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RECRUITING
NCT07019259
NA

Light Therapy for Chemotherapy Induced Peripheral Neuropathy in Childhood Cancer Survivors

Sponsor: Yale University

View on ClinicalTrials.gov

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

DEVICE

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