Improving Quality of Care in Child Mental Health Service Settings

Sponsor
Medical University of South Carolina (Other)
Overall Status
Recruiting
CT.gov ID
NCT03305458
Collaborator
(none)
360
1
2
51
7.1

Study Details

Study Description

Brief Summary

The investigators recently completed an NIMH R34 in which they piloted a patient- and provider-informed tablet-based toolkit designed to facilitate delivery of Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) - a treatment that was selected because it addresses a wide range of symptoms using techniques shared by other treatments for emotional and behavioral disorders. The tablet-based toolkit consists of numerous components (e.g., videos, interactive games, drawing applications) that are designed to facilitate provider-patient interactions in a way that enhances children's engagement and supports adherence to the treatment model. The tablet-based toolkit was very well received by children, caregivers, and providers in the pilot evaluation. Moreover, all benchmarks for feasibility were met or exceeded. This study proposes to conduct a hybrid effectiveness-implementation trial to examine the extent to which the tablet intervention may improve fidelity, engagement, and children's mental health outcomes. The investigators will conduct a randomized controlled trial with 120 mental health providers and 360 families in partnership with dozens of clinics in the Carolinas and Florida. Providers will be assigned randomly to tablet-facilitated vs. standard TF-CBT. Youth aged 8-16 years with clinically elevated symptoms of PTSD will be recruited. Baseline and 3-, 6-, 9-, and 12-month post-baseline assessments will be conducted by independent, blind evaluators. Sessions will be videorecorded for observational coding of engagement and fidelity by independent raters blind to study hypotheses. The investigators will also examine costs and conduct semi-structured interviews with families, providers, supervisors, and agency leaders to inform future dissemination and implementation initiatives. Technology-based resources that are scalable, easy to use, and designed for efficient integration into everyday practice may have sustained national impact.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: TFCBT
  • Behavioral: eTFCBT
N/A

Detailed Description

Assuring children access to the highest quality mental health care is a top national priority. Yet, quality of care continues to be highly variable in traditional service settings. Novel, scalable solutions are needed to address modifiable quality-of-care indicators in sustainable ways. To this end, provider fidelity and children's engagement are key correlates of clinical outcome and practical targets for intervention. There is tremendous opportunity to address both through technology. Studies in child education show that interactive games, touch-screen learning, and demonstration videos enhance engagement, knowledge, motivation, and learning. These benefits also may extend to the therapeutic context, where strategic integration of technology-based activities may enhance children's learning, strengthen the therapeutic alliance, and keep providers on protocol. The investigators recently completed an NIMH R34 in which they piloted a patient- and provider-informed tablet-based toolkit designed to facilitate delivery of Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) - a treatment that was selected because it addresses a wide range of symptoms using techniques shared by other treatments for emotional and behavioral disorders. The tablet-based toolkit consists of numerous components (e.g., videos, interactive games, drawing applications) that are designed to facilitate provider-patient interactions in a way that enhances children's engagement and supports adherence to the treatment model. The tablet-based toolkit was very well received by children, caregivers, and providers in the picot evaluation and all benchmarks for feasibility were met or exceeded. The investigators propose to conduct a hybrid effectiveness-implementation trial to examine the extent to which the tablet intervention may improve fidelity, engagement, and children's mental health outcomes. The investigators will conduct a randomized controlled trial with 120 mental health providers and 360 families in partnership with dozens of clinics in the Carolinas and Florida. Providers will be assigned randomly to tablet-facilitated vs. standard TF-CBT. Youth aged 8-16 years with clinically elevated symptoms of PTSD will be recruited. Baseline and 3-, 6-, 9-, and 12-month post-baseline assessments will be conducted by independent, blind evaluators. Sessions will be videorecorded for observational coding of engagement and fidelity by independent raters blind to study hypotheses. The investigators will also examine costs and conduct semi-structured interviews with families, providers, supervisors, and agency leaders to inform future dissemination and implementation initiatives. Technology-based resources that are scalable, easy to use, and designed for efficient integration into everyday practice may have sustained national impact.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
360 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Improving Quality of Care in Child Mental Health Service Settings
Actual Study Start Date :
Oct 1, 2018
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Treatment as usual

Trauma Focused Cognitive Behavioral Therapy

Behavioral: TFCBT
treatment as usual

Experimental: Tablet-Facilitated TF-CBT

Standard treatment with the addition of in-treatment/session iPad activities

Behavioral: eTFCBT
tablet-facilitated Trauma Focused Cognitive Behavioral Therapy (eTFCBT)

Outcome Measures

Primary Outcome Measures

  1. Child Involvement Ratings Scale [will be assessed throughout the course of treatment (expected to be 12-20 weeks in duration for each participant)]

    Child engagement will be measured via coding of audiotaped sessions by independent, trained raters who are blind to study purpose and hypotheses. The Child Involvement Ratings Scale (CIRS), a 6-item scale that measures child engagement for each session, will be used. Four "positive" involvement items and two "negative" involvement items are rated for each session on a 6-point scale ("not at all" to "a great deal" present). The positive-involvement items emphasize the extent to which children initiate discussions, demonstrate enthusiasm, self-disclose, and demonstrate understanding. Negative-involvement items address withdrawal or avoidance in treatment. Coders provide ratings based on two 10-min segments of session audiotapes (beginning at min 10 and min 40).

