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Search / Trial NCT06018311

Hispanic Adapted and Culturally Relevant Exercising Together

Launched by UNIVERSITY OF ARIZONA · Aug 29, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Caregivers Cancer Survivorship Hispanic Men'S Health Strength Training Pilot Study

ClinConnect Summary

This clinical trial, called "Exercising Together for Hispanic Prostate Cancer Survivor-Caregiver Dyads," is exploring how a special exercise program can help improve both the physical and mental health of Hispanic men who have survived prostate cancer and their caregivers. The program involves resistance training done in pairs, where survivors and their caregivers can exercise together through live online classes. This study will last for three months, with follow-up assessments taking place three months after the program ends.

To participate, survivors must identify as Hispanic, have been diagnosed with prostate cancer, and completed their primary treatment at least six weeks prior to joining. They also need to have a caregiver who can join them, whether that’s a family member or a friend. Both survivors and caregivers must be at least 18 years old, able to understand English or Spanish, and have access to a device with a camera and internet for the online classes. Participants can expect to engage in group exercise, complete online surveys, and receive support that can help enhance their well-being during and after the program.

Gender

ALL

Eligibility criteria

  • Phase 1:
  • Inclusion Criteria (Survivor only):
  • 1. Self-identifies as Hispanic
  • 2. Histologically confirmed prostate cancer diagnosis (self-report)
  • 3. Completed primary treatment at least 6 weeks prior at time of enrollment
  • 4. Has an identified caregiver in any relationship role (e.g., spouse, sibling, parent, friend) who can participate with them.
  • Inclusion Criteria (Caregivers):
  • 1. Identifies as an individual (e.g., family member or friend) who provides unpaid care or support to a participating prostate cancer survivor.
  • Inclusion Criteria (Survivors and Caregivers):
  • 1. ≥18 years of age
  • 2. Understands (ability to read and speak) English or Spanish and able to provide informed consent
  • 3. Meets the American College of Sports Medicine pre-participation screening criteria for exercise
  • 4. Ability to ambulate (with or without assistive devices)
  • 5. Willing to attend study group exercise classes online, complete remote assessments, and answer online surveys
  • 6. Has access to a mobile device with camera and internet.
  • 7. Able to participate in classes at same time as other participating member.
  • Exclusion Criteria:
  • 1. 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
  • 2. 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)
  • 3. 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
  • 4. 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
  • 5. 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:
  • Inclusion Criteria (Survivor only):
  • 1. Histologically confirmed cancer diagnosis (self-report)
  • 2. Completed primary treatment at least 6 weeks prior at time of enrollment
  • 3. Has an identified caregiver in any relationship role (e.g., spouse, sibling, parent, friend) who can participate with them.
  • Inclusion Criteria for Caregivers remains the same as Phase 1 Exclusion Criteria remain the same as Phase 1

About University Of Arizona

The University of Arizona is a leading research institution dedicated to advancing healthcare through innovative clinical trials and studies. With a strong emphasis on interdisciplinary collaboration, the university leverages its extensive resources and expertise to explore new therapeutic approaches and enhance patient outcomes. Committed to ethical research practices and community engagement, the University of Arizona fosters an environment that promotes scientific discovery and the translation of research findings into clinical applications. Its clinical trial initiatives encompass a wide range of medical disciplines, reflecting the institution's mission to improve health and well-being locally and globally.

Locations

Tucson, Arizona, United States

Patients applied

0 patients applied

Trial Officials

Meghan B Skiba, PhD, MS, MPH, RDN

Principal Investigator

University of Arizona College of Nursing Biobehavioral Health Science Division

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported