Clinical trial registry record

Evolving Methods of Hybrid Exercise-cognition Approach to Promote Health-related Conditions for the Elderly With MCI

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 June 21, 2021.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT03927586
Last registry update
June 21, 2021
Status
Unknown
Phase
Phase not reported
Sponsor
Chang Gung Memorial Hospital
Enrollment
80
Countries
Taiwan
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 · SUPPORTIVE CARE · SINGLE
Evidence population
Human clinical study registration
Participants
80
Population
ALL · 55 Years to 90 Years
Duration
2018-04-10 to 2021-12-01
Intervention
cognitive training; physical exercise training
Comparator
Not reported
Outcomes measured
Change scores of Montreal Cognitive Assessment (MoCA) — Baseline, post test immediately after completing 36 interventio…; Change scores of Verbal fluency test — Baseline, post test immediately after completing 36 intervention sessions (aroun…; Change scores of Wechsler Memory Scale - Third Edition (WMS-III) — Baseline, post test immediately after completing 36…; Change scores of Wechsler Adult Intelligence Scale - Third Edition (WAIS-III) — Baseline, post test immediately after c…; Change scores of Useful Field of View (UFOV) — Baseline, post test immediately after completing 36 intervention session…; Change scores of Stroop Color-Word test — Baseline, post test immediately after completing 36 intervention sessions (ar…; Change scores of Dual-task test — Baseline, post test immediately after completing 36 intervention sessions (around 12…; Change scores of Timed up and go (TUG) — Baseline, post test immediately after completing 36 intervention sessions (aro…; Change scores of Sit-to-stand test — Baseline, post test immediately after completing 36 intervention sessions (around…; Change scores of International Physical Activity Questionnaires (IPAQ) — Baseline, post test immediately after completi…; Change scores of Mobility level — Baseline, post test immediately after completing 36 intervention sessions (around 12…; Change scores of Lower extremity muscle strength — Baseline, post test immediately after completing 36 intervention ses…; Change scores of Grip strength — Baseline, post test immediately after completing 36 intervention sessions (around 12 w…; Change scores of the Barthel Index (BI) — Baseline, post test immediately after completing 36 intervention sessions (ar…; Change scores of Lawton Instrumental Activities of Daily Living Scale (Lawton IADL) — Baseline, post test immediately a…; Change scores of the Disability Assessment for Dementia (DAD) — Baseline, post test immediately after completing 36 int…; Change scores of the Quality of Life in Alzheimer's Disease Instrument (QoLAD) — Baseline, post test immediately after…; Change scores of Community Integration Questionnaire (CIQ) — Baseline, post test immediately after completing 36 interv…; Change scores of Caregiver Burden Inventory (CBI) — Baseline, post test immediately after completing 36 intervention se…; Change scores of Short form of Geriatric Depression Scale (GDS) — Baseline, post test immediately after completing 36 i…
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.

  • Exercise · 100%Title contains controlled topic terminology. Summary contains controlled topic terminology. Source terminology contains a controlled topic term. Title supplies ageing or longevity context.

Automated source check 100% · update recency 50%. These figures help sort records; they are not medical ratings.