MedPath

Optimizing Residential Treatment Gains for Adolescents

Not Applicable
Active, not recruiting
Conditions
Adolescent - Emotional Problem
Parenting
Mental Disorder in Adolescence
Interventions
Behavioral: TAU
Behavioral: Parenting Wisely Residential Treatment (PWRT)
Registration Number
NCT05764369
Lead Sponsor
Ohio State University
Brief Summary

The goal of this randomized controlled trial is to determine the feasibility, acceptability, and preliminary effects of a web-based parent training (Parenting Wisely) augmented with facilitated parent groups (referred to as PWRT). PWRT is designed to prepare parents for the reintegration of their adolescents in the home after intensive psychiatric residential treatment. Researchers will compare PWRT to treatment as usual to determine whether PWRT effects target mechanisms (i.e., family function, social support, parental self-efficacy, parenting practices) and adolescent outcomes (i.e., internalizing and externalizing behaviors, placement restrictiveness).

Detailed Description

A randomized controlled trial (RCT) design is employed to evaluate the feasibility, acceptability, engagement of target mechanisms, and preliminary effects of PWRT in parents with adolescents transitioning from residential treatment (RT) to the community. Parents (n=60) will be randomly assigned to receive Parenting Wisely augmented with facilitated discussion groups (referred to as PWRT; n=30) or treatment-as-usual (TAU; n=30). In the PWRT condition, parents will complete 2 web-based modules in an online parent training program called Parenting Wisely. Parents will also attend a 90-minute discussion group via Zoom. The RCT will allow for testing of target mechanism engagement (i.e., parental self-efficacy, parenting behaviors, social support, family function) and the intervention's effects on adolescent outcomes (i.e., internalizing behaviors, externalizing behaviors, placement restrictiveness). Parents will complete assessments at baseline (T1), six weeks post-baseline (T2), and six months post-baseline (T3) via REDCap. While adolescents (n=60) will not directly receive the intervention, they will complete assessments at baseline, six weeks post-baseline (T2), and six months post-baseline (T3).

Aim 1: Evaluate the feasibility and acceptability of PWRT. 1a. Evaluate the feasibility of PWRT by tracking the frequency, dose, and duration. 1b. Evaluate the acceptability of PWRT for parents with adolescents in RT.

Aim 2: Determine the effects of PWRT on the target mechanisms compared to the TAU condition from baseline to 6-weeks and 6-months post-baseline.

Aim 3: Determine the effects of PWRT on adolescent outcomes compared to the TAU condition from baseline to 6-weeks and 6-months post-baseline. 3a. Determine if changes in the target mechanisms are associated with adolescent outcomes at six weeks and six months post-baseline.

Exploratory Aim: Explore the feasibility of collecting data from adolescents in an RT facility by tracking frequency (recruitment, enrollment, retention rates), duration (time between parent consent and assent; survey duration), and barriers to data collection.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Caregiver (e.g., biological, step, kin, foster, adoptive) to an adolescent aged 11-17 years old who is admitted to psychiatric residential treatment;
  • The caregiver is allowed contact with the adolescent;
  • Has access to a device (e.g., smartphone) with internet access.

Adolescent Inclusion Criteria:

  • Ability to understand and willingness to provide written assent
  • Legal guardian provides written consent;
  • Currently or previously admitted to psychiatric residential treatment
  • Aged 11-17 years at enrollment;

Parent and Adolescent

Exclusion Criteria
  • Not able to speak English

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Treatment as Usual (TAU)TAUThe TAU condition is the standard of care offered to parents in RT settings. Parents in the TAU condition will receive traditional programming, including family therapy offered weekly during the RT admission. Parents will attend discharge planning meetings with caseworkers (if assigned) to discuss the adolescent's progress, continued treatment needs, safety plans, upcoming appointments, and medication needs. Following discharge, programs frequently recommend follow-up with an outpatient provider for medication management and therapy for the adolescent. Parents will complete assessments at baseline (T1), six weeks post-baseline (T2), and six months post-baseline (T3) via REDCap. While adolescents (n=60) will not directly receive the intervention, they will complete assessments at baseline, six weeks post-baseline (T2), and six months post-baseline (T3).
Parenting Wisely Residential Treatment (PWRT)Parenting Wisely Residential Treatment (PWRT)In the PWRT condition, parents will complete a total of ten web-based modules in an online parent training program called Parenting Wisely. Each week, parents will also attend a 90-minute facilitated discussion group via Zoom. Parents will complete assessments at baseline (T1), six weeks post-baseline (T2), and six months post-baseline (T3) via REDCap. While adolescents (n=60) will not directly receive the intervention, they will complete assessments at baseline, six weeks post-baseline (T2), and six months post-baseline (T3).
Primary Outcome Measures
NameTimeMethod
Dose of PWRT (Feasibility)Average calculated from baseline to 6-weeks post-baseline

