Wellness Engagement Project, Petersburg (WE)

Virginia Commonwealth University (VCU)

Status: Terminated

Conditions: Obesity

Treatments: Behavioral: Wellness Engagement Program

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT02652845

1R24MD008128 (U.S. NIH Grant/Contract)

5R24MD008128

Details and patient eligibility

About

This study tests the feasibility of a health and wellness trial designed with community input. This 12-week program will be tested over a 24-week period using a delayed treatment control group.

Full description

This 12-week program was designed based on input from Petersburg, VA community residents, collected through various methods over a two-year period. The 12 week program is designed to impact three levels: individual, family and community. At the individual level, participants receive print material lessons related to healthy eating and increasing physical activity, as well as videos that model these lessons; participants will also have access to a peer support coach who will contact them on a biweekly basis and are trained to help them identify and reach their own personal health goals. At the family level, participants are encouraged to share all of the information they receive as a part of this program with the rest of their family, and are asked to begin walking regularly and to attend fitness and nutrition classes held within their neighborhood (by the WE program) with family members. On a community level, local church groups and neighborhood organizations will receive assistance in launching walking clubs, and all community residents are invited to attend the physical activity and nutrition classes that the WE project hosts within the community.

Enrollment: 20 patients

Sex: All

Ages: 12 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age between 18-65 years.
• Must have a school going child between 12-17 living in the home.
• BMI between 25 and 50 kg/m2.

Exclusion criteria

• report not being able to walk 2 blocks (1/4 mile) without stopping
• currently participating in another weight loss program
• taking a weight loss medication
• have a history of bariatric surgery
• pregnant or plan to become pregnant during the intervention timeframe
• report an unsupervised heart condition, chest pain during periods of rest or activity, or loss of consciousness on the Physical Activity Readiness Questionnaire
• report a medical condition that would jeopardize their safety if involved in a weight management program with diet and exercise guidelines (e.g., uncontrolled heart problem)
• fail medical screening by study medical staff)
• report conditions that, in the judgment of the PI, would render the participant unlikely to follow the study protocol (e.g., planned move from the area, dementia, substance abuse).

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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20 participants in 2 patient groups

Intervention-Wellness Engagement Program

Experimental group

Description:

The group assigned to the intervention arm will receive treatment as described below for a twelve week period: Weekly lessons related to healthy eating and physical activity Biweekly check-in calls with a trained peer support coach Access to neighborhood wide physical activity and nutritional education events

Treatment:

Behavioral: Wellness Engagement Program

Delayed treatment control group

No Intervention group

Description:

The delayed treatment control group will not receive the intervention for measurement purposes; however the intervention as described will be administered to this group upon conclusion of the 12 week period for the intervention group.