Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05561270

Light Exposure on Pain in Hypermobile Ehlers-Danlos Syndrome

Led by New York Institute of Technology · Updated on 2024-05-06

30

Participants Needed

1

Research Sites

153 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic pain is a major complaint among many individuals living with hypermobile Ehlers Danlos Syndrome (hEDS) and may have a severe impact on quality of life and activities of daily living. Given the complexity of the disease's pathophysiology, effective treatments are limited. This investigation will examine the impacts of green light exposure on subject-reported pain severity and symptoms. Knowing whether this intervention can improve pain and quality of life in this population may offer valuable guidance to clinicians who treat hEDS patients and to hEDS patients themselves.

CONDITIONS

Official Title

Light Exposure on Pain in Hypermobile Ehlers-Danlos Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older and able to speak, read, and understand English
  • Diagnosed with hypermobile Ehlers-Danlos Syndrome (hEDS)
  • Average numeric pain score of 5 out of 10 or greater over the 10 weeks prior to enrolling and failure of medical therapy to control the pain
Not Eligible

You will not qualify if you...

  • Initiation of any new analgesic therapy within 30 days of enrollment (chronic therapy with stable regimen maintained for at least 30 days prior permitted)
  • Serious mental illness causing loss of contact with reality or Major Depression Disorder
  • History of color blindness or uncorrected cataracts
  • Receiving remuneration or have pending litigation for their medical conditions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

New York Institute of Technology College of Osteopathic Medicine

Old Westbury, New York, United States, 11568

Actively Recruiting

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Research Team

P

Philip Noto, DO

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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