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Setting Families on a Positive Path to Recovery After Pediatric TBI: Road-to-Recovery

Primary Purpose

Traumatic Brain Injury, Head Injury, Head Injuries, Closed

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Road-to-recovery
Sponsored by
Children's Hospital Medical Center, Cincinnati
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Caregivers will be eligible if they are over 18 years of age, and if their child meets all of the following criteria: Ages 3 months to 18 years at time of discharge from hospital Sustained a complicated mild to severe TBI as defined by a Glasgow Coma Scale (GCS) of 13-15 with imagining abnormalities or GCS 3-12 with or without imaging abnormalities Admitted overnight to the hospital 0-3 months post-discharge Exclusion Criteria: The caregiver will be excluded from participation if any of the following occur: Child did not survive the injury Child sustained a non-blunt head trauma (e.g. gunshot wound) Child does not reside with parent/caregiver for study duration English is not primary language spoken in the home

Sites / Locations

  • Cincinnati Children's Hospital Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Road-to-recovery group (R2R)

Internet resources comparison group (IRC)

Arm Description

Usual medical care plus the R2R-TBI intervention (self-guided web-program)

Usual medical care plus internet resources

Outcomes

Primary Outcome Measures

Parent anxiety
Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Measure 4a; scores range from 4-20 with higher score indicating greater symptoms of anxiety
Parent anxiety
Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Measure 4a; scores range from 4-20 with higher score indicating greater symptoms of anxiety
Parent depression
Center for Epidemiological Studies Depression Scale (CES-D; 10-items); scores range from 0 -30 with higher scores indicating of higher levels of depressive symptomatology
Parent depression
Center for Epidemiological Studies Depression Scale (CES-D; 10-items); scores range from 0 -30 with higher scores indicating of higher levels of depressive symptomatology
Parenting self-efficacy
Caregiver self-efficacy scale (CSES); scores range from 25-100, higher scores indicate greater parenting self efficacy
Parenting self-efficacy
Caregiver self-efficacy scale (CSES); scores range from 25-100, higher scores indicate greater parenting self efficacy
Parent post-traumatic symptoms
Primary Care PTSD Screen for DSM-5 (PC-PTSD-5); scores rage from 0-5 with higher scores indicating greater experience of post-traumatic stress symptoms
Parent post-traumatic symptoms
Primary Care PTSD Screen for DSM-5 (PC-PTSD-5); scores rage from 0-5 with higher scores indicating greater experience of post-traumatic stress symptoms

Secondary Outcome Measures

Family Functioning
Family Assessment Device - Global Functioning Scale. Scores range from 1 to 4 with higher scores indicating poorer family functioning
Family Functioning
Family Assessment Device - Global Functioning Scale. Scores range from 1 to 4 with higher scores indicating poorer family functioning
Family Burden of Injury
Family Burden of Injury Interview (FBII). Average scores range from 0-4; higher scores indicate greater injury-related burden
Family Burden of Injury
Family Burden of Injury Interview (FBII). Average scores range from 0-4; higher scores indicate greater injury-related burden
Child Socioemotional Functioning
Pediatric Quality of Life Scale (PEDS-QL) - Psychosocial Health Summary Score (score range varies based on child age; higher scores indicate greater health related quality of life)
Child Socioemotional Functioning
Pediatric Quality of Life Scale (PEDS-QL) - Psychosocial Health Summary Score (score range varies based on child age; higher scores indicate greater health related quality of life)
Parent mindful self-care
Mindful self-care scale (MSCS); scores range from 6 - 30, higher scores denote greater frequency in engaging in self-care behaviors
Parent mindful self-care
Mindful self-care scale (MSCS); scores range from 6 - 30, higher scores denote greater frequency in engaging in self-care behaviors
Parent resilience
Connor-Davidson Resilience Scale (CDRI); scores range from 0-40 with higher scored indicating greater resilience
Parent resilience
Connor-Davidson Resilience Scale (CDRI); scores range from 0-40 with higher scored indicating greater resilience