  2. Provider Treatment Fidelity [will be assessed throughout the course of treatment; an expected duration of 12-20 weeks]

    Fidelity to the TF-CBT protocol will be measured via coding of videotaped treatment sessions by independent, trained raters who are blind to study purpose and hypotheses. Ratings will be completed using the TF-CBT Version of the Therapy Process Observational Coding System for Child Psychotherapy (TF-CBT TPOCS-S), a behaviorally specific checklist of TF-CBT provider behavior that we have modified for the current study to ensure relevance to the eTF-CBT condition. This checklist will be used to calculate providers' fidelity to each TF-CBT component. Two independent raters will listen to video-recorded treatment session tapes and complete the TF-CBT TPOCS-S to code the presence/absence of specific treatment techniques depicted on the tapes.

Secondary Outcome Measures

  1. Center for Epidemiological Studies Depression Scale for Children (CES-DC) [baseline, 3, 6, 9, 12 months post baseline]

    assesses the severity of depressive symptomatology in children. It is a 20-item self-report measure with possible scores ranging from 0-60. Scores over 15 are indicative of significant levels of depressive symptoms.

  2. Therapeutic Alliance Scale for Children (TASC) [baseline, 3, 6, 9, 12 months post baseline]

    The TASC is an 8-item measure of the child's alliance with the therapist using a 4-pt scale. It has good internal consistency and interrater reliability.

  3. Child/Adolescent Satisfaction Questionnaire (CASQ). [baseline, 3, 6, 9, 12 months post baseline]

    The CASQ is a 15-item instrument that assesses child satisfaction with mental health treatment.

  4. The Shame Measure [baseline, 3, 6, 9, 12 months post baseline]

    4-item instrument that assesses feelings of shame following abuse.

  5. The Child and Adolescent Trauma Screen (CATS) - Youth Version [baseline, 3, 6, 9, 12 months post baseline]

    35-item instrument that assesses exposure to traumatic events and all 20 DSM-V symptoms of PTSD.

  6. Caregiver Satisfaction Questionnaire (CSQ) [baseline, 3, 6, 9, 12 months post baseline]

    The CSQ is a 15-item instrument that assesses caregiver satisfaction with mental health treatment.

  7. Working Alliance Inventory (WAI-short form) [baseline, 3, 6, 9, 12 months post baseline]

    The WAI is a 12-item measure of the parent-therapist alliance using a 7-point scale (never to always).

  8. Brief Problems Monitor (BPM) [baseline, 3, 6, 9, 12 months post baseline]

    The BPM is a 19-item measure of emotional and behavioral functioning in children. The BPM is well-validated and comparable to the lengthier Child Behavior Checklist.

  9. Center for Epidemiologic Studies Depression Scale (CESD-R). [baseline, 3, 6, 9, 12 months post baseline]

    The CESD-R is a 20-item self-report scale of depression. It is widely used and demonstrates excellent psychometric properties.

  10. The Child and Adolescent Trauma Screen (CATS) - Caregiver Version [baseline, 3, 6, 9, 12 months post baseline]

    35-item parent version of the CATS-Youth.

  11. The Alabama Parenting Questionnaire [baseline, 3, 6, 9, 12 months post baseline]

    42-item measure to assess parenting practices.

  12. The Kessler 6 [baseline, 3, 6, 9, 12 months post baseline]

    widely used 6-item measure of general distress that is well-validated.

  13. Evidence-Based Practice Attitude Scale (EBPAS) [baseline, post baseline]

    15 items, assessing providers' perceptions of appeal of EBT, openness to innovation, perceived divergence with usual care (alphas .59-.90; M=.77).

  14. Knowledge of Behavioral Principles as Applied to Children [baseline, post baseline]

    assess understanding of the application of behavioral principles to youth. Internal consistency=.42-.84; sensitivity to change.

  15. Acceptability, Appropriateness and Feasibility Measure ( [baseline, post baseline]

    12-item measure to monitor and evaluate implementation efforts. This measure has been shown to have solid psychometric properties.

  16. Computer Assisted Therapy Attitudes Scale [baseline, post baseline]

    8-item measure design to assess attitudes toward computer use in treatment.

  17. Organizational Readiness for Implementing Change [baseline, post baseline]

    12-item measure designed to assess an organization's readiness to implement new policies, programs, and practices.

  18. TF-CBT Organizational Support Measure [baseline, post baseline]

    19-item instrument to assess a community mental health organization's activities related to the delivery of Trauma-Focused Cognitive-Behavioral Therapy (TF-CBT).

  19. Burnout Measure [baseline, post baseline]

    screener that assesses providers' feelings about their work, and their perceptions of how their co-workers feel about the work they do.

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • victim of at least one potentially traumatic event (e.g. sexual/physical assault, witnessed violence, disaster, serious accident)

  • have at least one symptom on each PTSD symptom cluster (re-experiencing, avoidance, hyperarousal)

Exclusion Criteria:
  • exhibits psychotic symptoms (active hallucinations, delusions, impaired thought processes) by caregiver or child

  • significant cognitive disabilities, developmental delays, or pervasive developmental disorder

  • active suicidal or homicidal ideations

  • no consistent caregiver available to participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of South Carolina Charleston South Carolina United States 29425

Sponsors and Collaborators

  • Medical University of South Carolina

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT03305458
Other Study ID Numbers:
  • R01MH110620
First Posted:
Oct 10, 2017
Last Update Posted:
Sep 9, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 9, 2021