The Effect of Reiki Applicatıon on Sleep and Qualıty of Life in Epılepsy Patıents

June 7, 2023 updated by: gülcan bahcecioğlu, Ataturk University

After the general period of positive social adjustments, epilepsy is in a high life cycle to control seizures. During seizures in epilepsy, patients' quality of life and antiepileptic life span can be seen in daily life such as daily life and daily awakenings.

Reiki, which has been proven by studies in health problems such as fatigue and pain; an energy that can be unblocked or applied in a non-applicable way can benefit from a therapy that can be applied by touch or remotely, without negative effects. In the literature, reiki applied to epilepsy patients has sleep and quality of life. This thesis is planned to do research on sleep and living areas of reiki applied to epilepsy patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This research; It will be carried out on a voluntary basis with the treatment of 60 patients with epilepsy, 30 of which will be tested, 30 of which will be comprehensive, from the University of Fır Hospital Neurology Clinic Polyclinic and those over 18 years of age, who can communicate adequately, who have psychiatric problems, who are in the last six body mind, who can control the phone, who will come to the scale, who will come to sleep. The study will be a pretest-posttest controlled group study. Data; Patient Information Form will be collected with Pittsburgh Sleep Quality Scale, Quality of Life in Epilepsy Scale. The control method will not interfere. If we try, first the application places and the way of doing it will be shown. Administration through 4 weeks, first consecutive week; 1 session face-to-face 30-45 minutes, then 3 sessions of 21 minutes of training, 2 sessions of 21 minutes of training in the other 3 training courses, a total of 4 weeks 10. For face-to-face reiki; A room will be used inside the hospital. Reiki to 7 different chakras to be taken in the first session. For the other sessions, before the application, all will be called and informed about the reiki will be sent, and then he will apply reiki from a distance for 21 minutes by using the training and reiki symbols. The scales will be reapplied by the researcher, either face to face or face to face, during the experiment and 4 weekends to be controlled. Finally, there will be a significant difference between the pretest and the son test.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Merkez
      • Elazığ, Merkez, Turkey, 23100
        • Gülcan B Turan

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.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

  • be over 18 years old
  • Ability to communicate adequately
  • Absence of psychiatric problems
  • Not having received body-mind therapy (yoga, reiki, massage, meditation) in the last six months
  • Volunteering to participate in the research
  • Own a phone
  • Having a scale score of greater than 5 according to the Pittsburgh Sleep Quality Scale
  • Not using sleeping pills 4.4.2. Exclusion Criteria from Research
  • being under the age of 18
  • Having trouble communicating
  • Having a psychiatric problem
  • Having received body-mind therapy (yoga, reiki, massage, meditation) in the last six months
  • Not being willing to participate in the research
  • Not having a phone
  • Having a scale score of less than and/or equal to 5 on the Pittsburgh Sleep Quality Scale
  • Using sleeping pills

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental:
reiki will be aplicated
reiki
Other Names:
  • life quality
No Intervention: Control
Routine maintenance will be applied.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pittsburgh Sleep Quality Index
Time Frame: 1 hours later
The Pitssburgh sleep quality index, developed by Buysse et al. in 1989, is used to evaluate the quality of sleep, the amount of sleep, the presence and severity of sleep disorders in the last month. Agargun et al. They adapted PUKI to Turkish in 1996.There are seven components in the scale. These; subjective sleep quality (component 1), sleep latency (component 2), sleep duration (component 3), habitual sleep efficiency (component 4), sleep disturbance (component 5), use of sleeping pills (component 6) and daytime dysfunction (component 3) 7) stop. The evaluation score of each item is between 0-3, and the total score obtained at the end of the evaluation is between 0-21. A total score of 5 and less than 5 defines good sleep, and a total score of more than 5 defines poor sleep
1 hours later
Quality of Life Scale in Epilepsy
Time Frame: 1 hours later
The Quality of Life Scale for Patients with Epilepsy was developed by Vickrey et al. in 1993. Mollaoğlu et al. carried out the validity and reliability studies of this scale in Turkey in 2015. The scale includes 7 sub-dimensions. These sub-dimensions are; anxiety about seizures (5 items), effects of drugs (3 items), energy/fatigue (4 items), emotional well-being (5 items), cognitive function (6 items), social function (5 items), total quality of life (2 items) ) and an additional item that evaluates the total health status, a total of 31 items. Scale scoring is in the range of 0-100. High score indicates higher quality of life
1 hours later

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 15, 2022

Primary Completion (Actual)

February 25, 2023

Study Completion (Actual)

May 1, 2023

Study Registration Dates

First Submitted

November 23, 2022

First Submitted That Met QC Criteria

December 1, 2022

First Posted (Actual)

December 2, 2022

Study Record Updates

Last Update Posted (Actual)

June 8, 2023

Last Update Submitted That Met QC Criteria

June 7, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2022/30-34

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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