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Implementation ScienceBENEFITSNCT06601062

Leveraging Telepsychology and Behavioral Economics to Increase Fidelity to CBT

A study testing Tele-BE in people with Implementation Science, run by University of Pennsylvania at 1 site in United States.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

The goal of this study is to develop and test a telehealth tool intended to support community mental health clinicians to deliver cognitive behavioral therapy (CBT). The main aims of the study are to: 1. Read more about this study

Who is it for?
Ages 14 years and olderHealthy volunteers can take part
Conditions the study is for
Implementation Science
What is being tested?
Tele-BE
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteUnited States
Study dates
4 Mar 2025to 30 Apr 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 14 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • 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
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  • 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

Who cannot join

  • 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
Show all 13Show fewer
  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site
  • University of Pennsylvania

    Philadelphia, Pennsylvania, 19104

Other trials in United States

About this study

The goal of this study is to develop and test a telehealth tool intended to support community mental health clinicians to deliver cognitive behavioral therapy (CBT).

The main aims of the study are to:

  1. Collaborate with clinicians and supervisors to design an accessible prototype to increase clinician use of CBT in community mental health settings through focus groups, interviews, and surveys.
  2. Adapt the initial model through feedback from clinicians and their patients who will be asked to test the tool then complete interviews and surveys.
  3. Test the model with clinicians and their patients who will be asked to use the tool for several weeks.
  4. Evaluate the acceptability and feasibility of using the tool in a pilot trial through surveys and interviews.
Read the detailed description

Our primary goal in this exploratory project is to develop, iteratively, refine and evaluate the preliminary effectiveness, acceptability, and feasibility of "Tele-BE," a novel telehealth platform that integrates behavioral economics (BE) strategies into the clinician user-interface of standard telehealth technology, to increase clinician use of structural components of cognitive behavioral therapy (CBT). Primary endpoints for this study are the refined Tele-BE platform implementation strategy and evaluation of Tele-BE's preliminary effectiveness to increase clinician fidelity and acceptability, and feasibility. Secondary outcomes include target implementation mechanisms (clinician intentions and their determinants: attitudes, norms and self-efficacy) consistent with our conceptual model. Our primary hypotheses are that Tele-BE will increase clinician fidelity to CBT structural components during the observation period and that Tele-BE will be an acceptable and feasible implementation strategy. Secondary hypotheses are that Tele-BE will engage our target implementation mechanisms of interest, as delineated in Table 1 of the Research Strategy. Of note, as this is a pilot trial, it is not intended to be fully powered to detect effects and we will rely on qualitative and mixed methods analyses to examine study hypotheses.

Our goal is to develop and pilot-test Tele-BE to nudge clinicians to deliver six CBT structural components of interest: (1) symptom monitoring, (2) agenda setting guided by shared decision-making, (3) out-of-session practice ("homework") review, (4) skill instruction, (5) skill practice, and (6) homework planning. Tele-BE will leverage the infrastructure of standard telehealth platforms to alter the clinician interface and incorporate behavioral economics (BE) strategies to make it easier and more motivating to deliver structural components of interest to patients. We will partner with BlueJeans by Verizon, who currently partners with Penn Medicine to support HIPAA compliant telehealth technology throughout the system, to create the Tele-BE prototype that will be tested in this study.

In Aim 1, we will adapt and refine Tele-BE in collaboration with a Stakeholder Advisory Board, BlueJeans, and Transmogrify, a web development company with an established partnership with Penn Medicine. Aim 1 is a largely preparatory aim during which we will refine our Tele-BE prototype in collaboration with an initial group of 3 community clinicians as our target end-users as well as 3 clinical supervisors. We will recruit three additional clinicians in Aim 1 to test out early elements of Tele-BE. These additional clinicians will engage in laboratory-based usability testing with a basic functional version of Tele-BE. Participants will meet with the study team and interact with the Tele-BE platform for 30 minutes; participants also will conduct a mock therapy session with a graduate student clinician. Participants will be recorded through the BlueJeans platform while interacting with Tele-BE. We will use a "think aloud" framework to have clinicians verbalize their thoughts when using the program. Following the think aloud protocol, participants will complete brief questionnaires and a brief interview to inform Tele-BE refinement.

