Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:12 PM
Ignite Modification Date:
2025-12-24 @ 7:12 PM
NCT ID:
NCT02328703
Eligibility Criteria:
Inclusion Criteria:
* Be Active, Reserve, or National Guard with previous deployment(s) to OIF, OEF, or OND
* Be age 18 years or older
* Have ability to read and understand consent forms and study documents
* Have sustained at least one traumatic combat extremity injury defined as: single or both arm or leg, above or below knee amputation, mangled limb(s)
* Report, from a major traumatic extremity injury, an average and worst pain level ≥ 5 (numeric rating scale of 0 to 10) for at least one of three days prior to enrollment
* Be receiving a stable pain medication regimen defined as a regimen that may include multimodal analgesia with opioids, anticonvulsants and/or antidepressants for neuropathic pain in relatively stable doses with no more than a 10 to 20% increase over the past week prior to enrollment
* Have a cognitive performance evaluation that is consistent with an understanding of the proposed study as assessed by a "teach back" process
* Be receiving a minimum of two hours of physical therapy per day
Exclusion Criteria:
* Moderate to severe traumatic brain injury (TBI) as documented on the standardized evaluation completed by TBI Service providers
* Active moderate to severe psychological distress or psychiatric condition such as active psychosis, suicidal or homicidal ideation as documented, on the standardized psychological evaluation completed by a behavioral health psychiatrist
* Pregnancy
* Any medical condition that in the opinion of the participant's health care provider or PI has the potential to interfere with the effects of Reiki treatments
* Being pre-scheduled for additional surgeries or major painful and activity limiting procedures during the participant's participation in the study
* Received Reiki therapy treatment within the last three months.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02328703
Study Brief:
Protocol Section:
NCT02328703