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A Resistance Training Program for Black Women: Project F.I.R.E.

A Resistance Training Program for Black Women: Project F.I.R.E.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05733260
Enrollment
30
Registered
2023-02-17
Start date
2023-03-01
Completion date
2023-12-01
Last updated
2023-03-06

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

Conditions

Obesity

Brief summary

This study will utilize a randomized control trial design, with participants randomly assigned to a theoretically-based culturally tailored intervention or standard of care group. Baseline (Week 0), 12-week, and 3-month follow-up (Week 24). Body composition and adherence will be tracked throughout the study. The exercise intervention will include a total body resistance training protocol and will take place at local fitness center. Participants will be randomized to either the theoretical-based culturally tailored intervention group or the standard exercise group in which each will be facilitated and supervised by a Black-trained research personnel following culturally tailored recommendations. All participants will attend a 10-week resistance training program twice per week for a total of 20 sessions from Weeks 2-11. Week 1 will be used to familiarize the participants with the resistance training exercises. Those randomized to the culturally tailored intervention group will receive health education, weekly text messages and self-regulatory strategies to overcome barriers to exercise. Participants will return for post testing at weeks 12 and 24.

Detailed description

This study will utilize a randomized control trial design, with participants randomly assigned to a theoretically-based culturally tailored intervention or standard of care group. Baseline (Week 0), 12-week, and 3-month follow-up (Week 24). Body composition and adherence will be tracked throughout the study. The exercise intervention will include a total body resistance training protocol and will take place at local fitness center. Participants will be randomized to either the theoretical-based culturally tailored intervention group or the standard exercise group in which each will be facilitated and supervised by a Black-trained research personnel following culturally tailored recommendations. All participants will attend a 10-week resistance training program twice per week for a total of 20 sessions from Weeks 2-11. Week 1 will be used to familiarize the participants with the resistance training exercises. Those randomized to the culturally tailored intervention group will receive health education, weekly text messages and self-regulatory strategies to overcome barriers to exercise. Participants will return for post testing at weeks 12 and 24.

Interventions

BEHAVIORALExercise

10 weeks of resistance training.

Sponsors

Auburn University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 34 Years
Healthy volunteers
Yes

Inclusion criteria

* 18 and 34 years * Identify as a black female * Not actively participating in some type of exercise on a regular basis (at least three days a week for the past three months) * Low risk for medical complications from exercise (as determined by the PAR-Q), * Not pregnant or planning to become pregnant throughout the duration of the study * Must live, work, or be a student in the city of Auburn, AL

Exclusion criteria

* women over 35 * Women who do not identify as black * Regular exercisers, * Pregnant women * Women who do not have residency within Auburn AL

Design outcomes

Primary

MeasureTime frameDescription
Body Composition12 weeksChanges in body fat percentage assessed by dual x-ray absorptiometry

Secondary

MeasureTime frameDescription
Adherence to resistance training12 weeksThe number of days resistance training is completed each week.

Contacts

Primary ContactDanielle D Wadsworth, Ph.D.
wadswdd@auburn.edu3348441836

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026