NCT06018311Active, not recruiting
Hispanic Adapted and Culturally Relevant Exercising Together
A Pilot Feasibility Study of a Culturally Adapted Partnered Strength Training Intervention for Hispanic Cancer Survivors and Their Caregivers
Source: ClinicalTrials.gov · Last updated 20 Mar 2026
Brief summary (registry, in English)
The purpose of this study is to determine the feasibility and effects of an adapted Exercising Together, a partnered resistance training program, on the physical and mental health of prostate cancer survivors and their informal caregiver. The Exercising Together program is designed to promote teamwork during supervised group exercise classes delivered remotely through videoconferencing software. The intervention period will be 3-months with a 3-month follow-up.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 58 (actual)
- First submitted
- 11 Aug 2023
- Start date
- 1 Nov 2023
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- University of Arizona
- Diseases
- Prostate cancer
- NCT number
- NCT06018311
What you commit to
- Study type: Interventional
- Participants enrolled: 58
- From 1 Nov 2023 to the primary completion date, 31 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- A medical condition, movement or neurological disorder, or medication use that contraindicates participation in moderate intensity exercise or poses a significant safety concern/risk for the well-being of the participant (e.g., declared pregnancy, poorly controlled diabetes, recent cardiac event, neuromuscular disease, untreated orthostatic hypertension, recent surgery, acute hernia, acute rheumatoid arthritis, severe memory disorders, severe balance disorder, severe hearing or vision impairment)
Other
- Cognitive difficulties that preclude answering the survey questions, participating in the exercise classes or performance tests, or providing informed consent as determined by the professional opinion of the Principal Investigator
- Knowingly unable to attend \>75% of the intervention classes due to conflict with the designated time of day, days of the week, and/or location for the exercise class which they initially enrolled
- Incapable of providing informed consent, answering survey questions, participating in the intervention, and following directions during performance testing when English or Spanish language is used
- Unable to be in the same location with participating member during remote exercise classes and performance testing and/or insufficient internet connectivity to support required videoconferencing software
- Phase 2:
Who the study is looking for
- Self-identifies as Hispanic
- Histologically confirmed prostate cancer diagnosis (self-report)
- Completed primary treatment at least 6 weeks prior at time of enrollment
- Has an identified caregiver in any relationship role (e.g., spouse, sibling, parent, friend) who can participate with them.
- 1\. Identifies as an individual (e.g., family member or friend) who provides unpaid care or support to a participating prostate cancer survivor.
- ≥18 years of age
- Understands (ability to read and speak) English or Spanish and able to provide informed consent
- Meets the American College of Sports Medicine pre-participation screening criteria for exercise
- Ability to ambulate (with or without assistive devices)
- Willing to attend study group exercise classes online, complete remote assessments, and answer online surveys
- Has access to a mobile device with camera and internet.
- Able to participate in classes at same time as other participating member.
- Histologically confirmed cancer diagnosis (self-report)
- Completed primary treatment at least 6 weeks prior at time of enrollment
- Has an identified caregiver in any relationship role (e.g., spouse, sibling, parent, friend) who can participate with them.
Criteria the registry did not label
- Phase 1:
Age in the registry: 18 years to 99 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Arizona Cancer Center Coordinator of this site? Confirm its status | Tucson | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.