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New study: personalized daily tasks beat standard exercise for Seniors' mobility

NCT ID NCT07560098

Symptom relief Sponsor: National Taiwan University Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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

Details not published
The full record has not been published yet, so there is little to show here.
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This status has not been confirmed recently, so it may be out of date.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 looks at two ways to help older adults who are losing mobility: reablement (personalized daily activities) and standard exercise. About 80 seniors from day care centers will take part. The goal is to see which approach better improves movement, reduces fear of falling, and boosts independence.

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

80 people

The number who actually took part.

Started

Dec 2025

Expected to finish

Dec 2026

An estimate. End dates often move.

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

65 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Aged 65 years or older and assessed as Long-Term Care (LTC) need level 2 or above. * Regularly attending adult day care services at least two days per week, with no anticipated termination of services during the study period (approximately three months). * Short Portable Mental Status Questionnaire (SPMSQ) results indicating intact, mild, or moderate cognitive impairment, with the ability to understand simple instructions and participate in activities with assistance. * Able to ambulate independently (assistive devices permitted), with a Short Physical Performance Battery (SPPB) score \< 9, indicating functional decline and high risk of falls. * A score ≥ 9 on the Short Falls Efficacy Scale International (Short FES-I), indicating at least moderate fear of falling. * Willing to participate in the study and able to provide written informed consent. Exclusion Criteria: * History of fracture, major fall, or need for acute medical treatment within the past three months, or deemed by a physician to be unsuitable for moderate or higher levels of physical activity. * Presence of acute psychiatric symptoms that prevent participation in assessments or study procedures. * Severe visual or hearing impairments that interfere with activity participation or assessment. * Currently receiving other intensive rehabilitation or participating in another research intervention. * Demonstrates a clear lack of willingness to participate in the intervention or is unable to complete the three-month observation period.

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As listed by the trial registrant

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

Activities of daily living Elderly Reablement

Contacts and locations

Locations

  • National Taiwan University

    Taipei, Taiwan

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