NCT07540117

Brief Summary

This study evaluates the effects of a social prescribing intervention on health promotion outcomes in community-dwelling older adults. The intervention consists of a 4-week mindfulness meditation program followed by a 12-week walking-pole exercise program. The purpose of the study is to determine whether this combined intervention improves physical function, psychological well-being, and sleep quality. Eligible participants aged 55 years and older will be enrolled from community settings and will receive the same 16-week intervention. Assessments will be conducted at baseline, after the mindfulness phase, after completion of the full intervention, and 3 months after the intervention ends. Study outcomes include physical function, mood, well-being, sleep quality, and indicators of continued participation and lifestyle change. The investigators hypothesize that the combined social prescribing intervention will lead to improvements in physical and psychological health among community-dwelling older adults and support healthy aging.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
1,500

participants targeted

Target at P75+ for not_applicable

Timeline
35mo left

Started Apr 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
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 Progress2%
Apr 2026Apr 2029

First Submitted

Initial submission to the registry

April 13, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

April 14, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 20, 2026

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2029

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2029

Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

3 years

First QC Date

April 13, 2026

Last Update Submit

April 20, 2026

Conditions

Keywords

Social PrescribingMindfulness MeditationWalking Pole ExerciseOlder AdultsCommunity-Dwelling Older AdultsHealthy AgingHealth PromotionPsychological Well-BeingSleep QualityPhysical Function

Outcome Measures

Primary Outcomes (1)

  • Five Times Sit-to-Stand Test

    Time in seconds required to complete the Five Times Sit-to-Stand Test, used to assess lower-extremity muscle strength and functional mobility. Lower values indicate better performance.

    Baseline, at Week 5, and at Week 17

Study Arms (1)

Mindfulness Meditation Plus Walking-Pole Exercise

EXPERIMENTAL
Behavioral: Mindfulness Meditation and Walking-Pole Exercise

Interventions

1. Mindfulness Meditation A 4-week group-based mindfulness meditation program delivered once weekly for approximately 60 minutes per session. The program includes breathing awareness, body awareness, relaxation training, emotion regulation, and positive psychological practices. Sessions are conducted in person by trained instructors and are supported by guided home practice using audio content. The purpose of this phase is to promote psychological well-being, relaxation, sleep improvement, and self-regulation before the exercise phase begins. 2. Walking-Pole Exercise A 12-week group-based walking-pole exercise program delivered once weekly for approximately 60 to 90 minutes per session. The program includes warm-up, structured walking-pole exercise, cool-down, and brief calming or meditative practice. It focuses on muscle strengthening, balance training, mobility, functional movement, and health promotion activities relevant to older adults. Sessions are led by qualified instructors,

Mindfulness Meditation Plus Walking-Pole Exercise

Eligibility Criteria

Age55 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adults aged 55 years and older
  • Community-dwelling older adults
  • Able to walk independently or with assistive devices
  • Normal cognitive function or mild cognitive impairment, with ability to understand and follow study procedures
  • Willing to sign informed consent
  • Willing to participate in the intervention and complete study assessments

You may not qualify if:

  • Major surgery or hospitalization within the previous 3 months
  • Severe cardiovascular disease or other medical condition making exercise inappropriate, based on physician assessment
  • Moderate to severe dementia or other severe psychiatric disorder
  • Inability to comply with the 4-week mindfulness meditation program or the 12-week walking-pole exercise program

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Health Research Institutes

Zhunan, Miaoli, 350, Taiwan

RECRUITING

MeSH Terms

Conditions

Psychological Well-BeingSleep Initiation and Maintenance Disorders

Interventions

Mindfulness

Condition Hierarchy (Ancestors)

Personal SatisfactionBehaviorSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Intervention Hierarchy (Ancestors)

Cognitive Behavioral TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Central Study Contacts

Ren-Hua Chung, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 13, 2026

First Posted

April 20, 2026

Study Start

April 14, 2026

Primary Completion (Estimated)

April 1, 2029

Study Completion (Estimated)

April 1, 2029

Last Updated

April 23, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared because the study involves community-dwelling older adults and includes sensitive personal and health-related information. To protect participant privacy and comply with institutional review board and data protection requirements, no individual-level de-identified dataset is currently planned for public sharing. Study findings will be reported in aggregate form only.

Locations