Far Red Light to Improve Functioning in PAD

Description

The LIGHT PAD Trial is a Phase II multi-centered randomized clinical trial to collect preliminary data to test whether daily far red light treatment of the lower extremities in people with PAD improves six-minute walk distance, lower extremity perfusion, and ischemia-related damage in gastrocnemius muscle at four-month follow-up, compared to a sham control. Participants will complete 10 minutes of twice daily home treatment with either far red light or a sham light for four months.

Conditions

Peripheral Artery Disease, Peripheral Vascular Disease, Aging, Walking, Difficulty

Study Overview

Study Details

Study overview

The LIGHT PAD Trial is a Phase II multi-centered randomized clinical trial to collect preliminary data to test whether daily far red light treatment of the lower extremities in people with PAD improves six-minute walk distance, lower extremity perfusion, and ischemia-related damage in gastrocnemius muscle at four-month follow-up, compared to a sham control. Participants will complete 10 minutes of twice daily home treatment with either far red light or a sham light for four months.

Far Red Light to Improve Functioning in PAD: The LIGHT PAD Trial

Far Red Light to Improve Functioning in PAD

Condition
Peripheral Artery Disease
Intervention / Treatment

-

Contacts and Locations

Chicago

Northwestern University, Chicago, Illinois, United States, 60611

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Above- or below-knee amputation
  • 2. Critical limb ischemia defined as an ABI \<0.30 or \<0.40 with symptoms of rest pain
  • 3. Wheelchair confinement or requiring a walker to ambulate
  • 4. Walking is limited by a symptom other than PAD
  • 5. Current foot ulcer on bottom of foot
  • 6. Failure to successfully complete the study run-in
  • 7. Planned major surgery, coronary or leg revascularization during the next four months
  • 8. Major surgery, coronary or leg revascularization or major cardiovascular event in the previous three months
  • 9. Major medical illness including lung disease requiring oxygen, Parkinson's disease, a life-threatening illness with life expectancy less than six months, or cancer requiring treatment in the previous two years. \[NOTE: potential participants may still qualify if they have had treatment for an early stage cancer in the past two years and the prognosis is excellent, unless the cancer is located in the lower extremities. Participants who require oxygen only at night may still qualify.\]
  • 10. Mini-Mental Status Examination (MMSE) score \< 23
  • 11. Non-English speaking
  • 12. Participation in or completion of a clinical trial in the previous three months. \[NOTE: after completing a stem cell or gene therapy intervention, participants will become eligible after the final study follow-up visit of the stem cell or gene therapy study so long as at least six months have passed since the final intervention administration. After completing a supplement or drug therapy (other than stem cell or gene therapy), participants will be eligible after the final study follow-up visit as long as at least three months have passed since the final intervention of the trial.\]
  • 13. Visual impairment that limits walking ability.
  • 14. Six-minute walk distance of \<400 feet or \>1700 feet.
  • 15. Participation in a supervised treadmill exercise program or a cardiac rehabilitation program in previous three months or planning to begin a supervised treadmill exercise program or a cardiac rehabilitation program in the next five months.
  • 16. Unwilling to avoid red light therapy outside of study participation.
  • 17. Baseline blood pressure \<100/45.
  • 18. In addition to the above criteria, investigator discretion will be used to determine if the trial is unsafe or not a good fit for the potential participant.

Ages Eligible for Study

50 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Northwestern University,

Study Record Dates

2027-06-01