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Clinical Outcomes and Patient Satisfaction With Use of the Amma System
Sponsor: Providence Health & Services
Summary
The primary goal is to conduct a pilot evaluation of the Amma device, to determine whether it is feasible to offer as an option for patients within oncology suites within the PH\&S system.
Official title: Observational Study of Clinical Outcomes and Patient Satisfaction With Use of the Amma System
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
15
Start Date
2022-08-22
Completion Date
2025-12
Last Updated
2025-03-10
Healthy Volunteers
No
Conditions
Interventions
Amma Cooling Caps
Once enrolled, subjects will be provided the Amma device by the clinic on days of chemotherapy treatment, and upon completion of treatment it will be returned to the clinic for safekeeping. Upon completion of chemotherapy, anywhere from 3-6 weeks following treatment, subjects will repeat the questionnaires and their hair will be photographed again. The overall duration of the study for subjects will be anywhere from 4 months to 8 months, depending on the duration of their chemotherapy regimen.
Locations (3)
Providence Cancer Institute - Newberg Clinic
Newberg, Oregon, United States
Providence Portland Medical Center
Portland, Oregon, United States
Providence Oncology and Hematology Care - Westside
Portland, Oregon, United States