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MBSR Effects on Aging Anxiety and Body Image

K

KTO Karatay University

Status

Begins enrollment this month

Conditions

Middle Aged
Mindfulness Based Stress Reduction
Body Image

Treatments

Behavioral: bilinçli farkındalık temelli stres azaltma programı

Study type

Interventional

Funder types

Other

Identifiers

NCT07344896
Karatay University

Details and patient eligibility

About

This study was designed to determine the effect of a mindfulness-based stress reduction (MBSR) program on aging anxiety and body image among middle-aged women. The primary hypotheses to be tested are as follows:

H0a: There is no difference in the mean scores of the Aging Anxiety Scale between the women in the experimental group who receive the mindfulness-based stress reduction program and the women in the control group.

H0b: There is no difference in the mean scores of the Body Image Scale between the women in the experimental group who receive the mindfulness-based stress reduction program and the women in the control group.

H0c: There is no difference between the pre-intervention and post-intervention mean scores of the Aging Anxiety Scale among the women in the experimental group who receive the mindfulness-based stress reduction program.

H0d: There is no difference between the pre-intervention and post-intervention mean scores of the Body Image Scale among the women in the experimental group who receive the mindfulness-based stress reduction program.

The researchers will compare the experimental group with the control group in order to assess the effect of the mindfulness-based stress reduction program on aging anxiety and body image among middle-aged women.

Participants:

  • They will attend an 8-session mindfulness-based stress reduction program.
  • They will participate in one silent mindfulness retreat session.

Enrollment

58 estimated patients

Sex

Female

Ages

45 to 59 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • At least primary school graduate,
  • Being between 45-59 years old,
  • Living in Çumra district center,
  • Being open to communication and cooperation

Exclusion criteria

  • Those with chronic illnesses (self-report)
  • Foreign nationals Those with psychiatric illnesses (self-report) Those with physical disabilities and limited mobility

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

58 participants in 2 patient groups

mindfulness-based stress reduction program intervention group
Experimental group
Description:
After the pre-test, a mindfulness-based stress reduction program will be implemented. It will be evaluated with a post-test.
Treatment:
Behavioral: bilinçli farkındalık temelli stres azaltma programı
control group
No Intervention group
Description:
A pre-test will be administered. No practice will be conducted. Students will be evaluated with a post-test

Trial contacts and locations

0

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Central trial contact

Necibe ş tunalı, master

Data sourced from clinicaltrials.gov

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