Full Information

First Posted
October 24, 2022
Last Updated
May 31, 2023
Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Nationwide Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05622461
Brief Title
Setting Families on a Positive Path to Recovery After Pediatric TBI: Road-to-Recovery
Official Title
Setting Families on a Positive Path to Recovery After Pediatric TBI: Road-to-Recovery, A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 13, 2023 (Actual)
Primary Completion Date
July 30, 2024 (Anticipated)
Study Completion Date
October 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Nationwide Children's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study has two main goals: 1) to refine and enhance the R2R-TBI intervention; and 2) to examine the efficacy of the R2R-TBI intervention in a randomized control trial. To achieve the second goal, we will employ a between-groups randomized treatment design with repeated measures at baseline, one-month post-randomization, and at a six-month follow-up. The two conditions will be: a) usual medical care plus access to internet resources regarding pediatric brain injury (Internet Resources Comparison group, IRC), and b) usual medical care plus the R2R-TBI intervention (Road-to-Recovery group, R2R-TBI).
Detailed Description
The early recovery period constitutes a critical window to set families on a positive road-to-recovery by supporting parental self-care, positive parent-child interactions, and awareness of potential longer-term concerns. The latter would facilitate parental recognition of behavioral and psychosocial needs that might otherwise go unmet. Recognizing that (1) caregivers of children who have sustained TBI are at risk of worsening psychological health and that (2) caregiver functioning and parenting behaviors have a direct impact on child recovery and outcomes; intervening and supporting caregivers in the acute phase following injury may set children and families on a positive path to recovery. Intervening at the acute phase may reduce the cascading effects of parental burden/distress and concomitant negative parent-child interactions on child recovery and functioning over time. Because families of children with TBI and other chronic health conditions may have difficulty accessing services due to transportation and cost issues, particularly lower income families, the R2R-TBI program is designed to be accessed via any web-enabled device (e.g., smartphone, computer, tablet) with any form of internet connection. We will also offer the intervention (via tablet) to parents while they wait for their child to complete outpatient therapies (e.g., speech, physical, and occupational therapy). Delivery of web-based behavioral health interventions may reduce barriers to help-seeking and promote evidence-based interventions that are both accessible and efficient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury, Head Injury, Head Injuries, Closed, Brain Hemorrhage, Traumatic, Brain Edema, Intracranial Edema

