Testing the Efficacy of a Spousal Support Enhanced Weight Loss Program on Weight Loss Among African American Men

NCT02458053 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 104

Last updated 2017-09-14

No results posted yet for this study

Summary

The purpose of this study is to determine the effect of a spousal support enhanced weight loss program on weight loss among African American men.

Conditions

Interventions

BEHAVIORAL

Attends with partner

The index partner will participate in intervention as a couple with their female counterpart.

BEHAVIORAL

Couples Skill Training

Participants and their partners will attend a pre session covering topics to assist them in working together to facilitate lifestyle changes.

BEHAVIORAL

Face to face group sessions

Group sessions will consists of components in traditional weight management programs.

BEHAVIORAL

Self Monitor

Participants will be instructed to monitor their eating and physical activity behaviors online/mobile application.

OTHER

Notebook

The notebook will consist of behavioral lessons, diet and physical activity plans, and additional resources to assist participants in achieving their behavioral goals.

BEHAVIORAL

Feedback

Each participant will receive a tailored email providing feedback on their weekly progress.

Sponsors & Collaborators

  • University of North Carolina, Chapel Hill

    lead OTHER

Principal Investigators

  • Deborah F Tate, PhD · University of North Carolina, Chapel Hill

  • Candice Alick, MS · University of NC-Chapel Hill

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2016-12-31
Completion
2017-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02458053 on ClinicalTrials.gov