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Not Yet RecruitingNCT06870214

Benson Relaxation Technique and Stress in Pregnancy

''Investigation of the Effect of Benson Relaxation Technique Applied to Pregnant Women on Fear of Childbirth, Anxiety and Stress Levels of Pregnant Women''

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Ondokuz Mayıs University · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to determine the effect of the Benson Relaxation Technique applied to pregnant women on their fear of birth, anxiety and stress levels.

Detailed description

The aim of this study is to determine the effect of the Benson Relaxation Technique applied to pregnant women on their fear of birth, anxiety and stress levels. Hypotheses ; H0-1: Benson relaxation technique applied to pregnant women has an effect on childbirth. H1-1: Benson relaxation technique applied to pregnant women has no effect on childbirth. H0-2: Benson relaxation technique applied to pregnant women has no effect on anxiety. H1-2: Benson relaxation technique applied to pregnant women has an effect on anxiety. H0-3: Benson relaxation technique applied to pregnant women and their partners has no effect on stress. H1-3: Benson relaxation technique applied to pregnant women and their partners has an effect on stress The study will be conducted on two different groups. The application will be a 1-hour Benson relaxation technique applied to pregnant women in the third trimester every week for 4 weeks. Participants will be asked to do relaxation exercises twice a day, morning and evening, for 10 to 15 minutes for 1 month. A phone number that patients can call with questions will also be provided. In addition, the researcher will call the women in the intervention group every week to follow up on the relaxation process and answer questions. After the women are evaluated in terms of eligibility criteria for the study, information about the study will be provided to the women who are eligible and written informed consent will be obtained from the women who accept. The random distribution of the women to the study groups will be carried out using the Block Randomization method. The following applications will be applied to the groups. The researcher will contact the experimental group by phone. The application will end after 4 weeks.

Conditions

Interventions

TypeNameDescription
OTHERrelaxationWomen in the 3rd trimester will receive routine care only.

Timeline

Start date
2025-06-15
Primary completion
2025-10-15
Completion
2025-10-30
First posted
2025-03-11
Last updated
2025-04-02

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06870214. Inclusion in this directory is not an endorsement.