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Engaging Parents in Neuropsychological Rehabilitation for Childhood Cancer Survivors: The ImPACT Program - A Pilot Study

Primary Purpose

Pediatric Cancer, Cognitive Dysfunction

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
ImPACT
Sponsored by
Aarhus University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pediatric Cancer focused on measuring Pediatric Cancer, Cognitive Dysfunction, Neuropsychological Rehabilitation, Neurobehavioral Impairment

Eligibility Criteria

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

Inclusion Criteria:

  • Cancer diagnosis of a leukemia, lymphoma, or central nervous system tumor
  • Completed primary treatment at least 6 months ago
  • Not terminally ill
  • Attend school
  • Living with one or more parents who speak Danish and are willing to co-participate
  • Screened as having parent-reported clinically significant cognitive and/or neurobehavioral impairment

Exclusion Criteria:

• Confounding diagnosed or suspected psychiatric or medical condition unrelated to the cancer or its treatment that might contribute to cognitive or neurobehavioral impairment

Sites / Locations

  • Aarhus UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ImPACT program

Arm Description

The ImPACT program consists of 8 weekly 1-hour sessions with homework between sessions.

Outcomes

Primary Outcome Measures

Parent-reported neurobehavioral functioning
The parent-report screening version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 12 items: answer format range: 1-3; total score range: 12-36. Higher score indicates more impairment.
Parent-reported cognitive functioning
The parent-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.

Secondary Outcome Measures

Parent-reported neurobehavioral functioning
The parent-report version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 63 items: answer format range: 1-3; total score range: 63-189. Higher score indicates more impairment.
Parent-reported cognitive functioning
The parent-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Child-reported neurobehavioral functioning
The child-report version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 55 items: answer format range: 1-3; total score range: 55-165. Higher score indicates more impairment.
Child-reported neurobehavioral functioning
The child-report version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 55 items: answer format range: 1-3; total score range: 55-165. Higher score indicates more impairment.
Child-reported cognitive functioning
The child-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Child-reported cognitive functioning
The child-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Parent-reported pediatric quality of life
The parent-report version of the Pediatric Quality of Life (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate more impairment.
Parent-reported pediatric quality of life
The parent-report version of the Pediatric Quality of Life Inventory (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate lower quality of life.
Child-reported pediatric quality of life
The child-report version of the Pediatric Quality of Life (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate more impairment.
Child-reported pediatric quality of life
The child-report version of the Pediatric Quality of Life (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate more impairment.
Parent-reported pediatric anxiety and depression
The parent-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Parent-reported pediatric anxiety and depression
The parent-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Child-reported pediatric anxiety and depression
The child-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Child-reported pediatric anxiety and depression
The child-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Parent-reported pediatric fatigue
The parent-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Parent-reported pediatric fatigue
The parent-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Child-reported pediatric fatigue
The child-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Child-reported pediatric fatigue
The child-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Parent sense of competence
The Parenting Sense of Competence Scale (PSC scale).17 items: answer format range 1-6; total score range: 16-102. Higher score indicates more competence.
Parent sense of competence
The Parenting Sense of Competence Scale (PSC scale). 17 items: answer format range 1-6; total score range: 16-102. Higher score indicates more competence.
Parent-reported participant motivation
The 7-item interest/enjoyment subscale of the Intrinsic Motivation Inventory (IMI). 7 items: answer format range 1-7; total score range: 1-7. Higher score indicates more motivation.
Child-reported participant motivation
The 7-item interest/enjoyment subscale of the Intrinsic Motivation Inventory (IMI). 7 items: answer format range 1-7; total score range: 1-7. Higher score indicates more motivation.
Parent-reported participant satisfaction
The Client Satisfaction Questionnaire (CSQ-8). 8 items: answer format range 1-4; total score range: 8-32. Higher score indicates better satisfaction.
Child-reported participant satisfaction
The Client Satisfaction Questionnaire (CSQ-8). 8 items: answer format range 1-4; total score range: 8-32. Higher score indicates better satisfaction.
Objective cognitive functioning (Child only)
Standard neuropsychological test battery. Different scoring formats.
Objective cognitive functioning (Child only)
Standard neuropsychological test battery. Different scoring formats.

