Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
120 participants
INTERVENTIONAL
2024-06-30
2024-11-10
Brief Summary
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Detailed Description
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The study will be carried out in three different groups. The practice will start with meeting the women whose children were treated in the hospital. After the women are evaluated in terms of eligibility criteria for the research, the women who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.
Reiki Group The intervention will be applied to the reiki group to be applied in the hospital room. Reiki therapy will be applied by a practitioner with a Reiki application certificate in the application laboratory for 30 minutes while the participants lie down with their eyes closed. 4 sessions of reiki application will be applied to the intervention group for a week. Anxiety level after 4 sessions will be recorded.
Placebo Reiki will be applied to the participants in the group in the application hospital room. The practice will be carried out in the application laboratory for 30 minutes, with the participants sitting with their eyes closed. Reiki life energy will not be transferred to participants in the placebo reiki group. Since the participants' eyes are closed, they will not know that there is a transfer. Placebo Reiki application will be performed in the room 4 times during a week. Placebo application will start, and the first anxiety scores will be recorded. After 4 sessions, anxiety scores will be recorded.
control group; the first anxiety scores will be recorded. After a week later anxiety scores will be recorded.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Reiki
The intervention will be applied to the reiki group in the application hospital room. Reiki therapy will be applied by a practitioner with a Reiki application certificate in the application laboratory for 30 minutes while the participants lie down with their eyes closed. 4 sessions of reiki application will be applied to the intervention group for a week. Reiki application will start , the first anxiety scores will be recorded. Anxiety levels after 4 sessions will be recorded.
reiki
reiki
Placebo reiki
Placebo Reiki will be applied to the participants in the group in the application hospital room. The practice will be carried out in the application room for 30 minutes, with the participants sitting with their eyes closed. Reiki life energy will not be transferred to participants in the placebo reiki group. Since the participants' eyes are closed, they will not know that there is a transfer. Placebo Reiki application will be performed in the room 4 times during a week. Placebo application will start and the anxiety scores will be recorded. After 4 sessions, anxiety scores will be recorded.
placebo reiki
placebo reiki
control
Routine hospital procedure will be applied. Anxiety scores will be recorded. After a week anxiety scores will be recorded.
No interventions assigned to this group
Interventions
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reiki
reiki
placebo reiki
placebo reiki
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Their child has an acute or chronic disease
* Able to speak and write Turkish and have no communication problems
* No psychiatric history and not using medication
* Not drinking alcohol in the last 24 hours
* Those who have not received body-mind therapy (yoga, reiki, massage, meditation) in the last six months
* Mothers who volunteer to participate in the research will be included.
Exclusion Criteria
* Having time and communication problems that cannot answer the questions asked
* Mothers who do not volunteer to participate in the study will not be included in the study.
18 Years
60 Years
FEMALE
Yes
Sponsors
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Ondokuz Mayıs University
OTHER
Responsible Party
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Sümeyye BAL
Director
Principal Investigators
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Sümeyye BAL, Ph.D.
Role: STUDY_DIRECTOR
Ondokuz Mayıs University
Locations
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Ondokuz Mayis University
Samsun, , Turkey (Türkiye)
Countries
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Other Identifiers
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2022/292
Identifier Type: -
Identifier Source: org_study_id
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