Acupressure for Pain and Opioid Use Among Breast Cancer Patients
Stopped early · Not applicable
Conditions studied: Breast Cancer, Fatigue, Chronic Pain
In brief
This study seeks to determine the feasibility of recruiting and training participants in self-acupressure, for women undergoing primary breast cancer surgery or delayed reconstruction surgery. The study seeks to determine also if self-acupressure is effective in reducing the need for opioids post-surgery and the effects on other life factors.
Key facts
- Study ID
- NCT03655600
- Run by
- University of Michigan
- People needed
- 8
- Starts
- 2018-09-17
- Expected to finish
- 2019-10-17
- Last updated by the study team
- 2019-10-25
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of breast cancer stage 0 to III;
- Planned unilateral or bilateral mastectomy or planned delayed breast reconstruction surgery within 24 months following unilateral or bilateral mastectomy;
- For delayed breast reconstruction patients only: apparently cancer free at time of delayed reconstruction;
- No planned new interventions for pain the two weeks prior to surgery;
- Able to self-administer treatment at the specified points.
You may not qualify if…
- Medically unstable (e.g. uncontrolled diabetes, high blood pressure, etc.);
- For delayed breast reconstruction only: taking aromatase inhibitors which could confound surgical and chronic pain measurements;
- Have a diagnosis of untreated mood disorder, e.g., bipolar or major depressive disorder;
- Unwilling to maintain stable does of allowed chronic pain medications (e.g. NSAIDS, benzodiazepines, SSRIs and SNRIs);
- Pregnant, those planning a pregnancy, or lactating mothers;
- Any medical condition or treatment factor that the study team feels would either compromise the data acquired or introduce a potential safety concern.
- Unable to give consent;
- Acupuncture or acupressure receipt in past year
Where it is running
- Chronic Pain and Fatigue Research Center, University of Michigan — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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