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"GameDay Ready": Evaluating a Behavioral Weight Management Program for Black Men Living in the Rural South

University of South Carolina logo

University of South Carolina

Status

Completed

Conditions

Physical Inactivity
Obesity
Diet, Healthy

Treatments

Behavioral: GameDay Ready Program

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05530980
Pro00116611
K23MD013899 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The primary objective of this study is to test the feasibility and acceptability of a 12-week behavioral weight management intervention adapted for Black men living in the rural South. The intervention is guided by Self-Determination Theory of Motivation, Social Cognitive Theory, and Ecological Systems Theory. Key aspects of the intervention include a football-themed curriculum, facilitator and peer concordance to the extent possible (ie., similarly aged Black men), an emphasis on male-specific health concerns, group-based competition at multiple levels of the intervention (e.g., during in-person physical activity sessions and for achieving behavioral goals), a limited educational component, and physical activity being a substantial component of meeting sessions.

Enrollment

7 patients

Sex

Male

Ages

25 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Self-identified African American or Black American male
  • BMI 27kg/m^2 to 50kg/m^2 (healthcare provider approval required for those with a BMI >45)
  • Able to speak and understand English

Exclusion criteria

  • Positive response to any question on the Physical Activity Readiness Questionnaire (PAR-Q) (Participant may be included if approval is provided and documented by a healthcare provider)
  • Currently participating in another weight loss trial or program or have participated in a trial or program within 6 months prior to starting the intervention
  • Uncontrolled hypertension (systolic blood pressure ≥160 mm Hg or diastolic blood pressure ≥100 mm hg), diabetes, or asthma (Participant may be included if approval is provided and documented by a healthcare provider)
  • Pulmonary disease requiring supplemental oxygen or daily use of short-acting bronchodilators
  • Any musculoskeletal condition that would preclude meeting recommended levels of moderate-to-vigorous physical activity
  • Within 30 days prior to participating in the intervention, have taken prescription or nonprescription medications, herbals, or supplements for weight loss
  • On special diet for a serious health condition (does not include general dietary advice from a healthcare provider for common risk factors such as hypertension, diabetes, or hyperlipidemia)
  • Major surgery in the past 6 months
  • Have undergone weight loss surgery or considering surgery
  • Have been treated for cancer in the past 12 months (other than non-melanoma skin cancer)
  • Weight loss ≥5% during the past 6 months
  • Any other perceived physical or mental health-related condition that would preclude participating in a behavioral program designed to promote weight loss
  • Intending to move within 6 months

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

7 participants in 1 patient group

GameDay Ready Program
Experimental group
Description:
The GameDay Ready Program is a 12-week, football-themed, behavioral weight management intervention that promotes gradual increases in physical activity, reductions in sedentary time, and improvements in dietary habits through education, self-monitoring of physical activity and diet, personalized goal setting, group-based competition, social support, identifying and overcoming barriers, and including physical activity as a substantial component of meeting sessions. The program is sensitive to unique cultural influences surrounding gender, race, and rurality; and issues related to motivation are threaded throughout the program.
Treatment:
Behavioral: GameDay Ready Program

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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