ClinicalTrials.gg
Not yet recruitingNCT07344896Updated Aug 25, 2026

MBSR Effects on Aging Anxiety and Body Image

An interventional study of bilinçli farkındalık temelli stres azaltma programı in Body Image, Mindfulness Based Stress Reduction and Middle Aged, sponsored by KTO Karatay University. Not yet recruiting. Open to female participants aged 40 Years to 59 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-25.

Sponsored by KTO Karatay University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Randomized
Ages
40 Years to 59 Years
Sex
Female
01

Study summary

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.
02

Conditions studied

  • Body Image
  • Mindfulness Based Stress Reduction
  • Middle Aged

Keywords

  • aging anxiety
  • middle age woman
  • mindfulness
  • body image
03

In context

Lead sponsor

KTO Karatay University is the lead sponsor of 128 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 59 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • At least primary school graduate,
  • Being between 40-59 years old,
  • Living in Çumra district center,
  • Being open to communication and cooperation

Exclusion criteria

Exclusion Criteria:

  • Those with chronic illnesses (self-report)
  • Foreign nationals Those with psychiatric illnesses (self-report) Those with physical disabilities and limited mobility
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
58 participants (estimated)

Study arms

  • Experimental
    mindfulness-based stress reduction program intervention group

    After the pre-test, a mindfulness-based stress reduction program will be implemented. It will be evaluated with a post-test.

    Behavioral: bilinçli farkındalık temelli stres azaltma programı

  • No intervention
    control group

    A pre-test will be administered. No practice will be conducted. Students will be evaluated with a post-test

Interventions

  • Behavioralbilinçli farkındalık temelli stres azaltma programı

    Following application to the center, the Mindfulness-Based Stress Reduction (MBSR) program will be implemented starting from the scheduled date. The program will last a total of 8 weeks, with one session per week, each session lasting approximately 2 hours. At the end of the 6th week, one day will be designated as a "day of silence," during which a 6-hour session will be conducted. The 8-week program is structured around the themes of aging anxiety and body image. During the day of silent awareness (after the 6th week), the 6-hour silence period will include body scan practices, mindful walking, and breathing meditation. The aim of this silent retreat day is to deepen participants' internal awareness.

06

What researchers measure

Primary outcomes

  1. Change in Aging Anxiety Score as Measured by the Aging Anxiety Scale for Middle-Aged Women

    Aging anxiety will be assessed using the Aging Anxiety Scale for Middle-Aged Women, a self-report questionnaire consisting of Likert-type items. The outcome will be evaluated as the mean change in total scale score from baseline to immediately post-intervention. Higher scores indicate higher levels of aging anxiety.

    Time frame: Baseline and immediately post-intervention (8 weeks)

Secondary outcomes

  1. Change in Body Image Score as Measured by the Body Image Scale

    Body image will be assessed using the Body Image Scale, a self-report instrument measuring individuals' perceptions and attitudes toward their own bodies. The outcome will be evaluated as the mean change in total scale score from baseline to post-intervention. Higher scores indicate a more positive body image.

    Time frame: Baseline and post-intervention (8 weeks)

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Aydın, A., & Kabasakal, E. (2022). Turkish adaptation of the Aging Anxiety Scale for middle-aged women: Validity and reliability study. Journal of Basic and Clinical Health Sciences, 6, 173-180. https://doi.org/10.30621/jbachs.2022.1012 Bergman, Y. S., & Segel-Karpas, D. (2018). Future time perspective, loneliness, and depressive symptoms among middle-aged adults: A mediation model. Journal of Affective Disorders, 241, 173-175. https://doi.org/10.1016/j.jad.2018.08.019 Bergman, Y. S., & Segel-Karpas, D. (2021). Aging anxiety, loneliness, and depressive symptoms among middle-aged adults: The moderating role of ageism. Journal of Affective Disorders, 290, 89-92. https://doi.org/10.1016/j.jad.2021.04.077 Cameron, E., Ward, P., Mandville-Anstey, S. A., & Coombs, A. (2018). The female aging body: A systematic review of female perspectives on aging, health, and body image. Journal of Women & Aging, 31(1), 3-17. https://doi.org/10.1080/08952841.2018.1449586 Creswell, J. D. (2017). Mindfulness interventions. Annual Review of Psychology, 68, 491-516. https://doi.org/10.1146/annurev-psych-042716-051139 Fernandez-Jimenez, C., Alvarez-Hernandez, J. F., Salguero-Garcia, D., Aguilar-Parra, J. M., & Trigueros, R. (2020). Validation of the Lasher and Faulkender Anxiety about Aging Scale (AAS) for the Spanish context. International Journal of Environmental Research and Public Health, 17(12), 4231. https://doi.org/10.3390/ijerph17124231 Gendron, T. L., Inker, J. K., Andricosky, R., & Zanjani, F. (2020). Development of the relational ageism scale: Confirmatory test on survey data. International Journal of Aging and Human Development, 90(3), 281-296. https://doi.org/10.1177/0091415019836956 Lee, H., & You, M. (2019). Development of an aging anxiety scale for middle-aged women. Journal of Korean Academy of Nursing, 49(1), 14-25. https://doi.org/10.4040/jkan.2019.49.1.14

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared due to the sensitive nature of the psychological and health-related information collected from middle-aged women. The dataset includes identifiable variables related to aging anxiety, body image, and mindfulness-based intervention outcomes. Sharing such data may pose confidentiality risks despite anonymization efforts. Aggregated results will be available upon request.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07344896
Responsible party
Sponsor
First posted
Jan 15, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Nov 30, 2026 (estimated)
Completion
May 30, 2027 (estimated)
Last update
Aug 25, 2026

Study contacts

Necibe ş tunalı, master
Contact
necibe.seyda.tunali@karatay.edu.tr
+90 543 242 0280
Necibe Ş TUNALI, 1
study director · KTO KARATAY UNİVERSİTY

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion