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Acupoint Stimulation and Exercise for Taiwanese Pre-frail Older Adults

Exploring the Associations Among Frailty, Daily Physical Activity, Sleep, and Traditional Chinese Medicine Constitution in Taiwanese Older Adults, and Evaluating the Effects of Acupoint Stimulation Interventions

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07732530
Enrollment
30
Registered
2026-07-29
Start date
2025-06-03
Completion date
2027-12-31
Last updated
2026-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty, Sleep Quality, Aging

Brief summary

This study aims to explore the relationships between frailty, daily physical activity, sleep quality, and Traditional Chinese Medicine (TCM) constitutions among older adults in Taiwan. In the trial phase, a randomized controlled trial will be conducted specifically for pre-frail older adults. Participants will be randomly assigned to either the exercise training group (Vivifrail program) or the integrated group combining exercise with daytime and sleep-improving acupoint stimulation. The study evaluates the combined efficacy of these non-invasive interventions on reducing frailty severity, improving sleep, and enhancing daily physical functions.

Interventions

A 12-week home-based multimodal exercise program including daily walking, upper limb resistance training, balance exercises, and flexibility training, tailored to pre-frail older adults.

Daily home-based acupoint self-massage (2-3 times per day, 3-5 minutes per point) targeting specific meridians (including Spleen, Stomach, and Bladder meridians) to alleviate fatigue and promote sleep quality.

Sponsors

Tainan Hospital, Ministry of Health and Welfare
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Individuals who are capable of undergoing frailty assessments. 2. Individuals who possess effective communication skills. 3. Aged 50 years or older. 4. Willing to provide written informed consent, keep a 7-day sleep diary, and complete related questionnaires. 5. Identified as pre-frail (frailty score of 1-2 points) according to the frailty phenotype criteria for the clinical trial phase.

Exclusion criteria

1\. Individuals who are unwilling or unable to wear an actigraph (wrist monitor) or undergo physical measurements.

Design outcomes

Primary

MeasureTime frameDescription
Change in Frailty ScoreBaseline, Week 4, and Week 12Evaluated using the Fried frailty phenotype criteria, which includes five components: unintentional weight loss, weakness (grip strength), exhaustion, slowness (walking speed), and low physical activity. Each component is scored as 0 or 1, resulting in a total score ranging from 0 to 5. Higher scores indicate a worse outcome (higher severity of frailty).
Change in Sleep QualityBaseline, Week 4, and Week 12Measured via the Pittsburgh Sleep Quality Index (PSQI) questionnaire (global score ranges from 0 to 21, where higher scores indicate poorer sleep quality) and objective metrics from the 7-day wrist actigraphy (including total sleep time and sleep efficiency).

Countries

Taiwan

Contacts

CONTACTYu-Ching Hsu, MD
tnhpcm2017@gmail.com+886-6-2202121

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026