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Completed

NCT Number: NCT06870214

Benson Relaxation Technique and Stress in Pregnancy

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.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Ondokuz Mayis University

Samsun, 55200, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Those who are in their 28th-38th weeks of pregnancy,
  • People with mental illness,
  • People who have Anxiety disorder,
  • People with hearing loss;
  • People who have no experience of using relaxation methods in the past,
  • People who have not used herbal or medical sedatives

Exclusion criteria

  • Those who do not want to participate in the intervention,
  • Those who have a termination of pregnancy during the intervention,
  • Those who have a risky pregnancy

Treatment and study plan

relaxation

Other

Women in the 3rd trimester will receive routine care only.

Other names: control group

Primary outcomes

  1. 1.Change in anxiety

    Time frame: immediately intervention 4 weeks later

    Beck Anxiety Inventory scale (BAI). The BAI measures only the frequency of anxiety symptoms in detail. It is a Likert-type self-assessment scale comprised of 21 items scored between 0 and 3. The higher the total score, the higher the anxiety experienced by the person (minimal: 0-7, mild: 8-15, moderate:16-25, and severe: 26-63 points). 18 The Turkish validity and reliability of the BSI has been reported by Ulusoy et al.

Sponsors and collaborators

Lead sponsor

Ondokuz Mayıs University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 11, 2025
Registry last updated
Jul 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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