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Search / Trial NCT07090902

The Effect of Progressive Relaxation Exercise

Launched by KARABUK UNIVERSITY · Jul 24, 2025

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Progressive Relaxation Exercise Labor Pain Delivery Method Breastfeeding

ClinConnect Summary

This clinical trial is studying whether a special childbirth preparation program that includes relaxation exercises can help pregnant women feel more comfortable during labor, influence their choice of delivery method, and improve their early breastfeeding experience. The program provides participants with an educational booklet, an audio CD guiding them through relaxation exercises, and face-to-face training sessions. Women in the study who do not receive this program will continue with their usual prenatal care. The goal is to see if learning these relaxation techniques can make labor less painful and support women in their decisions and postpartum comfort.

Women who are pregnant, between 18 and 49 years old, and able to attend the training sessions regularly may be eligible to join. Participants must not have any pregnancy or health complications and should be willing to take part fully in the study. Those who have certain medical conditions, have practiced similar relaxation techniques before, or are taking certain medications won’t be eligible. If accepted, participants will be guided through the relaxation exercises and monitored throughout their pregnancy to understand how this approach might help with labor pain and breastfeeding comfort.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female participants aged between 18 and 49 years
  • Currently pregnant
  • Willing to participate in the study and provide informed consent
  • Able to attend the planned training sessions regularly
  • No complications during pregnancy, childbirth, or postpartum for themselves or their newborn
  • Exclusion Criteria:
  • Not within the age range of 18-49
  • Not currently pregnant
  • Fails to complete study questionnaires or withdraws from the study
  • Has communication difficulties or cognitive impairment
  • Fails to attend training sessions regularly
  • Has open wounds or allergic skin conditions
  • Develops postpartum complications (e.g., bleeding, infection, fever)
  • Has cardiac arrhythmia or uses a pacemaker
  • Diagnosed with conditions such as epilepsy or pre-eclampsia
  • Has kidney or liver disease
  • Previously practiced progressive muscle relaxation techniques
  • Is morbidly obese (BMI \> 40)
  • Uses chronic opioids, antidepressants, or psychoactive medications

About Karabuk University

Karabuk University is a distinguished educational institution located in Turkey, dedicated to advancing scientific research and innovation across various fields, including healthcare. As a clinical trial sponsor, the university plays a pivotal role in facilitating cutting-edge research aimed at improving patient outcomes and contributing to the global body of medical knowledge. With a commitment to ethical standards and rigorous scientific methodology, Karabuk University collaborates with healthcare professionals and researchers to design and implement clinical trials that address pressing health challenges, ultimately striving to enhance treatment options and promote public health initiatives.

Locations

Samsun, , Turkey

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported