Recruiting

Supervised Exercise

Sponsor:

Jess S. Gorzelitz

Code:

NCT07765927

Conditions

Breast Cancer

Gynecologic Cancer

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Supervised, Personalized Exercise Program

Study Details

Brief summary:

The purpose of this pilot study is to test a supervised exercise program for adults with a history of breast or gynecologic cancer to see if it is safe, helpful, and easy to take part in.

Conditions

Breast Cancer

Gynecologic Cancer

Study ID

NCT07765927

Start date

Aug 3, 2026

Status verified date

Aug, 2026

Completion date

Apr 15, 2027

Anticipated

Primary completion date

Dec 15, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Age ≥18 years
  • Confirmed diagnosis of breast or gynecologic cancer (any stage)
  • Willingness to participate in the exercise oncology program and associated research procedures Ability to provide informed consent
  • Clearance to participate in exercise as determined by completion of the Physical Activity Readiness Questionnaire Plus (PAR-Q+) and any additional clinical screening as needed

Exclusion Criteria:

  • Presence of absolute contraindications to exercise (e.g., unstable cardiovascular disease, acute illness, or other conditions that preclude safe participation in physical activity)
  • Determination by a referring or treating healthcare provider that the patient is not appropriate for exercise participation at the time of screening
  • Inability to complete required screening procedures, including the PAR-Q+

Study Design

Enrollment

30 participants

Anticipated

Intervention Model

Single group

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Supervised, Personalized Exercise Program

The clinic will conduct comprehensive patient assessments, develop personalized exercise programs, and monitor progress through fitness evaluations and wearable devices.

Interventions

Supervised, Personalized Exercise Program

Sessions will include both resistance (strength) training and aerobic exercise, delivered under the guidance of trained personnel to ensure appropriate technique, progression, and safety.

Primary outcome measure

  • Recruitment rate calculated as the number of participants enrolled divided by the number approached or referred over the study period. [ Time Frame: Recruitment period which will start at day 1 through two months ]
  • Retention rate defined as the proportion of enrolled participants who complete the 12-week intervention and post-intervention assessment. [ Time Frame: Pre-assessment/treatment initiation through post-intervention assessment, approximately 14 weeks ]
  • Adherence to exercise sessions calculated as the number of completed supervised exercise sessions divided by the number of prescribed sessions. [ Time Frame: Pre-assessment/treatment initiation through post-intervention assessment, approximately 14 weeks ]
  • Completeness of functional testing procedures defined as the proportion of participants with complete baseline and follow-up fitness assessments. [ Time Frame: Pre-assessment/treatment initiation through post-intervention assessment, approximately 14 weeks ]

Central Contacts and Locations

Central contacts

Jess Gorzelitz, PhD, MS

(319) 467-0849jessica-gorzelitz@uiowa.edu

Locations

University of Iowa Health Care

Recruiting

Iowa City, Iowa, United States, 52242

Contacts

Jess Gorzelitz, PhD, MS

(319) 467-0849jess-gorzelitz@uiowa.edu

More Information

Sponsor

Jess S. Gorzelitz

Last update posted

Aug 14, 2026

Last verified

Aug, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Jess S. Gorzelitz on 2026-08-14.