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Character Strengths Intervention Among Psychiatrically Hospitalized Youth

Primary Purpose

Psychiatric Hospitalization, Mental Disorders, Child/Adolescent Problems

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Identifying and Using Signature Strengths
Identifying and Writing Down Coping Skills
Treatment as Usual
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Psychiatric Hospitalization

Eligibility Criteria

12 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient on Child and Adolescent Psychiatric Unit

Exclusion Criteria:

  • Cognitive disability or severe psychosis preventing understanding of survey measures
  • Prior use of VIA-Youth Survey
  • Absence of legal guardian to consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Active Comparator

    Other

    Arm Label

    Signature Strengths

    Coping Skills + Memory Aid

    Coping Skills (Treatment as Usual)

    Arm Description

    Patients will complete the Values in Action Youth Survey (VIA-Youth) and will receive a list of his/her top character strengths ("signature strengths"). The patient will then participate in the Identifying and Using Signature Strengths Intervention.

    Patients will complete the VIA-Youth but will not receive any results. The patient will then participate in the Identifying and Writing Down Coping Skills Intervention.

    Patients will complete the VIA-Youth but will not receive any results. After completing the VIA-Youth, the study team member and patient will have a treatment-as-usual discussion about coping skills. (This is equivalent to treatment as usual that is already provided on the psychiatric unit-doctors and nurses on the unit already have this a discussion about coping skills with patients).

    Outcomes

    Primary Outcome Measures

    Change in depression symptoms over time compared to baseline
    Depression will be measured using Patient Health Questionnaire (PHQ) for adolescents, and percent change in depression score will be compared across the 3 arms.
    Change in anxiety symptoms over time compared to baseline
    Anxiety will be measured using the 5-item Screen for Child Anxiety Related Emotional Disorders (SCARED), and percent change in anxiety score will be compared across the 3 arms.

    Secondary Outcome Measures

    Change in self-esteem over time compared to baseline
    Self-esteem will be measured using the Rosenberg Self-Esteem Scale (SES), and percent change in self-esteem score will be compared across the 3 arms.
    Change in self-efficacy over time compared to baseline
    Self-efficacy will be measured using the General Self-Efficacy Scale (GSE), and percent change in self-efficacy score will be compared across the 3 arms.
    Change in resiliency over time compared to baseline
    Resiliency will be measured using the 10-item Connor Davidson Resiliency Scale (CD-RISC-10), and percent change in resiliency score will be compared across the 3 arms.
    Change in life-satisfaction over time compared to baseline
    Life satisfaction will be measured using the Brief Multidimensional Students' Life Satisfaction Scale - PTPB version (BMSLSS-PTPB), and percent change in life satisfaction score will be compared across the 3 arms.

    Full Information

    First Posted
    January 29, 2016
    Last Updated
    August 30, 2019
    Sponsor
    University of Michigan
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02674932
    Brief Title
    Character Strengths Intervention Among Psychiatrically Hospitalized Youth
    Official Title
    Assessment of a Character Strengths Intervention in Improving Treatment Outcomes Among Psychiatrically Hospitalized Youth
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2016 (Actual)
    Primary Completion Date
    December 2017 (Actual)
    Study Completion Date
    December 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Michigan

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Research has shown that identifying and using one's character strengths in new ways decreases depressive symptoms and increases happiness in adults in the general population. Recently, we found that a similar intervention increases the self-esteem and self-efficacy of children and adolescents being treated in an inpatient psychiatric unit. The purpose of this study is to better understand the effects that discovering one's character strengths and incorporating them into coping skills will have on treatment outcomes in patients admitted to a child and adolescent inpatient psychiatric unit.
    Detailed Description
    The primary aim of this study is to investigate whether a character strengths-based intervention results in significant improvements in measures of depression, anxiety, resiliency, optimism, self-perception, and life-satisfaction of psychiatrically hospitalized youth up to three months following admission. Secondary aims are to: (1) examine participants' strengths profile to identify potential correlates between character strengths, psychiatric diagnoses and intervention effectiveness; and (2) determine whether patients who continue to incorporate their strengths into coping skills at follow-up assessments exhibit greater improvement over-time. Participants will be 210 adolescents aged 12 to 17 years admitted to the Child and Adolescent Psychiatric Inpatient Program and will be randomized into one of the three groups. All participants will complete the Values in Action Inventory of Strengths for Youth (VIA-Youth) Survey on their second hospital day and subsequently receive the signature strengths intervention (experimental group), coping skills with memory aids comparison exercise (positive control group), or coping skills without memory aids (treatment-as-usual control group). Outcome measures will be completed by all participants at baseline (day 1 on unit), post-treatment (day 4 on unit), and 1- and 3-months following admission. The proposed research represents a change in paradigm, as we aim to specifically examine the therapeutic benefit of the positive psychology element of our intervention conducted in the pilot study among youth with severe mental illness.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Psychiatric Hospitalization, Mental Disorders, Child/Adolescent Problems

