The Effect of a Mindfulness-Based Stress Reduction Program on Feelings of Being a Geriatric Burden in Older Women
THE EFFECT OF A MINDFULNESS-BASED STRESS REDUCTION PROGRAM APPLIED TO ELDERLY WOMEN ON FEELINGS OF BEING A GERIATRIC BURDEN
1 other identifier
interventional
72
1 country
1
Brief Summary
This study was planned as a non-randomized, quasi-experimental study with a pretest-posttest control group design, aiming to examine the effect of a mindfulness-based stress reduction program applied to older women on their feelings of being a geriatric burden. The sample of the study will consist of 72 women aged 60 years and over who have at least one chronic illness, are enrolled in an elderly university program conducted at a foundation university, volunteer to participate in the research, and have no communication difficulties. Data will be collected using a Personal Information Form and the Geriatric Feelings of Burden Scale (GFBS). By investigating the effect of a mindfulness-based stress reduction program on feelings of being a geriatric burden among older women, this study will fill an important gap in the literature. In particular, there is a limited number of studies examining the effectiveness of psychosocial interventions in older age groups, and this research offers a low-cost and feasible approach to enhancing individual well-being. Additionally, the findings obtained from a culturally distinct population will provide original contributions to the international literature in this field.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 15, 2026
CompletedFirst Submitted
Initial submission to the registry
March 26, 2026
CompletedFirst Posted
Study publicly available on registry
March 31, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 4, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 27, 2026
ExpectedMarch 31, 2026
March 1, 2026
3 months
March 26, 2026
March 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Geriatric Feelings of Burdensomeness Scale
The level of geriatric feelings of burdensomeness in older women will be assessed using the Geriatric Feelings of Burdensomeness Scale (GFBS). The scale is a 25-item, self-report instrument rated on a 5-point Likert scale. Total scores range from 25 to 125, with higher scores indicating greater feelings of geriatric burdensomeness. Assessments will be conducted at baseline (pre-test) and after completion of the mindfulness-based stress reduction program (post-test).
2 months
Study Arms (1)
Mindfulness
EXPERIMENTALIntervention and Control Groups Participants will be divided into two groups based on voluntariness and eligibility criteria: Intervention Group: Participants who will take part in the Mindfulness-Based Stress Reduction (MBSR) program. Control Group: Participants who will not participate in the MBSR program but will complete the pretest and posttest assessments. Implementation Process At the beginning of the study, the Geriatric Feelings of Being a Burden Scale will be administered to both groups as a pretest. The intervention group will receive the MBSR program once a week for two weeks, with each session lasting two hours. No intervention will be applied to the control group during this period; they will be asked to continue their routine daily activities. After completion of the program, the same scale will be re-administered to both groups to obtain posttest data. Intervention Content (MBSR Program) Mindfulness meditation Body scan exercises Conscious breathing awarene
Interventions
Intervention and Control Groups Participants will be divided into two groups based on voluntariness and eligibility criteria: Intervention Group: Participants who will take part in the Mindfulness-Based Stress Reduction (MBSR) program. Control Group: Participants who will not participate in the MBSR program but will complete the pretest and posttest assessments. Implementation Process At the beginning of the study, the Geriatric Feelings of Being a Burden Scale will be administered to both groups as a pretest. The intervention group will receive the MBSR program once a week for two weeks, with each session lasting two hours. No intervention will be applied to the control group during this period; they will be asked to continue their routine daily activities. After completion of the program, the same scale will be re-administered to both groups to obtain posttest data. Intervention Content (MBSR Program) Mindfulness meditation Body scan exercises Conscious breathing awarenes
Eligibility Criteria
You may qualify if:
- Women aged 60 years or older
- Having at least one chronic disease
- Enrolled in a senior university program at a foundation university
- Willing to participate in the study
- Able to communicate without any problems
You may not qualify if:
- Individuals who do not voluntarily agree to participate in the study
- Individuals with communication difficulties (e.g., severe hearing loss, speech disorder, advanced cognitive impairment)
- Individuals with serious psychiatric or neurological disorders that prevent participation
- Individuals who show severe emotional distress or agitation during the interview
- Individuals with difficulty speaking or understanding Turkish
- Individuals who do not have sufficient time to actively participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Aydın Universty
Istanbul, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 26, 2026
First Posted
March 31, 2026
Study Start
January 15, 2026
Primary Completion
April 4, 2026
Study Completion (Estimated)
May 27, 2026
Last Updated
March 31, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share