Pilot for The Breast Cancer Endocrine Therapy Adherence (BETA) Trial
Completed · Not applicable
Conditions studied: Breast Cancer
In brief
Pilot study to assess feasibility and patient acceptance of a text message cell phone application for patients with stage I-III, hormone receptor positive breast cancer who start adjuvant endocrine therapy.
Key facts
- Study ID
- NCT02256670
- Run by
- Yale University
- People needed
- 100
- Starts
- 2014-10-01
- Expected to finish
- 2016-08-01
- Last updated by the study team
- 2017-02-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with histologically confirmed stage I-III, estrogen and/or progesterone receptor positive, as defined by ASCO-CAP guidelines, invasive breast cancer for whom adjuvant hormonal therapy is indicated following standard NCCN practice guidelines
- Patients may enter the study before or within one month of starting endocrine treatment
- Patients with synchronous bilateral breast cancers are eligible if both tumors are hormone receptor positive
- Patient must be able to provide informed consent and agree to:
- Complete questionnaires according to the pre-specified study design
- Own a personal cell phone, agree to receive text messages on a monthly basis (including any costs), and share their personal cell phone number to receive text message reminder
- sign consent to allow research staff to contact their pharmacies to determine prescription refill dates
You may not qualify if…
- Patients with ductal carcinoma in situ
Where it is running
- Yale New Haven Hospital — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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