Clinical Trials Directory

Trials / Completed

CompletedNCT07384637

Effects of Progressive Relaxation Exercises and Planned Training After Cesarean Section on Pain, Anxiety and Comfort

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
129 (actual)
Sponsor
Cumhuriyet University · Academic / Other
Sex
Female
Age
19 Years – 35 Years
Healthy volunteers
Accepted

Summary

Effects of Progressive Relaxation Exercises and Planned Training after Cesarean Section on Pain, Anxiety and Comfort

Detailed description

The study consisted of a total of 129 women who underwent cesarean section (progressive relaxation exercise group: 43, planned training group: 43, control group: 43). Data were collected using a Personal Information Form, Visual Analog Scale, State-Trait Anxiety Inventory, and Postpartum Comfort Scale. Intergroup comparisons revealed statistically significant differences (p˂0.05) in the mean scores of the Visual Analog Scale, State Anxiety Inventory, Trait Anxiety Inventory, and Postpartum Comfort Scale in the post-test after exercise and training for women in the exercise, training, and control groups. After progressive relaxation exercise and training, pain levels decreased in women in the exercise and training groups, anxiety levels decreased in women in the training group, and comfort levels increased in women in both the exercise and training groups.

Conditions

Interventions

TypeNameDescription
BEHAVIORALProgressive Relaxation Exercise groupOn the first postoperative day, the women were met with, informed, and their written consent was obtained. Women in the Progressive Relaxation Exercise group who met the inclusion criteria were administered the Personal Information Form, Visual Analog Scale, State-Trait Anxiety Inventory, and Postpartum Comfort Scale via face-to-face interviews on the first postoperative day. Completing all forms took 15-20 minutes. Relaxation exercises began with breathing exercises, continued with muscle relaxation exercises, and lasted 30 minutes. In the final test phase, the Visual Analog Scale, State-Trait Anxiety Inventory, and Postpartum Comfort Scale were repeated on the second postoperative day.
BEHAVIORALPlanned Education groupOn the first postoperative day, the women were met with, informed, and their written consent was obtained. Women in the Planned Education group who met the inclusion criteria were administered the Personal Information Form, Visual Analog Scale, State-Trait Anxiety Inventory, and Postpartum Comfort Scale via face-to-face interviews on the first day. Completing all forms took 15-20 minutes. The training was conducted face-to-face by the researcher for each woman, in accordance with adult education principles, and lasted 30-45 minutes.

Timeline

Start date
2023-01-01
Primary completion
2023-12-30
Completion
2023-12-30
First posted
2026-02-03
Last updated
2026-02-17

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07384637. Inclusion in this directory is not an endorsement.