Assessment of Cancer Concerns at the End of Treatment (ACE)
Completed
Conditions studied: Breast Cancer(BC) Survivors
In brief
This study will describe patient-reported symptom burden and concerns, quality of life (QOL), and health behaviors of breast cancer(BC) survivors who have completed initial treatments (e.g., surgery, chemotherapy, and/or radiotherapy), assess the feasibility of using a web-based platform to collect patient-reported outcome (PRO) data, and evaluate provider satisfaction following delivery of an electronic health record (HER)/EPIC summary of these PROs. Secondary aims will estimate differences in referral to available services between those providers exposed to the PRO summary and historical controls. BC survivors who have completed initial treatment and present within the first year following treatment for an end of treatment (EOT)/survivorship focused visit will be the focus of this study.
Key facts
- Study ID
- NCT02514486
- Run by
- Abramson Cancer Center at Penn Medicine
- People needed
- 332
- Starts
- 2014-07-01
- Expected to finish
- 2018-01-19
- Last updated by the study team
- 2020-04-03
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with invasive, non-metastatic BC (Stage I, II, or III) without hematogenous or distant metastases
- Have completed initial treatment (chemotherapy, radiotherapy, and/or surgery). May still be receiving hormonal or targeted therapy (e.g., tamoxifen, aromatase inhibitors).
- Within 1 year of completing primary treatment
- Scheduled for an EOT visit
- Age 18 years or older
- Can understand written English
- Have internet access and a working email address
You may not qualify if…
- Diagnosed with non-invasive (Stage 0/DCIS) or metastatic (Stage IV) cancer or hematogenous or distant metastatic disease
- No working email address -
Where it is running
- Abramson Cancer Center of the University of Pennsylvania — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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