Ireland
--:--IST
Recruiting Not applicable

Effect of Reiki on Neuropathic Pain Severity and Sleep Quality in Patients With Diabetic Neuropathy

NCT06668623 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-11-01
Last updated
2025-02-14

Condition(s) studied

Diabetic Neuropathy

Investigational drug(s) / intervention(s)

Reiki GroupSham Reiki Group

Reiki Group: Remote Reiki application will be performed once a day for 20 minutes for four days by a researcher who has received second level training. No changes will be made to the standard treatment plan of the patients during the application.

Sham Reiki Group: In the placebo group, the Sham Reiki group will receive remote Reiki application in accordance with the application protocol by a nurse who is not a Reiki practitioner trained by the researcher and has not received any previous training.

Study summary

The study is planned to be conducted in a mixed research design with quantitative and qualitative types. The quantitative phase of the study was planned as a single-blind, randomized controlled study with Reiki group, Sham Reiki group and control group designs in order to examine the effect of second-level (remote application) Reiki applied to patients with diabetic neuropathy for 20 minutes a day for four days on pain intensity, neuropathic pain intensity (DN4 Questionnaire) total scores and sleep quality. The qualitative study will be conducted with 4 people from the Reiki and Sham Reiki groups, a total of 8 patients, one week after the application, using the individual in-depth interview method and a semi-structured questionnaire.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Over 18 years of age * No communication problems * Communicating in Turkish * No diagnosis of mental illness * Willingness to participate in the study * Being competent enough to answer forms and surveys * VAS pain intensity 3 and above * 4 Question Neuropathic Pain score 4 and above * Not having received Reiki treatment Exclusion Criteria: * Receiving a different illness and treatment during the therapy process * Leaving Reiki practice * Psychiatric illness * Becoming a Reiki practitioner or instructor * Cerebrovascular disease * Receiving Reiki practice

Primary outcome measure(s)

  • Visual Analog Scale(VAS) — Pre-test data will be collected before starting the study and post-test data will be collected 1 week later.
    The value of "0 points" in the scale, which indicates the absence of pain, indicates a good condition, and the maximum value, "10 points", indicates a bad condition with unbearable pain intensity.

Trial sites (1)

FacilityCityRegionStatus
Kayseri City Hospital Kayseri Kocasinan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06668623 on ClinicalTrials.gov ↗ ← All trials in Turkey