RECRUITING

Strong Survivors: A Video-assisted Exercise Program for the Geriatric Breast Cancer Patient

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The investigators cancer rehabilitation/recovery program, Strong Survivor, has been designed to be delivered digitally, and while there are many such programs currently available on the internet, especially in the time of COVID-19, the novel feature of this program is the delivery of semi-individualized instruction in real time within a small group setting. The program was designed with physician input and by exercise physiologists and a Doctor of Physical Therapy candidate, all with extensive training in both group and individualized exercise for geriatric and cancer survivor populations. Strong Survivor is 16-week iterative curricular program with three core components: aerobic fitness, balance and mobility, and muscular strength and power. Classes will be held twice per week. The first 4 classes will be deployed in a small class of up to 5 people (first 2 weeks), then one class per week with the small class and one class per week is with a larger class of up to 15 people (weeks 3 and 4). The program is then continued for 12 additional weeks in a larger class using principles and exercises specifically trained during the small group classes. All the exercises offered over the course of the intervention are appropriate for the target population and are standardized so all participants receive the same basic instruction, but level of difficulty is scaled to participant experience, capability, and musculoskeletal limitations. Participants will need to have a minimal adequate space and technology to accommodate this instructional method. Specifically, they will require an internet connected device with a camera that is at least 7 inches square. (tablet size or larger). Additionally, participants' will need to have adequate space to both set up a computer/camera and move around. The minimal acceptable space for this is 6+ feet with an unobstructed view (from a table for instance) of a 2 x 2 open space. All study participants will complete a clinic visit before they join the classes and after the last class to evaluate cardiorespiratory fitness, strength, balance and posture and answer questionnaires about quality of life and system usability.

Official Title

Strong Survivors: A Prospective Study of Video-assisted Exercise Program for the Geriatric Breast Cancer Patient

Quick Facts

Study Start:2025-01-10
Study Completion:2026-12-23
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07071896

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:65 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 65+
  2. 2. Undergone mastectomy within the 4 weeks of being contacted for pre-screening
  3. 3. Own a computer or alternative device capable of real-time Zoom videoconferencing, including access to internet or cellular connectivity sufficient in broadband. This requires a screen of at least 7 inches (a cell phone is large enough for us to see the participant, but not for the participant to see us).
  4. 4. Provision of signed and dated informed consent form
  5. 5. Stated willingness to comply with all study procedures and availability for the duration of the study
  1. 1. Have sustained a previous fall-related fracture within the last 2 years;
  2. 2. have poorly controlled cardiovascular disease, pulmonary disease, or a debilitating musculoskeletal or neurological condition severely limiting function/ability to perform the exercise program as determined by the breast surgeon at screening for trial enrollment
  3. 3. experience vertigo or dizziness/light headedness observed at enrollment or during initial occupational therapy evaluation.
  4. 4. are on multiple benzodiazepine or neuroleptic medications.

Contacts and Locations

Study Contact

Sara M. Grossi, MD
CONTACT
858.249.2764
smgrossi@health.ucsd.edu
Shoshi Barkai, MS
CONTACT
858-534-9315
hbarkai@health.ucsd.edu

Study Locations (Sites)

UCSD
San Diego, California, 92037
United States
UCSD
San Diego, California, 92093
United States

Collaborators and Investigators

Sponsor: University of California, San Diego

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01-10
Study Completion Date2026-12-23

Study Record Updates

Study Start Date2025-01-10
Study Completion Date2026-12-23

Terms related to this study

Keywords Provided by Researchers

  • Exercise, Mastectomy
  • rehabilitation

Additional Relevant MeSH Terms

  • Mastectomy