the Effect of Reiki Application on Depression, Anxiety and Physical Activity in Patient With Multiple Sclerosis

Sponsor
Ataturk University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06129019
Collaborator
(none)
60
1
2
6.5
9.2

Study Details

Study Description

Brief Summary

During Reiki application, individuals may report feeling a slight warm sensation under and near the therapist's hand. The only rule in Reiki practice is that the individual must give permission to the practitioner to facilitate the flow of energy. The person receiving Reiki during the application does not have to believe in Reiki. Because Reiki is universal life energy and is available to everyone. Reiki is generally safe and no serious side effects have been reported. Reiki practice in the last 10 years; It is increasing among physicians, nurses and other healthcare professionals.

This study was planned to investigate the effect of reiki application on depression, anxiety and physical activity in individuals diagnosed with Relapsing-Remitting Multiple Sclerosis.

Geri bildirim gönder Yan paneller

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Reiki
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
Investigation of the Effect of Reiki Application on Depression, Anxiety and Physical Activity in Individuals Diagnosed With Relapsing-Remitting Multiple Sclerosis
Anticipated Study Start Date :
Nov 15, 2023
Anticipated Primary Completion Date :
Mar 20, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental:

Reiki application will be done

Behavioral: Reiki
Reiki application will be done

No Intervention: Control

Reiki application will not be done

Outcome Measures

Primary Outcome Measures

  1. Beck Depression Scale [4 week]

    The scale was administered to investigate each participant's feelings and attitudes regarding the general depressive state. Each patient was asked to read several groups of statements and then mark the one statement in each group that best described how he or she felt "during the past week." BDI, which evaluates four statements describing increasing intensities of depressive symptoms between 0 and 3 points, includes 21 items. Depressive symptoms were classified as follows: minimal-to-moderate depressive symptoms (range 14 to 19), moderate-to-severe depressive symptoms (range 20 to 29), severe depressive symptoms (range 30 to 63).

  2. Beck Anxiety Scale [4 week]

    BAI is a self-rating scale developed by Beck et al. (1988) and used to determine the frequency of anxiety symptoms experienced by individuals. It is a Likert-type scale consisting of 21 items and scored between 0-3. Its validity and reliability in Turkey were determined by Ulusoy et al.

  3. International Physical Activity Survey [4 week]

    There are some scales that can be used in primary care to evaluate physical mobility. One of these is the "International Physical Activity Questionnaire", which was developed by the International Consensus Group consisting of researchers from various countries with the support of the World Health Organization and the Center for Disease Control, to be used to measure physical activity and inactivity in 1997 and 1998; (IPAQ)" is a standard tool. Reliability and/or validity studies were conducted in 14 centers from 12 countries in 2000 for at least two of the four long (IPAQ-long) and four short (IPAQ-SF) forms of the IPAQ. This scale was adapted into Turkish as long form (UF) and short form (SF) under the name "International Physical Activity Questionnaire (UFAA)" and its validity and reliability study was conducted by Sağlam et al. in 2010

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being over 18 years of age

  • Having the ability to use technological devices

  • Not using Reiki and similar integrative treatment methods

  • No verbal communication disability (hearing and speaking)

  • Not having a diagnosed psychiatric disorder

  • Patients who have been receiving Relapsing-Remitting MS treatment for more than three months

Exclusion Criteria:
  • Patients using any complementary alternative treatment methods

  • Patients who cannot communicate by phone to participate in remote reiki application

  • Patients with autoimmune diseases other than multiple sclerosis

  • Patients with communication disabilities

  • Patients with another known neurological system disease (dementia, Alzheimer's, etc.).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Firat University Elazıg Turkey

Sponsors and Collaborators

  • Ataturk University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
gülcan bahcecioğlu, Principal Investigator, Ataturk University
ClinicalTrials.gov Identifier:
NCT06129019
Other Study ID Numbers:
  • 22/11
First Posted:
Nov 13, 2023
Last Update Posted:
Nov 13, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by gülcan bahcecioğlu, Principal Investigator, Ataturk University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 13, 2023