The Effect of Reiki on Cesarean During Hospitalization

The Effect of Reiki Applied to Women Who Have Been Hospitalized by Cesarean During the Hospitalization Process on Anxiety, Depression, Comfort and Breastfeeding

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06437769

Enrollment

Registered

2024-05-31

Start date

2024-06-03

Completion date

2025-03-03

Last updated

2025-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Section Complications

Brief summary

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

Detailed description

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

Interventions

OTHERreiki

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

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

SINGLE (Subject)

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 60 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
anxiety and depression	immediately after intervention	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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026