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Not yet recruiting NCT07025655

Effectiveness of a Mindfulness and Digital Technology Program for Healthy Aging (MMP-DTLA)

No phase Interventional Mindfulness Healthy Aging

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Multifaceted Mindfulness Program, Placebo.
Who it may be relevant to
Registry conditions: Mindfulness, Healthy Aging. Basic parameters: from 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Effectiveness of a Multifaceted Mindfulness Program Integrated With Digital Technology-Assisted Learning on Healthy Aging in Community-Dwelling Older Adults: A Randomized Controlled Trial

Overview

This study aims to evaluate the effectiveness of a mindfulness program integrated with digital technology-assisted learning on healthy aging among community-dwelling older adults. In a randomized controlled trial, 100 participants will be randomly assigned to either an experimental or a control group. The experimental group will receive a ten-week mindfulness program supported by digital tools such as educational videos and LINE Bot messaging. Primary outcomes include mindfulness awareness, physical activity, heart rate variability, cognitive function, sleep quality, perception of aging, and healthy aging perspectives. Additionally, qualitative interviews will be conducted with 10 experimental group participants to explore their intervention experiences.

Interventions

  • Behavioral Multifaceted Mindfulness Program
    Ten-week mindfulness classes
  • Behavioral Placebo
    Regular daily activity

Primary outcome measures

  • mindfulness awareness [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Physical activity: PASE-C [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Physical activity: SPPB [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Cognitive function [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Heart rate variability: SDNN [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Heart rate variability: LF/HF ratio [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Sleep quality [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Perception of ageing [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]
  • Healthy ageing perspectives [Time frame: We will collect four times of data: 1. Baseline 2. The fourth week 3. Up to 10 weeks 4. After completing the study for one month]

Eligibility criteria

Inclusion criteria

  • ability to communicate in Mandarin or Taiwanese
  • aged 65 years or older in the community
  • Currently using a mobile phone and the LINE application as a means of communication.

Exclusion criteria

  • Individuals with cognitive impairments
  • Unable to communicate verbally

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Publications

  • Wang YR, Lee HF, Hsieh PL, Chang CH, Chen CM. Relationship between physical activity and perceptions of ageing from the perspective of healthy ageing among older people with frailty with chronic disease: a cross-sectional study. BMC Nurs. 2023 Sep 16;22(1):319. doi: 10.1186/s12912-023-01481-9. PMID 37716946

Identifiers

NCT: NCT07025655 · 202400087B0C6001 · NSTC 113-2410-H-255 -001 -MY2

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