • BehavioralPeer Support

    The intervention is lifestyle change. First, the peer leaders will be trained how to conduct diabetes self-management education and support sessions. During the first 3 months, all the participants will attend the diabetes self-management education sessions. The participants in the intervention arm will also receive diabetes self-management support sessions as well. In the end of the first 3 months, the intervention group participants will receive weekly support sessions for 9 months.

06

What researchers measure

Primary outcomes

  1. Glycemic Control measured by HbA1c

    To compare a peer support model for diabetes self-management support (DSMS) to usual care on sustaining improvements in glycemic control achieved from short-term diabetes self-management education (DSME).

    Time frame: Up to 12 months

Secondary outcomes

  1. Blood pressure (mmHg) measured by Omron BP785 monitor

    Time frame: Up to 12 months

  2. ApoB (g/L) will be collected using venous puncture blood draw

    Time frame: Up to 12 months

  3. Waist circumference (inch) measured by Seca 203 Circumference Measuring Tape

    Time frame: Up to 12 months

  4. Body Mass Index (kg/m2)

    Time frame: Up to 12 months

  5. Physical activity measured by the actical accelerometer

    Time frame: Up to 12 months

  6. Diabetes-specific Social Support will be assessed using a 4-item perceived social support scale developed by Tang et al. that measures amount of support and satisfaction with support from family, friends and the health care team

    Time frame: Up to 12 months

  7. Depressive Symptom Severity will be assessed with the PRIME-MD Patient Health Questionnaire (PHQ-9)

    Time frame: Up to 12 months

  8. Diabetes-related distress measured by the Diabetes Distress Scale (DDS), a 17-item scale developed by Polonsky and colleagues

    Time frame: Up to 12 months

  9. Height measured using a stadiometer

    Time frame: Up to 12 months

  10. Weight measured on a high quality, calibrated digital scale, with the participant wearing clothes, but no shoes

    Time frame: Up to 12 months

07

Study locations

1 site
  • St. Paul's Hospital
    Vancouver, British Columbia V6Z 1Y6, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02661581
Lead sponsor
University of British Columbia
Collaborators
VGH and UBC Hospital Foundation
Responsible party
Tricia Tang (Principal Investigator, University of British Columbia) — Principal investigator
First posted
Jan 22, 2016
Start date
Nov 2013
Primary completion
Sep 2017
Completion
Sep 2017
Last update
Dec 5, 2024

Study contacts

Tricia Tang, PhD
principal investigator · University of British Columbia

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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