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Resistance Exercise and Peer Support with Bands/balls and Digital Support Among Women with Polycystic Ovary Syndrome

Personalized Resistance Training with Peer Support for Women with PCOS Using a Smart Home Video Device: Feasibility Study Guided by Self-Determination Theory

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06629883
Acronym
REPS w/BANDS
Enrollment
10
Registered
2024-10-08
Start date
2022-06-01
Completion date
2023-05-31
Last updated
2024-10-08

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

Conditions

Polycystic Ovary Syndrome (PCOS)

Keywords

polycystic ovary syndrome, motivation, resistance training, digital technology, proof of concept study, feasibility studies

Brief summary

The purpose of this one arm pilot was to assess the feasibility and acceptability of REPS w/BANDS and evaluate for signals of improvement for depressive symptoms, anthropometrics, and muscular endurance. Participants completed a 12-week personalized in-home resistance exercise program that was delivered in real-time via a smart home video device along with a buddy system for peer support.

Detailed description

Research findings reveal that women with polycystic ovary syndrome (PCOS) report low exercise motivation due to PCOS stigma-related stress and lack of social connection, thus inhibiting exercise in public and group settings. The purpose of this study was to implement and assess the feasibility and acceptability of an in-home personalized resistance exercise (RE) program delivered in real time by a smart home video device (SHVD) with peer support provided by a buddy system. This theory-informed, one-arm proof-of-concept study provided participants (n=10) with an SHVD, exercise equipment (exercise bands, stability ball), and 2 supervised RE sessions per week for 12 weeks via the SHVD's video feature and incorporated strategies from self-determination theory to meet the psychological needs of autonomy, competence, and relatedness. Participants were randomly paired with a buddy. Feasibility, acceptability, depressive symptoms, anthropometrics, and muscular endurance were measured using surveys, fitness testing, and interviews. Quantitative data were calculated using t-tests. Qualitative data were analyzed via thematic analysis.

Interventions

BEHAVIORALREPS w/BANDS

This theory-informed, one-arm proof-of-concept study provided participants (n=10) with an SHVD, exercise equipment (exercise bands, stability ball), and 2 supervised RE sessions per week for 12 weeks via the SHVD's video feature and incorporated strategies from self-determination theory to meet the psychological needs of autonomy, competence, and relatedness. Participants were randomly paired with a buddy.

Sponsors

University of South Carolina
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* an age of 18 or older * a confirmed PCOS diagnosis by a healthcare provider * physical activity readiness as determined by the Physical Activity Readiness Questionnaire (PAR-Q) * residence within driving distance of the main university campus.

Exclusion criteria

* cardiorespiratory disease (e.g., congestive heart failure) * hypertension * orthopedic injury (e.g., herniated disc) * pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
RecruitmentAt the end of 12 weeksScreened participants # / Enrolled participants #
AttendanceAt the end of 12 weeksSession # attended / Session # prescribed
RetentionAt the end of 12 weeksParticipant # completing 2nd assessment / Participant # completing baseline assessment
Acceptability InterviewsAt the end of 12 weeksAcceptability was measured via content analysis of participant interviews
Acceptability Likert ScalesAt the end of 12 weeksQuestions of about satisfaction with REPS w/BANDS were scored on a scale of 0-4, with O indicating poor and 4 indicating excellent.

Secondary

MeasureTime frameDescription
Modified Push Up TestAt baseline and at the end of 12 weeksUpper body muscular endurance was measured with this test. The score was the number of correctly performed push-up in one minute.
Depressive SymptomsFrom baseline and at the end of 12 weekshe Personal Health Questionnaire (PHQ-8) was used to assess prevalence and severity of depressive symptoms occurring within the past two weeks. The score is the sum of the 8 items. 0-4 = minimal or no depression, 5-9 = mild depression, 10-14 = moderate depression, 15-19 = moderately severe depression, 20-24 = severe depression
Curl Up TestAt baseline and at the end of 12 weeksThis test was used to measure muscular endurance of the core. The score was the number of curl up properly performed to a cadence of 40bpm.
BodyweightAt baseline and at the end of 12 weeksParticipants self-reported body weight in pounds during the fitness assessments.
HeightAt baseline and at the end of 12 weeksParticipants self-reported height in feet and inches during the fitness assessments.
Waist CircumferenceAt baseline and at the end of 12 weeksParticipants were guided to measure waist circumference in inches during the fitness assessments.
Squat TestAt baseline and at the end of 12 weeksLower body muscular endurance was measured using the squat test. The score was the number of squats performed with proper form.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 22, 2026