Virtual Mindful After Cancer (MAC) Intervention to Promote Sexual Health for Breast and Gynecologic Cancer Survivors

Part of paid clinical trials in Corvallis, Oregon.

Sponsor
Oregon State University
Study ID
NCT07055854
Phase
PHASE1
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Mindful After Cancer Program — BEHAVIORAL
    The Mindful After Cancer Program provides education, mindfulness training, and peer support to help cancer survivors navigate sexual and body image concerns.

Study Details

The goal of this study is to plan for a large scale evaluation of a program called Mindful After Cancer, or MAC. The MAC Program provides training in mindfulness, educational material about sexual health after cancer, and support to cancer survivors experiencing sexual and body image concerns. The main study aims are to: 1. Develop effective plans for recruiting participants across multiple sites 2. Evaluate participation in the program and surveys 3. Develop plans to train and supervise the professionals who will deliver the program. Researchers will compare study recruitment across three sites, aiming to identify the most efficient approach for a larger future trial. Participants who are randomly assigned to receive the MAC program will receive access to the 8-week program delivered by a trained mindfulness coach using videoconference and online materials. They will asked to participate in an interview about their experiences at the end of the program. Participants who are not randomly assigned to the MAC program will receive access to the program's educational materials after completing the final survey. All study participants will be asked to complete 3 online surveys. Participants randomly assigned to the MAC Program will also be asked to complete a one-on-one interview about their experience in the program.

Key Dates

Start date
Aug 25, 2025
Status verified
Feb 2026
Primary completion
Nov 30, 2026
Completion
May 31, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • No Intervention: Usual Care
  • Experimental: Intervention

Primary Outcome Measure

Recruitment Accrual Rate- The percent of eligible candidates who enroll [ Time Frame: Baseline ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
Samaritan Pastega Regional Cancer CenterCorvallisOregon97330
Jonathan Wakefield
[email protected]
541-737-1064
Fox Chase Cancer CenterPhiladelphiaPennsylvania19111
Kristen Sorice
[email protected]
215-214-1433
University of PennsylvaniaPhiladelphiaPennsylvania19104
Hannah Toneff
[email protected]
267-882-3186

Find similar trials in Corvallis, OR

By condition
Breast cancer
By specialty
OncologyBreast oncologyWomen's health
By research site
Samaritan Pastega Regional Cancer Center· Corvallis, ORFox Chase Cancer Center· Philadelphia, PAUniversity of Pennsylvania· Philadelphia, PA

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