Phone-Based wellness program aims to ease breast cancer journey
NCT ID NCT05132296
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a mobile lifestyle program for women with breast cancer who have unhealthy habits. The program offers coaching on diet, exercise, stress management, mindfulness, and sleep. Researchers want to see if it's practical and helps improve quality of life. About 30 women will take part.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2021
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Women with stage I-III BCa scheduled to undergo radiation therapy (RT) or within the first 12 months of having completed primary treatment (they do not need to have undergone RT) * Underwent chemotherapy and surgery * Able to read, write, and speak English * BMI of 25 or higher * 18 years of age or older * Oriented to person, place, and time * Participants must meet at least two of the following criteria related to their lifestyle at the time of diagnosis: * Consume less than 3 servings of fruit and vegetable/day * Engage in less than 75 minutes of moderate/vigorous intensity activity per week, defined as anything that causes small increases in breathing or heart rate for a sustained amount of time (e.g., brisk walking, bicycling) * Engage in a mind-body practice less than 4 times a month * Access to internet connection * Access to a tablet, laptop or computer * Able to come to University of Texas (UT) MD Anderson or Wake Forest for blood collection * Able to perform light physical activity. if any medical issues exist or arise that may limit performing physical activity, a medical release will be required Exclusion Criteria: * Have not completed chemotherapy; have a recurrent BCa diagnosis; another primary cancer diagnosis within past 5 years (not including non-melanoma skin cancers) * Any major thought disorder (e.g., schizophrenia, dementia) * Any major communication barriers that would preclude being able to complete the intervention (e.g., visually or hearing impaired) * Poorly or uncontrolled diabetes in the opinion of the physician(s) * Extreme mobility issues (e.g., unable to get in and out of a chair unassisted)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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M D Anderson Cancer Center
Houston, Texas, 77030, United States
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Wake Forest University Health Sciences
Winston-Salem, North Carolina, 27157, United States
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Other studies related to the condition(s) this trial covers.
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