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Clinical Trials/NCT02804620
NCT02804620CompletedNot Applicable

From Clinic to Community: Using Peer Support as a Transition Model for Improving Long-term Diabetes-related Health Outcomes

University of British Columbia1 site in 1 country196 target enrollmentStarted: October 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
196
Locations
1
Primary Endpoint
Change in HbA1c%

Study Overview

Brief Summary

This study is a 12-month study. There are two different groups in the study. Both groups will enter the study after the graduation from 8-hour diabetes education course taught at VGH, St. Paul's, or Richmond Hospital. The first group will receive on-going support from their peers who have diabetes and are trained specifically to help other patients with diabetes. The second group will receive the usual care.

Detailed Description

This two-phase study is a randomized controlled trial (RCT) comparing usual care to a 12-month peer-led DSMS intervention designed to improve long-term diabetes-related health outcomes.

In Phase 1, the research team will implement a 30-hour peer leader training (PLT) program recruiting adults with type 2 diabetes and equipping them with the diabetes knowledge, facilitation strategies, and communication skills to deliver a DSMS intervention. In Phase 2, the researchers will conduct the peer support intervention, referred to as the Peer-Led, Empowerment-based Approach to Self-management Efforts in Diabetes (PLEASED). Patients randomized to the PLEASED arm will be paired with a peer leader and receive 12 weekly contacts (face-to-face and telephone support) from their peer leader (PL) in the first 3 months followed by 18 bi-weekly telephone support contacts over the last 9 months.

The goal of the PLEASED intervention is to help patients improve glycemic control and diabetes specific QOL and sustain these health benefits over the long-term. To achieve this goal, PLs will address 3 key functions of peer support that include assisting patients in the daily management of their diabetes, providing social and emotional support, and linking patients to clinical care resources.

Participants' inclusion criteria are: to (1) have type 2 diabetes, (2) be 21 years, (3) speak English or Vietnamese or any languages that their peer leaders speak, (4) be willing to be matched with a peer leader, and (5) have a personal land line telephone or mobile phone.

Peer leaders' inclusion criteria are: (1) have diabetes, (2) be 21 years, (3) speak English, (4) have transportation to attend training, (5) be willing to commit to a 30-hour training program, and (6) have a land line telephone or mobile phone (7) have a self-reported HbA1c of 8% or less.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •for Participants:
  • •To be eligible for the study, patients have to:
  • •have type 2 diabetes,
  • •be 21 years,
  • •speak English or Vietnamese or any languages that their peer leaders speak,
  • •be willing to be matched with a peer leader, and
  • •have a personal land line telephone or mobile phone.

Exclusion Criteria

  • •for Participants:
  • •They should not participate in the study if they have physical limitations, serious health conditions or addictions to alcohol or drugs, which would hinder meaningful participation in the study.
  • •Inclusion Criteria for Peer Leaders:
  • •have diabetes,
  • •be 21 years,
  • •speak English,
  • •have transportation to attend training,
  • •be willing to commit to a 30-hour training program, and
  • •have a land line telephone or mobile phone
  • •have a self-reported HbA1c of 8% or less..
  • •Exclusion Criteria for Peer Leaders:
  • •They should not participate in the study if they have physical limitations, serious health conditions or addictions to alcohol or drugs, which would hinder meaningful participation in the study.

Arms & Interventions

PLEASED

Experimental

The PLEASED intervention arm will receive peer leader who is patients with diabetes that has been gone through our trainings. Also, they will receive three free health screenings (baseline, 3 months, 12 months) and monetary compensation for their time and effort.

Intervention: Peer-led, Empowerment-based Approach to Self-management efforts in Diabetes (Behavioral)

Wait List

No Intervention

The wait list will receive three free health screening (at baseline, 3months, 12 months) and monetary compensation for their time and effort.

Outcomes

Primary Outcomes

Change in HbA1c%

Time Frame: 0, 3, 12 month(s)

Secondary Outcomes

  • ApoB(0, 3, 12 month(s))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tricia Tang

Principal Investigator

University of British Columbia

Study Sites (1)

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