Full Information

First Posted
July 19, 2022
Last Updated
November 21, 2022
Sponsor
Aarhus University Hospital
Collaborators
University of Aarhus
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1. Study Identification

Unique Protocol Identification Number
NCT05483166
Brief Title
Engaging Parents in Neuropsychological Rehabilitation for Childhood Cancer Survivors: The ImPACT Program - A Pilot Study
Official Title
Engaging Parents in Neuropsychological Rehabilitation for Childhood Cancer Survivors: The "I'm Aware: Parents and Children Together" (ImPACT) Program - A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2022 (Actual)
Primary Completion Date
October 1, 2023 (Anticipated)
Study Completion Date
October 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aarhus University Hospital
Collaborators
University of Aarhus

4. Oversight

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

5. Study Description

Brief Summary
The aim of the present pilot study is to evaluate the feasibility, acceptability, and preliminary efficacy of a novel, context-sensitive neuropsychological rehabilitation intervention for childhood cancer survivors and their families.
Detailed Description
Cognitive impairment is the most common late effect in childhood cancer survivors, and despite the negative effects of these symptoms on quality of life, scholastic achievement and long-term socioeconomic outcomes, there continues to be no "gold standard" treatment for childhood cancer survivors with cognitive impairment. Indeed, there is a dearth of research on interventions to treat cognitive impairment in childhood cancer survivors, and the relatively few studied interventions have proven limited effects. Arguably, four key elements are missing from a majority of studied interventions:1) transfer of learning to real-world functional outcomes, 2) awareness training to enhance compensatory strategy use, 3) inclusion of parents that could enhance transfer of learning to the home, and 4) recognition of the inter-related nature of cognitive, neurobehavioral, and psychological functions. The "I'M aware: Parents and Children Together (ImPACT)" program is a novel, context-sensitive neuropsychological rehabilitation intervention that targets the above mentioned missing elements in previous rehabilitation efforts. The present pilot study aims to assess the feasibility, acceptability, and preliminary efficacy of this program in childhood cancer survivors with cognitive impairment in preparation for a large-scale randomized controlled trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pediatric Cancer, Cognitive Dysfunction
Keywords
Pediatric Cancer, Cognitive Dysfunction, Neuropsychological Rehabilitation, Neurobehavioral Impairment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ImPACT program
Arm Type
Experimental
Arm Description
The ImPACT program consists of 8 weekly 1-hour sessions with homework between sessions.
Intervention Type
Behavioral
Intervention Name(s)
ImPACT
Intervention Description
During the ImPACT program, the childhood cancer survivor and at least one parent collaborates on: Becoming aware of the child's core strengths and difficulties Helping the child to be optimally responsive to the guidance of the parent(s), and Creating compensatory strategies to respond to real-world manifestations of the child's difficulties and helping the child implement these strategies at home.
Primary Outcome Measure Information:
Title
Parent-reported neurobehavioral functioning
Description
The parent-report screening version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 12 items: answer format range: 1-3; total score range: 12-36. Higher score indicates more impairment.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Parent-reported cognitive functioning
Description
The parent-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Secondary Outcome Measure Information:
Title
Parent-reported neurobehavioral functioning
Description
The parent-report version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 63 items: answer format range: 1-3; total score range: 63-189. Higher score indicates more impairment.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Parent-reported cognitive functioning
Description
The parent-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Child-reported neurobehavioral functioning
Description
The child-report version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 55 items: answer format range: 1-3; total score range: 55-165. Higher score indicates more impairment.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Child-reported neurobehavioral functioning
Description
The child-report version of the Behavior Rating Inventory of Executive Function 2nd Edition (BRIEF-2). 55 items: answer format range: 1-3; total score range: 55-165. Higher score indicates more impairment.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Child-reported cognitive functioning
