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Together Everyone Achieves More (TEAM) Trial

The Together Everyone Achieves More Physical Activity Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05519696
Acronym
TEAM
Enrollment
360
Registered
2022-08-29
Start date
2022-09-12
Completion date
2026-12-31
Last updated
2024-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Activity

Keywords

African American women, Community-Based Intervention, Social Environment

Brief summary

The Together Everyone Achieve More (TEAM) Physical Activity trial evaluates the efficacy of a group-based social affiliation intervention (vs. a standard group-delivered physical activity comparison program) for increasing physical activity among inactive African American women. Using a group cohort randomized design implemented at community centers across five years, the primary aim of this study is to evaluate the efficacy of the 10-week TEAM-PA group-based intervention (vs. comparison program) on increasing daily total physical activity from baseline to post-intervention and maintenance at a 6-month follow-up.

Interventions

BEHAVIORALIntervention

Participants receiving the intervention will complete a 10-week group program. Group sessions meet once per week for 2 hours and include three components - discussion-based health promotion initiative, team-based physical activity games/activities, and team-based goal-setting and behavioral skills training. The health promotion initiative uses cultural targeting and includes a focus on cultural topics related to collectivism. Participants receive FitBits to track their physical activity and through the FitBit mobile app are connected to their group members to encourage communication and social support.

BEHAVIORALComparison

Participants receiving the comparison program will complete a 10-week group program. Group sessions meet once per week for 2 hours and include three components - discussion-based health promotion initiative, group walking program, and individual-based goal-setting and behavioral skills training. The health promotion initiative uses cultural targeting only (and no focus on collectivism). Participants receive FitBits to track their physical activity, but are not connected to their group members on the mobile app.

Sponsors

University of South Carolina
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

All measurement staff will be blind to treatment condition

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* at least 18 years of age * self-identifying as an African American or Black female * engaging in \< 60 minutes of moderate to vigorous physical activity per week for the last three months

Exclusion criteria

* having a cardiovascular or orthopedic condition that would limit physical activity (including walking with a cane/walker) * currently pregnant or planning to become pregnant in the next 2 months * uncontrolled blood pressure (systolic \>180 mmHg/diastolic \> 110 mmHg)

Design outcomes

Primary

MeasureTime frameDescription
Total Physical ActivityBaseline, post-intervention (10 weeks), and 6 months post-interventionAverage minutes of total physical activity (PA) per day; Objective assessments of total PA will be obtained with ActiGraph accelerometers. Participants will wear the monitor on the non-dominant wrist for 7 consecutive days. The investigators will evaluate whether there is a change in minutes of total PA per day from baseline to 10 weeks and maintenance at 6 months post-intervention, and whether there are group differences between the intervention and comparison programs.

Secondary

MeasureTime frameDescription
Light Physical ActivityBaseline, post-intervention (10 weeks), and 6 months post-interventionAverage minutes of light physical activity (PA) per day; Objective assessments of light PA will be obtained with ActiGraph accelerometers. The investigators will evaluate whether there is a change in daily minutes of light PA from baseline to 10 weeks and maintenance at 6 months post-intervention, and whether there are group differences between the intervention and comparison programs.
Percentage meeting national guidelines for weekly moderate to vigorous physical activityBaseline, post-intervention (10 weeks), and 6 months post-interventionPercentage of participants with at least 150 minutes of moderate physical activity and/or 75 minutes of vigorous physical activity per week; Objective assessments of minutes of moderate to vigorous physical activity will be obtained with ActiGraph accelerometers. The investigators will evaluate whether there is a change in the percentage of participants meeting national guidelines from baseline to 10 weeks and maintenance at 6 months post-intervention, and whether there are group differences between the intervention and comparison programs.
Sedentary BehaviorBaseline, post-intervention (10 weeks), and 6 months post-interventionAverage minutes of sedentary behavior per day; Objective assessments of sedentary behavior will be obtained with ActiGraph accelerometers. The investigators will evaluate whether there is a change in sedentary behavior from baseline to 10 weeks and maintenance at 6 months post-intervention, and whether there are group differences between the intervention and comparison programs.
Body Mass Index (BMI)Baseline, post-intervention (10 weeks), and 6 months post-interventionHeight (cm) and weight (kg) will be measured using a stadiometer and medical-grade scale. Scores will be used to calculate BMI (kg/m\^2). The investigators will evaluate whether there is a change in BMI from baseline to 10 weeks and maintenance at 6 months post-intervention, and whether there are group differences between the intervention and comparison programs.
Blood PressureBaseline, post-intervention (10 weeks), and 6 months post-interventionSystolic and diastolic blood pressure will be measured using an automatic blood pressure machine. The investigators will evaluate whether there is a change in blood pressure from baseline to 10 weeks and maintenance at 6 months post-intervention, and whether there are group differences between the intervention and comparison programs.
Two-Minute Walk Test (Walking Speed)Baseline, post-intervention (10 weeks), and 6 months post-interventionStarting from a standing position, participants are asked to walk as far as they can in a safe manner for two minutes over a flat out and back 50 feet course. The distance traveled to the nearest foot is recorded.

Other

MeasureTime frameDescription
Group Interactions (Communication, Cooperation, Friendly Competition)Baseline, post-intervention (10 weeks), and 6 months post-interventionItems developed by Harden et al (2014) \[12 items; 1 = Strongly Disagree, 6= Strongly Agree\] will be used to assess communication, cooperation, and friendly competition among group members. Mean composite scores will be calculated (ranging from 1-6), with higher numbers indicate more positive group interactions.
Collective Efficacy for Physical Activity among Group MembersBaseline, post-intervention (10 weeks), and 6 months post-interventionThe Unity subscale from the Collective Efficacy Questionnaire for Sports (Short et al. 2005) will be adapted \[4 items; 5-point, 1 = Not at all confident, 5 = Extremely confident\] to assess collective efficacy for physical activity among group members. A mean composite score will be calculated (ranging from 1-5), with higher numbers indicating greater collective efficacy.
Relatedness among Group MembersBaseline, post-intervention (10 weeks), and 6 months post-interventionThe Need for Relatedness Scale (Richer & Vallerand, 1998) will be used \[10 items; 1 = Strongly Disagree, 6= Strongly Agree\] to assess relatedness among group members. A mean composite score will be calculated (ranging from 1-6), with higher numbers indicating greater relatedness.
Group Cohesion among Group MembersBaseline, post-intervention (10 weeks), and 6 months post-interventionTwo subscales (Individual Attraction to the Group - Social; Group Integration - Social) from the Physical Activity Group Environment Questionnaire (Estrabrooks et al 2000) \[10 items; 1 = Strongly Disagree, 6= Strongly Agree\] will be used to assess group cohesion among group members. Mean composite scores will be calculated (ranging from 1-6), with higher numbers indicate greater group cohesion.
Reciprocal Social Support for Physical ActivityBaseline, post-intervention (10 weeks), and 6 months post-interventionThe Support for Exercise Scale (Sallis et al 1987) will be adapted \[12 items; 1 = Never; 6 = Very Frequently \] to measure providing and receiving of social support among group members. Mean composite scores will be calculated (ranging from 1-6), with higher numbers indicate greater social support.

Countries

United States

Contacts

Primary ContactAllison Sweeney, PhD
sweeneam@mailbox.sc.edu803-576-7891

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026