The number of modules in Parenting Wisely that are completed are tracked and an average completion rate across all sessions will be calculated

Duration of group (Feasibility)Average calculated from baseline to 6-weeks post-baseline

The time spent in group is tracked and an average duration rate across all sessions will be calculated

PWRT Acceptability6-weeks post-baseline

Parents will complete an investigator-developed satisfaction survey to evaluate the acceptability of PWRT. The satisfaction survey consists of 13-items. Total scores range from 0-39; higher scores indicate greater perceptions of acceptability.

Group attendance frequency (Feasibility)Average calculated from baseline to 6-weeks post-baseline

Group attendance is tracked and an average attendance rate across all sessions will be calculated

Parenting Wisely login frequency (Feasibility)Average calculated from baseline to 6-weeks post-baseline

The number of logins to Parenting Wisely is tracked and an average logins across all sessions will be calculated

Duration of PW modules (Feasibility)Average calculated from baseline to 6-weeks post-baseline

The time spent completing modules in Parenting Wisely are tracked and an average duration rate across all sessions will be calculated

Secondary Outcome Measures
NameTimeMethod
Change in Parenting PracticesChange from baseline to 6-months post-baseline

The Adult-Adolescent Parenting Inventory (AAPI) will be administered to parents to evaluate changes in parenting practices. The AAPI consists of 40-items and is designed for parents of adolescents aged 12 to 17. The AAPI assesses parenting and rearing attitudes and practices. Total scores range from 40-200; higher scores indicate more effective parenting practices.

Change in Adolescent Internalizing BehaviorsChange from baseline to 6-weeks post-baseline

Adolescent internalizing behaviors will be assessed using the Brief Problem Monitor (BPM) for ages 6 to 18. The BPM consists of 19 items derived from the Child Behavior Checklist. The subscales include internalizing, externalizing, and attention subscales. Raw scores range from 0-38; higher scores indicate greater internalizing behaviors.

Change in Family FunctionChange from baseline to 6-months post-baseline

The McMaster Family Assessment Device (FAD) will be administered to parents to evaluate changes in family function. The FAD consists of 60-items that assess seven domains of family function: problem-solving, family roles, communication, affective involvement, affective responsiveness, behavioral control, general functioning. Total scores range from 60-240; higher scores indicate better family function.

Change in Social SupportChange from baseline to 6-months post-baseline

The Medical Outcomes Study (MOS) Social Support Survey will be administered to parents to evaluate changes in social support. The MOS consists of 19-items that assess five social support domains: emotional support, informational support, tangible support, affectionate support, and positive social interaction.Total scores range from 20-100; higher scores indicate greater social support.

Change in Adolescent Externalizing BehaviorsChange from baseline to 6-months post-baseline

Adolescent externalizing behaviors will be assessed using the Brief Problem Monitor (BPM) for ages 6 to 18. The BPM consists of 19 items derived from the Child Behavior Checklist. The subscales include internalizing, externalizing, and attention subscales. Raw scores range from 0-38; higher scores indicate greater externalizing behaviors.

Change in Restrictiveness of Living EnvironmentChange from baseline to 6-months post-baseline

The Restrictiveness Evaluation Measure (REM) will be administered to parents and adolescents to evaluate perceptions of adolescent placement restrictiveness. The REM was designed and tested in residential treatment settings. There are two subscales; one scale identifies 25 placement settings varying in restrictiveness and the second subscale consists of questions about the activity and lifestyle restrictions in such placements. Total scores range from 24-120; higher scores indicate more restrictive living environments.

Change in Parenting Self EfficacyChange from baseline to 6-months post-baseline

Parents will complete the Parenting Sense of Competence Scale (PSOC) to evaluate changes in parental self-efficacy. The PSOC consists of 17-items and is designed for parents with children aged birth to 17. The two subscales in the PSOC are satisfaction and efficacy. Total scores range from 17-102; higher scores indicate greater perceptions of self-efficacy and confidence.

Trial Locations

Locations (1)

Ohio State University College of Nursing

🇺🇸

Columbus, Ohio, United States

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