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Benson Relaxation Technique and Stress in Pregnancy

O

Ondokuz Mayıs University

Status

Not yet enrolling

Conditions

Relation, Interpersonal
Anxiety
Stress

Treatments

Other: relaxation

Study type

Interventional

Funder types

Other

Identifiers

NCT06870214
2024-930

Details and patient eligibility

About

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.

Full 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.

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

relaxation group
Experimental group
Description:
They will be interviewed according to the inclusion criteria and exclusion criteria, and they will be informed about the study and their consent will be obtained, the participant information form and depression form will be filled, a pre-test will be performed and the communication will be completed. Their numbers will be taken. The intervention group will be given a 1-hour Benson relaxation technique every week for 4 weeks. Participants will be asked to do relaxation exercises for 10 to 15 minutes twice a day, in the morning and evening, for 1 month. A phone number will be provided for patients to call if they have questions. In addition, the researcher will call the women in the intervention group every week to follow up on the relaxation process and answer questions. The researcher will contact the experimental group by phone. He/she will introduce himself/herself and final tests will be conducted after 4 weeks.
Treatment:
Other: relaxation
control group
No Intervention group
Description:
\*\*"Routine nursing care will be provided."\*\*

Trial contacts and locations

1

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Central trial contact

Sümeyye BAL, Ph.D

Data sourced from clinicaltrials.gov

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