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Hispanic Adapted and Culturally Relevant Exercising Together (HACER)

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University of Arizona

Status

Active, not recruiting

Conditions

Neoplasms
Cancer Survivors
Caregiver Burden
Prostate Cancer
Exercise

Treatments

Behavioral: Exercising together

Study type

Interventional

Funder types

Other

Identifiers

NCT06018311
STUDY00003138

Details and patient eligibility

About

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.

Enrollment

58 patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

58 participants in 1 patient group

Exercising Together
Experimental group
Description:
Dyads perform partnered exercise over 1 hour, 3 days per week in a supervised, group setting remotely for 3 months.
Treatment:
Behavioral: Exercising together

Trial contacts and locations

1

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Central trial contact

Rachel E Jarrett, MPH; Marjorie Barrera

Data sourced from clinicaltrials.gov

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