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    153 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Signature Strengths
    Arm Type
    Experimental
    Arm Description
    Patients will complete the Values in Action Youth Survey (VIA-Youth) and will receive a list of his/her top character strengths ("signature strengths"). The patient will then participate in the Identifying and Using Signature Strengths Intervention.
    Arm Title
    Coping Skills + Memory Aid
    Arm Type
    Active Comparator
    Arm Description
    Patients will complete the VIA-Youth but will not receive any results. The patient will then participate in the Identifying and Writing Down Coping Skills Intervention.
    Arm Title
    Coping Skills (Treatment as Usual)
    Arm Type
    Other
    Arm Description
    Patients will complete the VIA-Youth but will not receive any results. After completing the VIA-Youth, the study team member and patient will have a treatment-as-usual discussion about coping skills. (This is equivalent to treatment as usual that is already provided on the psychiatric unit-doctors and nurses on the unit already have this a discussion about coping skills with patients).
    Intervention Type
    Behavioral
    Intervention Name(s)
    Identifying and Using Signature Strengths
    Intervention Description
    The purpose of the intervention is to identify and focus on one's morally valued strengths and utilize them (i.e. incorporate them into coping skills) to overcome challenges. The study team member and patient will discuss each top strength and ways to use them as coping skills. The patient will identify 2-4 coping mechanisms per strength, and will write his/her strengths and self-identified coping skills on index cards.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Identifying and Writing Down Coping Skills
    Intervention Description
    The study team member and patient will discuss the importance of having coping skills to deal with stressful and difficult situations. The patient will then identify at least six coping skills and write them down on index cards.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Treatment as Usual
    Intervention Description
    The study team member and patient will discuss the importance of having coping skills to deal with stressful and difficult situations. The patient will then identify coping skills that could be helpful (but will not write them down).
    Primary Outcome Measure Information:
    Title
    Change in depression symptoms over time compared to baseline
    Description
    Depression will be measured using Patient Health Questionnaire (PHQ) for adolescents, and percent change in depression score will be compared across the 3 arms.
    Time Frame
    baseline, 3 days, 1 month, 3 months
    Title
    Change in anxiety symptoms over time compared to baseline
    Description
    Anxiety will be measured using the 5-item Screen for Child Anxiety Related Emotional Disorders (SCARED), and percent change in anxiety score will be compared across the 3 arms.
    Time Frame
    baseline, 3 days, 1 month, 3 months
    Secondary Outcome Measure Information:
    Title
    Change in self-esteem over time compared to baseline
    Description
    Self-esteem will be measured using the Rosenberg Self-Esteem Scale (SES), and percent change in self-esteem score will be compared across the 3 arms.
    Time Frame
    baseline, 3 days, 1 month, 3 months
    Title
    Change in self-efficacy over time compared to baseline
    Description
    Self-efficacy will be measured using the General Self-Efficacy Scale (GSE), and percent change in self-efficacy score will be compared across the 3 arms.
    Time Frame
    baseline, 3 days, 1 month, 3 months
    Title
    Change in resiliency over time compared to baseline
    Description
    Resiliency will be measured using the 10-item Connor Davidson Resiliency Scale (CD-RISC-10), and percent change in resiliency score will be compared across the 3 arms.
    Time Frame
    baseline, 3 days, 1 month, 3 months
    Title
    Change in life-satisfaction over time compared to baseline
    Description
    Life satisfaction will be measured using the Brief Multidimensional Students' Life Satisfaction Scale - PTPB version (BMSLSS-PTPB), and percent change in life satisfaction score will be compared across the 3 arms.
    Time Frame
    baseline, 3 days, 1 month, 3 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    12 Years
    Maximum Age & Unit of Time
    17 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patient on Child and Adolescent Psychiatric Unit Exclusion Criteria: Cognitive disability or severe psychosis preventing understanding of survey measures Prior use of VIA-Youth Survey Absence of legal guardian to consent
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Paresh D Patel, MD, PhD
    Organizational Affiliation
    Department of Psychiatry, University of Michigan
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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