The Effect of Pre-Cesarean Section Guided Imagery

Menekşe Nazlı AKER

Status: Completed

Conditions: Cesarean Section

Treatments: Other: Guided imagery

Study type: Interventional

Funder types: Other

Identifiers

NCT05790954

15149

Details and patient eligibility

About

The aim of this study is to evaluate the effect of guided imagery applied before cesarean section on preoperative anxiety, fear and physiological parameters.

The study will be carried out in two different groups. The practice will start with meeting the women 3 days before cesarean section. 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 random. The following applications will be made to the groups.

Enrollment: 60 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• planned cesarean section
• Single birth
• giving birth at term
• No hearing problems
• Agreeing to participate in the research and obtaining written permission,

Exclusion criteria

• Emergency cesarean section due to a health problem of the mother or baby
• Not completing the study

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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60 participants in 2 patient groups

Guided imagery Group

Experimental group

Treatment:

Other: Guided imagery

Control Group

No Intervention group