In Aim 2, we will work closely with our web development team to field test and iteratively refine Tele-BE using rapid cycle prototyping to optimize the user experience and refine our specific BE strategies. We anticipate recruiting 5 community clinicians and 5 of their patients to pilot iterations of Tele-BE in their clinical practice for 4-5 weeks. These participants will provide qualitative feedback on Tele-BE's ability to engage target implementation mechanisms. if saturation is not reached with an initial sample of participants, we may recruit up to 5 more clinician and patient dyads. The primary outcome of Aim 2 will be a refined version of Tele-BE to be tested in the pilot trial.

Aim 3 is a pilot 16-week open trial to test preliminary effectiveness of the refined Tele-BE to enhance clinician CBT structural component fidelity. We will recruit 30 community mental health clinicians and randomize them to Tele-BE or telehealth as usual (Tele-AU). The trial will include 2 patients per clinician (60 patients total). Note that the exact features included in Tele-BE will be dependent on the outcomes of Aims 1 and 2 and are not designed to change clinician session content (i.e., the specific intervention techniques a clinician employs) in any way. However, we anticipate that it will include some or all of the following design features: (1) Reminder message prompting clinician to identify a skill to review, introduce, or practice, prior to the start of a clinical encounter, (2) Completion of progress measures (in this case, measures of therapeutic alliance) in the telehealth "waiting room," (3) Template agenda of structural components with an option to select CBT interventions that will be delivered in session, (4) Checkmarks indicating the CBT component is completed, with a display that adjusts as goals are reached, (5) Gamification features (e.g., badges) for goals met (e.g., agenda completed >90% of the time), (6) Feedback messages about elements completed from clinical supervisor (e.g., messages offering praise for hitting certain benchmarks, and (7) Downloadable summary of session activities for the clinical progress note. All therapy sessions will be recorded and subsequently coded for fidelity (Aim 3 primary outcomes). Clinicians will complete measures of intentions and their determinants at the week of sessions 1, 5, 9, and 12 (Aim 3 secondary outcomes).

Using data from the open trial, Aim 4 will examine acceptability and feasibility of Tele-BE from patient and clinician perspectives and potential ethical issues with Tele-BE. We will measure Tele-BE acceptability and feasibility via web analytics, surveys, interviews, and recruitment and retention statistics, and patient outcomes. Patients will complete self-report measures of therapeutic alliance and symptoms on the same schedule as clinician report; they additionally will complete measures of patient centered care at pre and post. Select patients will also complete qualitative interviews.

To recruit and enroll clinicians, we first will identify a minimum of 4 Philadelphia agencies that are already using telehealth and are trained in transdiagnostic CBT through the Penn Collaborative for CBT and Implementation Science (directed by MPI Dr. Creed). While the telehealth landscape will likely shift as the COVID-19 pandemic ebbs, Philadelphia's Medicaid behavioral health payor has committed to continuing to reimburse for telehealth after the crisis concludes. We then will employ a cascaded recruitment strategy to recruit 30 clinicians who then will identify their patients aged 14 or older (the age of consent for mental health services in Pennsylvania) with whom they are providing psychotherapy via telehealth. We will work with clinicians to identify two patients that they will approach for study participation. For each clinician-patient dyad, participation will occur over a 16-week trial period. Clinicians and patients will complete study measures as outlined in Table 3 of the Research Strategy.

