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Brain and body boost: Dual-Task training shows promise for frail seniors

NCT ID NCT07035327

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a 10-week program that combines resistance exercises with cognitive tasks (like memory games) in 38 frail older adults with chronic musculoskeletal pain. The goal was to see if the program is feasible and can improve frailty and thinking skills. Participants were assigned to either the dual-task training or resistance exercise alone. The results will help design larger studies.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

38 people

The number who actually took part.

Started

Jul 2025

Finished

Oct 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

60 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults, of either sex, aged 60 years or above, * living in Hong Kong, being able to read and communicate verbally, * screened frail using the Tilburg Frailty Indicator (TFI) (total score ≥5) with report of memory problems (question 9) (Gobbens et al., 2010), * experiencing any CMP with a pain level higher or equal to 4 in the numerical pain rating scale over a consecutive 3-month period. Exclusion Criteria: Any individuals with either of the following will be excluded: * absence of frailty, * surgical procedure in the lower limbs or the vertebral column; * wheelchair bound or inability to walk for five minutes; * severe balance impairment; * uncompensated cardiac or vascular condition; * acute inflammatory musculoskeletal conditions; * ongoing cancer; dementia; * neurological diseases such as stroke, Parkinson's disease, cerebellar disease, myelopathy, and peripheral neuropathy; * mental illnesses such as schizophrenia, bipolar, psychosis, borderline personality disorder; * illiteracy.

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Conditions

The condition(s) this trial relates to.

agnosia Frailty

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • PolyU Institutional Review Board, The Hong Kong Polytechnic University

    Hong Kong, Hong Kong

More trials for these conditions

Other studies related to the condition(s) this trial covers.