Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
Healthy Volunteers
NCT07329309

Post-Caesarean Pranayama and Pain

Led by KTO Karatay University · Updated on 2026-02-09

100

Participants Needed

1

Research Sites

9 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effect of pranayama breathing exercises on postoperative pain and postpartum comfort levels in women following caesarean section, with the objective of providing important evidence for the integration of non-pharmacological methods into postpartum care.

CONDITIONS

Official Title

Post-Caesarean Pranayama and Pain

Who Can Participate

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Undergone a caesarean section under spinal anaesthesia
  • Reported a post-operative pain level of at least 4 on the Numerical Rating Scale (NRS)
  • Knowledge of Turkish
  • Ability to communicate effectively with the research team
  • Volunteer to participate in the study and provide written consent
Not Eligible

You will not qualify if you...

  • Having given birth by emergency caesarean section
  • Presence of pregnancy complications (e.g. pre-eclampsia, gestational diabetes, placenta praevia)
  • History of chronic pain or analgesic dependence
  • Requirement for admission to the intensive care unit in the early postoperative period
  • Need for additional surgical intervention
  • Development of significant intraoperative or postoperative complications
  • Refusal to exercise or intolerance to exercise
  • Failure to comply with study procedures
  • Withdrawal of consent
  • Incomplete follow-up
  • Development of a new medical condition during the study that could affect the results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Kto Karatay University

Konya, Turkey (Türkiye)

Actively Recruiting

Loading map...

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here