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Light Therapy for Chemotherapy Induced Peripheral Neuropathy in Childhood Cancer Survivors
Sponsor: Yale University
Summary
The purpose of this study is to determine feasibility and acceptability of a six-week at-home light therapy protocol in childhood cancer survivors, to identify facilitators and barriers to implementing this intervention, and to measure signs and symptoms of Chemotherapy Induced Peripheral Neuropathy (CIPN) at baseline and following completion of the at-home light therapy protocol.
Key Details
Gender
All
Age Range
5 Years - Any
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2025-06-30
Completion Date
2026-09
Last Updated
2025-07-14
Healthy Volunteers
No
Interventions
Anodyne Therapy System
Survivors will be provided the Anodyne Therapy System Model 120 to use as part of a 6-week at-home light therapy intervention. Participants will be instructed on where apply the device based on location of their symptoms, and will be instructed to use the device for 15 minutes per day, 3 days per week. Proper use of the device will be demonstrated in clinic by a trained physical therapist or study team member.
Locations (2)
Yale New Haven Health Smilow York Street Hospital
New Haven, Connecticut, United States
Yale New Haven Health Park Avenue Medical Center
Trumbull, Connecticut, United States