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Online training could boost confidence for dementia caregivers

NCT ID NCT07690280

Symptom relief Sponsor: Lotung Poh-Ai Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 08, 2026 · Last updated Jul 10, 2026 · Updated 2 times

Summary

This study tests a 6-week web-based program designed to help family caregivers of people with dementia manage behavioral and psychological symptoms like agitation, anxiety, and sleep problems. The program includes educational modules, symptom tracking, and online support. Researchers want to see if it improves caregivers' confidence and reduces their burden compared to usual care alone.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Web-Based Psychoeducation and Symptom-Monitoring Program
What this could lead to
If effective, this program could give family caregivers practical tools to manage dementia-related behaviors and reduce their stress.
What could go wrong
This is a small, early-stage study with 80 participants, so results may not apply to all caregivers. The program requires internet access and may not work for everyone.

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

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

May 2027

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

20 to 90 years

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: 1. Family caregivers aged 20 to 90 years. 2. The primary caregiver of a community-dwelling person diagnosed with dementia. 3. Able to read and understand Chinese. 4. Able to use a smartphone, tablet, or computer with Internet access. 5. Willing to provide written informed consent and comply with study procedures. Exclusion Criteria: 1. Caregivers of persons with dementia who reside in a long-term care institution. 2. Unable to complete study procedures because of cognitive, physical, or communication impairment. 3. Currently participating in another intervention study that may influence the study outcomes.

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Conditions

The condition(s) this trial relates to.

Behavior dementia

As listed by the trial registrant

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

Dementia

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Lotung Poh-Ai Hospital

    RECRUITING

    Luodong, Yilan County, 265, Taiwan

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