Clinical trial registry record

A Dyadic e-Health System on Enhancing Healthy Lifestyles of Older Adults With Sarcopenia

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Unknown.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated March 22, 2024.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT06088511
Last registry update
March 22, 2024
Status
Unknown
Phase
Phase not reported
Sponsor
The Hong Kong Polytechnic University
Enrollment
88
Countries
Hong Kong
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · SINGLE
Evidence population
Human clinical study registration
Participants
88
Population
ALL · 60 Years
Duration
2024-05-06 to 2026-01-01
Intervention
e-Health System with nutritional advice; The Exercise Training
Comparator
The Control Group
Outcomes measured
Changes of muscle strength — Change from baseline to 4 weeks immediately after the completion of all supervised session…; Changes of muscle mass — Change from baseline to 4 weeks immediately after the completion of all supervised sessions, 1…; Changes of body mass index — Change from baseline to 4 weeks immediately after the completion of all supervised session…; Changes of waist circumference — Change from baseline to 4 weeks immediately after the completion of all supervised ses…; Changes of fat mass — Change from baseline to 4 weeks immediately after the completion of all supervised sessions, 12 w…; The Short Physical Performance Battery (SPPB) scale — Change from baseline to 4 weeks immediately after the completion…; Mini Nutritional Assessment (MNA) Short-form — Change from baseline to 4 weeks immediately after the completion of all…; Health Action Process Approach (HAPA) Nutrition Self-efficacy Scale — Change from baseline to 4 weeks immediately after…; Dietary quality index-International (DQI-I) — Change from baseline to 4 weeks immediately after the completion of all s…; Diet Adherence — Change from baseline to 4 weeks immediately after the completion of all supervised sessions, 12 weeks…; Exercise Adherence — Change from baseline to 4 weeks immediately after the completion of all supervised sessions, 12 we…; Changes of Numeric Rating Scale (NRS) — Change from baseline to 4 weeks immediately after the completion of all supervi…; Changes of Brief Fatigue Inventory (BFI) — Change from baseline to 4 weeks immediately after the completion of all supe…; Changes of Chinese Self-Efficacy for Exercise (CSEE) scale — Change from baseline to 4 weeks immediately after the comp…; Changes of Fried Frailty Index (FFI) — Change from baseline to 4 weeks immediately after the completion of all supervis…; Changes of the 15-item Chinese version Geriatric Depression Scale (C-GDS) — Change from baseline to 4 weeks immediately…; Changes of the Chinese (Hong Kong) 12-item Short Form Health Survey (SF-12v2) — Change from baseline to 4 weeks immedia…; Changes of the Strength, Assistance in walking, Rise from a chair, Climb stairs, and Falls (SARC-F) — Change from basel…
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Sarcopenia · 100%Title contains controlled term: sarcopenia. Abstract contains controlled term: sarcopenia. Source terminology contains: sarcopenia. Title supplies longevity context: older adult. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.