NCT07502547

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
0mo left

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress97%
Jan 2026May 2026

Study Start

First participant enrolled

January 15, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 26, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 31, 2026

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 4, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 27, 2026

Expected
Last Updated

March 31, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

March 26, 2026

Last Update Submit

March 26, 2026

Conditions

Keywords

MindfulnessGeriatric Burden AmongOlder Women

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

EXPERIMENTAL

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 awarene

Behavioral: Mindfulness meditation

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

Mindfulness

Eligibility Criteria

Age60 Years+
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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)

Location

MeSH Terms

Interventions

Mindfulness

Intervention Hierarchy (Ancestors)

Cognitive Behavioral TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

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

Locations