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App-Based support boosts caregiver Well-Being in pilot study

NCT ID NCT05992467

What the study statuses mean

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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 Results may not be published yet.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

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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a mobile health program called WECARE for Chinese American family caregivers of people with dementia. 48 caregivers received daily multimedia content on WeChat for 7 weeks, designed to improve caregiving skills and self-care. The goal was to see if the program could reduce depressive symptoms and caregiving burden.

What this could mean

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

Active substance
Wellness Enhancement for Caregivers (WECARE) behavioral intervention delivered via WeChat
What this could lead to
If it works, this could point toward a practical, low-cost way to support dementia caregivers and reduce their stress and depression.
What could go wrong
This is a small pilot study with only 48 participants, so results may not apply to all caregivers. The intervention is behavioral, so benefits may be modest and hard to sustain long-term.

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

48 people

The number who actually took part.

Started

Sep 2023

Finished

Aug 2024

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

21 to 90 years

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: 1. 21 years or older, 2. self-identified as Chinese or Chinese American, 3. speak and read Chinese (Mandarin or Cantonese), 4. own a smartphone and use WeChat, 5. living in Washington DC metropolitan, and 6. currently care for a family member with ADRD and provide care for at least 10 hours a week. Exclusion Criteria: 1. do not read or speak Chinese, 2. care-recipient is in hospice care or have a life expectancy less than 6 months, 3. signs of severe intellectual deficits or psychotic disorders, or 4. unable to provide informed consent.

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Conditions

The condition(s) this trial relates to.

Caregiver Burden

As listed by the trial registrant

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

Contacts and locations

Locations

  • George Mason University

    Fairfax, Virginia, 22030, United States

More trials for these conditions

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