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Road-to-recovery group (R2R)
Arm Type
Experimental
Arm Description
Usual medical care plus the R2R-TBI intervention (self-guided web-program)
Arm Title
Internet resources comparison group (IRC)
Arm Type
Active Comparator
Arm Description
Usual medical care plus internet resources
Intervention Type
Behavioral
Intervention Name(s)
Road-to-recovery
Intervention Description
R2R-TBI is a self-guided web-based intervention that targets caregiver psychological functioning, parenting behaviors, and family functioning in the first three months following pediatric traumatic brain injury.
Primary Outcome Measure Information:
Title
Parent anxiety
Description
Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Measure 4a; scores range from 4-20 with higher score indicating greater symptoms of anxiety
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Parent anxiety
Description
Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Measure 4a; scores range from 4-20 with higher score indicating greater symptoms of anxiety
Time Frame
Change from baseline at 6 months
Title
Parent depression
Description
Center for Epidemiological Studies Depression Scale (CES-D; 10-items); scores range from 0 -30 with higher scores indicating of higher levels of depressive symptomatology
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Parent depression
Description
Center for Epidemiological Studies Depression Scale (CES-D; 10-items); scores range from 0 -30 with higher scores indicating of higher levels of depressive symptomatology
Time Frame
Change from baseline at 6 months
Title
Parenting self-efficacy
Description
Caregiver self-efficacy scale (CSES); scores range from 25-100, higher scores indicate greater parenting self efficacy
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Parenting self-efficacy
Description
Caregiver self-efficacy scale (CSES); scores range from 25-100, higher scores indicate greater parenting self efficacy
Time Frame
Change from baseline at 6 months
Title
Parent post-traumatic symptoms
Description
Primary Care PTSD Screen for DSM-5 (PC-PTSD-5); scores rage from 0-5 with higher scores indicating greater experience of post-traumatic stress symptoms
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Parent post-traumatic symptoms
Description
Primary Care PTSD Screen for DSM-5 (PC-PTSD-5); scores rage from 0-5 with higher scores indicating greater experience of post-traumatic stress symptoms
Time Frame
Change from baseline at 6 months
Secondary Outcome Measure Information:
Title
Family Functioning
Description
Family Assessment Device - Global Functioning Scale. Scores range from 1 to 4 with higher scores indicating poorer family functioning
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Family Functioning
Description
Family Assessment Device - Global Functioning Scale. Scores range from 1 to 4 with higher scores indicating poorer family functioning
Time Frame
Change from baseline at 6 months
Title
Family Burden of Injury
Description
Family Burden of Injury Interview (FBII). Average scores range from 0-4; higher scores indicate greater injury-related burden
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Family Burden of Injury
Description
Family Burden of Injury Interview (FBII). Average scores range from 0-4; higher scores indicate greater injury-related burden
Time Frame
Change from baseline at 6 months
Title
Child Socioemotional Functioning
Description
Pediatric Quality of Life Scale (PEDS-QL) - Psychosocial Health Summary Score (score range varies based on child age; higher scores indicate greater health related quality of life)
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Child Socioemotional Functioning
Description
Pediatric Quality of Life Scale (PEDS-QL) - Psychosocial Health Summary Score (score range varies based on child age; higher scores indicate greater health related quality of life)
Time Frame
Change from baseline at 6 months
Title
Parent mindful self-care
Description
Mindful self-care scale (MSCS); scores range from 6 - 30, higher scores denote greater frequency in engaging in self-care behaviors
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Parent mindful self-care
Description
Mindful self-care scale (MSCS); scores range from 6 - 30, higher scores denote greater frequency in engaging in self-care behaviors
Time Frame
Change from baseline at 6 months
Title
Parent resilience
Description
Connor-Davidson Resilience Scale (CDRI); scores range from 0-40 with higher scored indicating greater resilience
Time Frame
Change from baseline at 4-6 weeks post-intervention
Title
Parent resilience
Description
Connor-Davidson Resilience Scale (CDRI); scores range from 0-40 with higher scored indicating greater resilience
Time Frame
Change from baseline at 6 months
Other Pre-specified Outcome Measures:
Title
Moderators of treatment effects
Description
Examining household income and baseline caregiver distress as moderator of treatment effects
Time Frame
4-6 weeks
Title
Moderators of treatment effects
Description
Examining household income and baseline caregiver distress as moderator of treatment effects
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Caregivers will be eligible if they are over 18 years of age, and if their child meets all of the following criteria: Ages 3 months to 18 years at time of discharge from hospital Sustained a complicated mild to severe TBI as defined by a Glasgow Coma Scale (GCS) of 13-15 with imagining abnormalities or GCS 3-12 with or without imaging abnormalities Admitted overnight to the hospital 0-3 months post-discharge Exclusion Criteria: The caregiver will be excluded from participation if any of the following occur: Child did not survive the injury Child sustained a non-blunt head trauma (e.g. gunshot wound) Child does not reside with parent/caregiver for study duration English is not primary language spoken in the home
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shari Wade, PhD
Phone
5134610952
Email
Shari.Wade@cchmc.org
First Name & Middle Initial & Last Name or Official Title & Degree
Stacey Raj
Email
rajs@xavier.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shari Wade, PhD
Organizational Affiliation
CCHMC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229-3036
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shari Wade
Phone
513-461-0952
Email
Shari.Wade@cchmc.org
First Name & Middle Initial & Last Name & Degree
Stacey Raj
Email
rajs@xavier.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Plan is to share deidentified data as consistent with requirement of funding source (i.e., The National Institute on Disability and Rehabilitation Research).
IPD Sharing Time Frame
Starting 6 months after publication
IPD Sharing Access Criteria
Plan is to share deidentified data as consistent with protocols of funding source (i.e., The National Institute on Disability and Rehabilitation Research).

Learn more about this trial

Setting Families on a Positive Path to Recovery After Pediatric TBI: Road-to-Recovery

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