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Anxious parents pass it on? new study tests smartphone fix

NCT ID NCT05665491

Knowledge-focused Sponsor: Mclean 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at how parents' tendency to see threats in everyday situations (interpretation bias) may influence their children's anxiety. Researchers will have 300 parents of children aged 7-12 use a smartphone app for four weeks to practice thinking less anxiously. The goal is to see if changing parents' thinking improves parenting behaviors and reduces children's anxiety, paving the way for future treatments.

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 300 people

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

Started

Jul 2023

Expected to finish

Nov 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

7 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 for parent participants are: 1. Must have an ability to speak and understand English sufficiently to complete assessments 2. At least minimal anxiety severity (GAD-7 score \> 5) 3. At least a minimal level of interpretation bias (WSAP overall accuracy less than 70%) 4. No current psychiatric symptoms that would interfere with the individual's ability to provide consent or complete the research procedures 5. If receiving treatment, stable on medications or psychotherapy for 8 weeks 6. No severe suicidal ideation (PHQ-9 item 9 \> 1) 7. Own iOS or Android smartphone 8. Shared or full custody of child (for EMA assessment of parenting behaviors) Inclusion criteria for child participants are: 1. Age 7 to 12 2. Must have an ability to speak and understand English sufficiently to complete assessments 3. No diagnosis of intellectual disability or autism spectrum disorder (per parent or clinician report) 4. No current psychiatric symptoms that would prevent informed consent or understanding of research procedures 5. Wechsler Abbreviated Scale of Intelligence (WASI) full-scale IQ equal to or greater than 80 to ensure understanding of study procedures 6. If receiving treatment, stable on medications or psychotherapy for 8 weeks 7. No severe suicidal ideation (PHQ-9 item 9 \> 1)

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder

As listed by the trial registrant

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

Anxiety

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

  • McLean Hospital

    RECRUITING

    Belmont, Massachusetts, 02478, United States

More trials for these conditions

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