Being tested
Tele-BE

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Tele-BEDevice

    Clinicians and their patients use the newly developed telehealth tool to support their use of CBT during session

Study groups in NCT06601062
Study groupRoleWhat they receive
Treatment as usualNo interventionClinicians will deliver cognitive behavioral therapy as usual, as consistent with routine clinic practices, to patients receiving telehealth services
Tele-BEExperimentalClinicians will deliver cognitive behavioral therapy as usual, as consistent with routine clinic practices, with the support of the Tele-BE platform, to patients receiving telehealth services
Receives: Device: Tele-BE

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Acceptability of Tele-BE

    Acceptability of Intervention Measure: A 4-item, psychometrically-validated measure that indexes the extent to which stakeholders believe an implementation strategy is acceptable Qualitative Interview

    Measured: Week of sessions 1, 5, 9, and 12

  2. Feasibility of Tele-BE

    Feasibility of Intervention Measure; A 4-tem, psychometrically-validated measure that indexes the extent to which stakeholders perceive an implementation strategy is feasible Web Analytics (i.e., clinician use of Tele-BE features)

    Measured: Week of sessions 1, 5, 9, and 12

  3. Usability of Tele-BE

    • System Usability Scale (SUS): A 10-item questionnaire on a 5-point scale from 1=Strongly disagree to 5=Strongly agree which measures the usability of a system (in this case, Tele-BE).

    Measured: Week of sessions 1, 5, 9, and 12

  4. Clinician Fidelity to CBT Structural Components

    Cognitive Therapy Rating Scale (CTRS): Clinician fidelity to structural components will be captured via direct observation to each of the 6 components of interest: ((1) progress monitoring with evidence-based assessment tools, (2) agenda setting guided by shared decision-making, (3) out-of-session practice ("homework") review, (4) skill instruction, (5) skill practice, and (6) homework planning. Items will be coded using adapted items of the CTRS, a gold-standard CBT fidelity measure that has a subscale designed to measure structural components

    Measured: Weekly over the trial period (approximately 12 sessions, up to 16 weeks)

Secondary outcomes (4)
  1. Clinician intentions to use the 6 structural components of EBPs of interest

    Established question stems from behavioral science using two items on a 7-point scale asking how willing and how likely one is to use each structural component

    Measured: Week of sessions 1, 5, 9, and 12

  2. Clinician attitudes, norms, and self-efficacy (i.e., determinants of intentions) to use the 6 structural components of EBPs of interest

    Established question stems from behavioral science, all measured on a 7-point scale. The total scale score will be computed by averaging all z-standardized items within each structural component. Attitudes are measured on the extent to which clinicians agree/disagree with each statement (higher score indicates more favorable attitude). Norms are measured on a scale of degree of agreement regarding the perception that "other people like me" will use the component, and that other people who are important to them (e.g., supervisors) will approve of them using it. Self-efficacy is measured on degree of agreement about clinicians' perceptions of themselves as having the ability to perform each component.

    Measured: Week of sessions 1, 5, 9, and 12

  3. Patient clinical symptoms

    Patient symptoms will be measured with the Strengths and Difficulties Questionnaire, a broadband questionnaire of self-reported mental health symptoms

    Measured: Week of sessions 1, 5, 9, and 12

  4. Therapeutic alliance

    The Working Alliance Inventory-Short Form (WAI-SF) is a validated measure that asks patients to rate 12 items regarding their perceptions of their relationship with their therapist using a 5-point Likert scale

    Measured: Week of sessions 1, 5, 9, and 12

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Sep 2024
  2. Study start4 Mar 2025
  3. Primary completion1 Feb 2027 (estimated)
  4. Study completion30 Apr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06601062
Sponsor's protocol ID
R34MH135965
Acronym
BENEFITS
Status last verified
Apr 2026
First submitted
15 Aug 2024
Last updated
5 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Publications

  • Becker-Haimes EM, Mandell DS, Kuo PB, Lynch KG, Brady M, Young S, Creed TA. Behavioral Nudges to Enhance Fidelity in Telehealth Sessions (BENEFITS): Protocol for Developing and Pilot Testing a Telehealth Tool to Improve Cognitive Behavioral Therapy Implementation. JMIR Res Protoc. 2025 Sep 18;14:e76035. doi: 10.2196/76035.

    PubMed 40966682

Questions about this trial

What is this clinical trial studying?

A study testing Tele-BE in people with Implementation Science, run by University of Pennsylvania at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 28 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Acceptability of Tele-BE (time frame: Week of sessions 1, 5, 9, and 12). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06601062, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2026.

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