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Mind-Body Interventions for the Improvement of Quality of Life, Stress, and Sleep Quality Among Survivors of Breast, Prostate, Endometrial, or Colorectal Cancer

Influence of Mind-Body Interventions on Cancer-Related Symptom Management in Survivors

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07745023
Enrollment
30
Registered
2026-08-04
Start date
2026-09-30
Completion date
2029-02-02
Last updated
2026-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Stage I, Colorectal Cancer

Brief summary

This clinical trial studies how well mind-body interventions work in improving quality of life (QOL), stress, and sleep quality among survivors of breast, prostate, endometrial, or colorectal cancer. For many cancer survivors, the experience of cancer extends well beyond the completion of therapy. Common long-term effects include fatigue, cognitive impairment, anxiety, depression, sleep disturbance, and diminished physical function, all of which contribute to reduced QOL and overall health. Yoga, a mind-body intervention, utilizes breathwork, meditation, and gentle movement to help reduce activity in the body's nervous system. Breathwork and meditation have been shown to improve heart rate variability (a measure of the body's ability to adapt to stress). Movement-based practices may offer added benefit by supporting coordination and physical resiliency, aspects that are often reduced after cancer treatment and can lead to decreased QOL. This trial may help researchers determine whether a mind-body intervention that includes breathwork and meditation, as well as an intervention that includes breathwork and meditation plus gentle movement can work to improve QOL, stress, and sleep quality among survivors of breast, prostate, endometrial, or colorectal cancer.

Detailed description

PRIMARY OBJECTIVE: I. Pilot test video and/or audio content consisting of six, 15-minute breathwork and meditation videos/audio, and six, 15-minute guided, gentle movement videos developed for this intervention for feasibility and acceptability, and provide preliminary data on QOL in cancer (breast, colon, endometrial, and prostate) survivors using patient-reported outcomes measurements completed at pre- and post- intervention. SECONDARY OBJECTIVES: I. Evaluate program satisfaction using structured questionnaires for all participants at post-intervention. II. Identify perceived barriers, evaluate facilitators, and identify recommendations for future scaling and delivery in varied survivorship settings r.

Interventions

OTHERMedia Intervention

View breathwork and meditation videos

Complete breathwork exercises

Complete Meditation exercises

Sponsors

Roswell Park Cancer Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Received a diagnosis of invasive, non-metastatic breast, colorectal, endometrial, or prostate cancer within the past 12 months * Have completed active anti-cancer therapy (hormonal, bisphosphonate, or androgen therapy is allowed) * Able to safely participate in light-weight physical activity (e.g. gentle yoga)

Exclusion criteria

* Individuals with skeletal instabilities, cardio-pulmonary comorbidities, or other conditions that may preclude safe participation in light physical activity * Pregnant or nursing female participants * Unwilling or unable to follow protocol requirements * Any condition that, in the Investigator's opinion, deems the participant an unsuitable candidate * Unable to complete survey questionnaires in English

Design outcomes

Primary

MeasureTime frameDescription
Change in quality of lifeBaseline up to 6 weeksPatients view guided breathwork, meditation, and gentle yoga movement videos and complete these exercises over 30 minutes weekly for 6 weeks on study. Patients also wear an activity tracker throughout the study

Secondary

MeasureTime frameDescription
Adherence RateUP to 6 weeksProportion of participants who complete at least 80% of the assigned interventions

Contacts

CONTACTKathryn G Glaser
AskRPCI@roswellpark.org716*845-2300

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 5, 2026