Telehealth Intervention for Symptom Management and Adherence to Adjuvant Endocrine Therapy (NCT07759947) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Telehealth Intervention for Symptom Management and Adherence to Adjuvant Endocrine Therapy
United States400 participantsStarted 2027-02-01
Plain-language summary
The goal of this study is to demonstrate the efficacy of an evidence-based, small-group, telehealth intervention ('STRIDE') for improving patients' ability to cope with side effects from adjuvant endocrine therapy (AET) and adhere to AET medication regimens for patients with hormone-sensitive breast cancer.
Who can participate
Age range
21 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Female ≥ 21 years old
* Diagnosis of early-stage (0-IIIb), hormone receptor positive (ER+/PR+) breast cancer
* Completed primary treatment (surgery, chemotherapy, and/or radiation)
* Within 3 to 12 months of starting oral adjuvant endocrine therapy (AET)
* Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
* Ability to read and respond in English or Spanish
* Distress about AET ≥ 4 on a 0-10 scale
Exclusion Criteria:
* Cognitive impairment, uncontrolled psychosis, or serious mental illness prohibiting participation in the study as per the judgment of the treating oncologist
* Enrolled in a clinical trial for AET
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Coping with AET side effects as measured by the Management of Current Stress - Part A (MOCS-A) questionnaire.