Actively Recruiting

Phase Not Applicable
Age: 5Years +
All Genders
NCT07019259

Light Therapy for Chemotherapy Induced Peripheral Neuropathy in Childhood Cancer Survivors

Led by Yale University · Updated on 2025-07-14

20

Participants Needed

2

Research Sites

61 weeks

Total Duration

On this page

Sponsors

Y

Yale University

Lead Sponsor

R

Rally Foundation for Childhood Cancer Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Light Therapy for Chemotherapy Induced Peripheral Neuropathy in Childhood Cancer Survivors

Who Can Participate

Age: 5Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • History of childhood cancer (diagnosed before 21 years of age)
  • Current age 5 years or older
  • History of exposure to vinca alkaloid, platinum, or other chemotherapy that can cause CIPN
  • Presence of CIPN with a neuropathy score of 4 or higher on appropriate assessment depending on age
Not Eligible

You will not qualify if you...

  • Currently pregnant or lactating
  • Unable to sit still for at least 15 minutes
  • Neuropathy diagnosis before cancer treatment
  • Active cancer diagnosis or cancerous skin lesion
  • Central nervous system tumor
  • Cancer lesion or open wound in the treatment area or any condition worsened by device use

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Yale New Haven Health Smilow York Street Hospital

New Haven, Connecticut, United States, 06520

Actively Recruiting

2

Yale New Haven Health Park Avenue Medical Center

Trumbull, Connecticut, United States, 06611

Actively Recruiting

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Research Team

R

Rozalyn Rodwin, MD

CONTACT

J

Jaime Rotatori, BSN, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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