A Trial of Incentives and Peer Mentors to Improve Diabetic Outcomes

NCT ID: NCT01125969

Last Updated: 2018-08-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

240 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-03-31

Study Completion Date

2016-12-31

Brief Summary

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In recent years, social networks have garnered attention in both academic journals and the lay press because of strong associations demonstrated in retrospective studies between social networks and incidence of major health problems such as obesity and smoking. Financial incentives have also been demonstrated to improve health behaviors in obesity, smoking, and medication adherence. We propose to conduct a randomized controlled trial among a predominantly African American population with persistently poor diabetes mellitus (DM) control to examine whether two novel interventions, lottery based financial incentives and telephone based one-on-one peer mentoring (the 'buddy system'), can significantly ameliorate disparities in poor DM control.

The intervention is based on epidemiologic evidence, randomized controlled trials, and pilot studies demonstrating: 1) Lottery based financial incentives are a powerful motivator of behavior change; 2) One-on-one peer mentoring is a flexible, cost-efficient means of increasing DM specific social support and may be particularly salient in minority communities; and 3) Matching patients with poorly controlled DM with a similar individual from their community who has gained control of their DM draws on existing community assets in creating an inherently culturally competent intervention. DM patients with poor DM control will be randomized to 1 of 4 arms: usual care; telephone based one-on-one peer mentoring; lottery based financial incentives; and peer mentoring plus financial incentives.

The Specific Aims are to test: 1) The effectiveness of telephone based one-on-one peer mentoring in improving glycemic control relative to usual care; 2) The effectiveness of lottery based financial incentives in improving glycemic control relative to usual care; 3) The effectiveness of combining peer mentoring and financial incentives relative to control; and 4) The relative cost effectiveness of all four approaches. In exploratory analyses, we will examine whether African American patients enrolled in intervention arms have greater improvement in glycemic control than white patients, whether intervention group patients experience greater improvements in blood pressure (BP) and lipid control, and whether peer mentors experience improvements in their own health. We will pair mentors with mentees based on race, gender, age, and disease severity. The active intervention will be run for a 6-month time period, with participants followed for an additional 6 months to determine if effects persist post intervention.

The proposed interventions address multiple barriers to effective disease management common among patients with DM. If effective, these interventions could provide important models for improving glycemic control in general and, in particular, for addressing racial disparities in DM outcomes.

Detailed Description

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Conditions

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Diabetes Mellitus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Control

Group Type ACTIVE_COMPARATOR

Education

Intervention Type BEHAVIORAL

Standard brochure about improving blood sugar control plus warnings about dangers of persistently high sugars and hypoglycemia

Incentive

Group Type EXPERIMENTAL

Incentives

Intervention Type BEHAVIORAL

Incentives will be offered for checking blood glucose each morning and for control of blood glucose (between 80-140 mg/dL).

Education

Intervention Type BEHAVIORAL

Standard brochure about improving blood sugar control plus warnings about dangers of persistently high sugars and hypoglycemia

Peer Mentoring

Group Type EXPERIMENTAL

Education

Intervention Type BEHAVIORAL

Standard brochure about improving blood sugar control plus warnings about dangers of persistently high sugars and hypoglycemia

Peer mentoring

Intervention Type BEHAVIORAL

Participant is assigned a peer mentor who is matched on gender, race and age and who achieved good glucose control after previously having poor glucose control.

Incentives and Peer Mentoring

Group Type EXPERIMENTAL

Incentives

Intervention Type BEHAVIORAL

Incentives will be offered for checking blood glucose each morning and for control of blood glucose (between 80-140 mg/dL).

Education

Intervention Type BEHAVIORAL

Standard brochure about improving blood sugar control plus warnings about dangers of persistently high sugars and hypoglycemia

Peer mentoring

Intervention Type BEHAVIORAL

Participant is assigned a peer mentor who is matched on gender, race and age and who achieved good glucose control after previously having poor glucose control.

Interventions

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Incentives

Incentives will be offered for checking blood glucose each morning and for control of blood glucose (between 80-140 mg/dL).

Intervention Type BEHAVIORAL

Education

Standard brochure about improving blood sugar control plus warnings about dangers of persistently high sugars and hypoglycemia

Intervention Type BEHAVIORAL

Peer mentoring

Participant is assigned a peer mentor who is matched on gender, race and age and who achieved good glucose control after previously having poor glucose control.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* diagnosed with diabetes mellitus
* 30 to 70 years old
* persistently poor glucose control, defined as having the last two HbA1c values \> 8%, with at least one measure within 3 months of enrollment
* receiving treatment for diabetes mellitus at one of five University of Pennsylvania outpatient clinics

Exclusion Criteria

* does not speak English
* unable to provide informed consent
Minimum Eligible Age

30 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Michigan

OTHER

Sponsor Role collaborator

University of Pennsylvania

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Judith A. Long, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

Locations

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University of Pennsylvania

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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10022605

Identifier Type: -

Identifier Source: org_study_id

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