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
70 participants
INTERVENTIONAL
2024-06-03
2025-03-03
Brief Summary
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Method: The study will be completed in a randomized controlled manner with a total of 70 women, 35 in the experimental group and 35 in the control group. Women in the experimental group Reiki therapy will be applied to the participants for 30 minutes while they lie down with their eyes closed. Research data will be collected with the Comfort Scale, Hospital anxiety and depression scale and bristol breastfeeding points and will be recorded
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Reiki
. Reiki therapy will be applied to the participants for 30 minutes while they lie down with their eyes closed. A total of 4 sessions of Reiki application will be applied to the intervention group at the 4th hour, 8th hour, 24th hour and 28th hour after the cesarean section. Reiki application will be applied at the 4th hour after the cesarean section. Comfort, anxiety, depression and breastfeeding symptoms after the 4th session will be recorded.
reiki
effect of reiki application to women who have been hospitalized by ceserean during the hospitlalization process on anxiety depression comfort and breastfeesing
control group
will provided with standard midwifery care.
No interventions assigned to this group
Interventions
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reiki
effect of reiki application to women who have been hospitalized by ceserean during the hospitlalization process on anxiety depression comfort and breastfeesing
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* be over 18 years old
* Not having a diagnosed psychiatric disease
* no communication problems
* No drug sensitivity or allergy
* women who have had a cesarean section
Exclusion Criteria
* no communication problems
* Being under 18 years of age
* not volunteering to participate in the research
* drug sensitivity and allergy
* women who gave birth normally
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: PRINCIPAL_INVESTIGATOR
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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2024/236
Identifier Type: -
Identifier Source: org_study_id
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