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New telehealth tool aims to help therapists stick with CBT

NCT ID NCT06601062

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 is developing and testing a telehealth tool to support community mental health clinicians in using cognitive behavioral therapy (CBT) with their patients. Researchers will work with about 100 clinicians and their patients to design, refine, and evaluate the tool through interviews, surveys, and a pilot trial. The goal is to see if the tool is acceptable, feasible, and helps clinicians deliver CBT more consistently.

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 100 people

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

Started

Mar 2025

Expected to finish

Apr 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

14 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: Prototyping open trial phase: Clinician Participants * Clinician is an outpatient mental health clinician in the City of Philadelphia trained in transdiagnostic CBT through the Penn Collaborative for CBT and Implementation Science * Clinician has completed the 22-hour intensive CBT workshop through the BCI or equivalent CBT training * Clinician provides direct mental health services to a treatment-seeking population via telehealth * Proficient in English language * Has access to a computer with internet connectivity Patient Participants * Patient is 14 years or older * Patient is receiving CBT from a participating clinician * Patient is able to provide informed consent (or if the client is between the ages of 14-17, the client is able to assent and has a legal guardian who is able to provide consent) * Proficient in English language * Patient has had at least one prior telehealth therapy session with enrolled therapist * Has access to a computer with internet connectivity or smartphone through which they regularly attend telehealth therapy sessions Pilot randomized controlled trial phase: Clinician Participants * Clinician is an outpatient mental health clinician in the City of Philadelphia trained in transdiagnostic CBT through the Penn Collaborative for CBT and Implementation Science * Clinician has completed the 22-hour intensive CBT workshop through the BCI or equivalent CBT training * Clinician is a practicing mental health clinician in the Philadelphia region in one of our partner local community agencies delivering telehealth services * Clinician has at least 2 clients on their caseload over the age of 14 with whom they are delivering CBT telehealth services * Proficient in English language * Has access to a computer with internet connectivity Patient Participants * Patient is 14 years or older * Patient is able to provide informed consent (or if the client is between the ages of 14 -17, the client is able to assent and has a legal guardian who is able to provide consent) * Proficient in English language * Patient has had at least one prior telehealth therapy session with enrolled therapist * Has access to a computer with internet connectivity or smartphone through which they regularly attend telehealth therapy sessions Exclusion Criteria: Prototyping open trial phase: Clinician Participants - Clinician does not provide any telehealth services. Patient Participants * Patients will be excluded if they are unable to adequately consent to study procedures. For example, clients may be excluded if they are at imminent risk for suicide or homicide requiring hospitalization. * Youth under the age of 18 will be excluded from the study if they do not have an available legal guardian who is able to provide consent for their study participation (e.g., the state has legal custody of the youth). * Patients under the age of 14 will be excluded Pilot randomized controlled trial phase: Participants will not be excluded based on sex, demographics, and or past experience. Clinician Participants \- Clinician does not provide telehealth services to at least 2 individuals on their caseload. Patient Participants * Patients will be excluded if they are unable to adequately consent to study procedures. For example, clients may be excluded if they are at imminent risk for suicide or homicide requiring hospitalization or are experiencing any cognitive impairment that prevents them from participating in therapy on the day their session is to be recorded. * Youth under the age of 18 will be excluded from the study if they do not have an available legal guardian who is able to provide consent for their study participation (e.g., the state has legal custody of the youth). * Patients under the age of 14 will be excluded

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As listed by the trial registrant

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

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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

  • University of Pennsylvania

    Philadelphia, Pennsylvania, 19104, United States

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