The Effect of Reiki on Cesarean During Hospitalization

Ondokuz Mayıs University70 enrolled

Overview

To determine the effect of reiki applied to women who have been hospitalized by cesarean during the hospitalization process on anxiety, depression, comfort and breastfeeding 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

Design and Settings: This randomized controlled experimental study will conducted in the post operative room of the, Turkey between the dates of June 2024 and October 2024

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

SINGLE

Enrollment

Conditions

Cesarean Section Complications

Interventions

reikiOTHER

effect of reiki application to women who have been hospitalized by ceserean during the hospitlalization process on anxiety depression comfort and breastfeesing

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * volunteering * 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: * Having a diagnosed psychiatric illness * 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

Locations (1)

Ondokuz Mayis University

Samsun, Turkey (Türkiye)

Outcomes

Primary Outcomes

anxiety and depression

Hospital Anxiety and Depression Scale;Hospital anxiety depression scale, to screen anxiety and depression in people with physical illnesses. has been prepared. It consists of 14 items.

Time frame: immediately after intervention

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.