Description
The child-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Child-reported cognitive functioning
Description
The child-report version of the Pediatric Perceived Cognitive Function (PedsPCF) Short Form. 7 items: answer format range 1-5; total score range: 7-35. Lower score indicates more impairment.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Parent-reported pediatric quality of life
Description
The parent-report version of the Pediatric Quality of Life (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate more impairment.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Parent-reported pediatric quality of life
Description
The parent-report version of the Pediatric Quality of Life Inventory (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate lower quality of life.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Child-reported pediatric quality of life
Description
The child-report version of the Pediatric Quality of Life (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate more impairment.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Child-reported pediatric quality of life
Description
The child-report version of the Pediatric Quality of Life (PedsQL) Core and Cancer scale. 23 items for the Core Scale, 25 items for the Cancer Scale: answer format range: 0-4; total score range: 0-100 (both scales). Lower scores indicate more impairment.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Parent-reported pediatric anxiety and depression
Description
The parent-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Parent-reported pediatric anxiety and depression
Description
The parent-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Child-reported pediatric anxiety and depression
Description
The child-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Child-reported pediatric anxiety and depression
Description
The child-report version of the Revised Children's Anxiety and Depression Scale (CADS) Short Form. 47 items: answer format range: 0-3; total score range: 0-27 (social phobia and panic disorder subscales), 0-30 (major depressive disorder subscale), 0-21 (social anxiety disorder subscale), 0-18 (generalized anxiety disorder and obsessive compulsive disorder subscales). Higher scores indicate more anxiety and depression.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Parent-reported pediatric fatigue
Description
The parent-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Parent-reported pediatric fatigue
Description
The parent-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Child-reported pediatric fatigue
Description
The child-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Child-reported pediatric fatigue
Description
The child-report version of the Pediatric Quality of Life - Multidimensional Fatigue Scale (PedsQL-MFS). 18 items: answer format range 0-4; total score range: 0-100. Lower score indicates more fatigue.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Parent sense of competence
Description
The Parenting Sense of Competence Scale (PSC scale).17 items: answer format range 1-6; total score range: 16-102. Higher score indicates more competence.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Parent sense of competence
Description
The Parenting Sense of Competence Scale (PSC scale). 17 items: answer format range 1-6; total score range: 16-102. Higher score indicates more competence.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Title
Parent-reported participant motivation
Description
The 7-item interest/enjoyment subscale of the Intrinsic Motivation Inventory (IMI). 7 items: answer format range 1-7; total score range: 1-7. Higher score indicates more motivation.
Time Frame
After last session (approximately 9 weeks after Baseline assessment (T1): Post-intervention, T3)
Title
Child-reported participant motivation
Description
The 7-item interest/enjoyment subscale of the Intrinsic Motivation Inventory (IMI). 7 items: answer format range 1-7; total score range: 1-7. Higher score indicates more motivation.
Time Frame
After last session (approximately 9 weeks after Baseline assessment (T1): Post-intervention, T3))
Title
Parent-reported participant satisfaction
Description
The Client Satisfaction Questionnaire (CSQ-8). 8 items: answer format range 1-4; total score range: 8-32. Higher score indicates better satisfaction.
Time Frame
After last session (approximately 9 weeks after Baseline assessment (T1): Post-intervention, T3)
Title
Child-reported participant satisfaction
Description
The Client Satisfaction Questionnaire (CSQ-8). 8 items: answer format range 1-4; total score range: 8-32. Higher score indicates better satisfaction.
Time Frame
After last session (approximately 9 weeks after Baseline assessment (T1): Post-intervention, T3)
Title
Objective cognitive functioning (Child only)
Description
Standard neuropsychological test battery. Different scoring formats.
Time Frame
Baseline (T1) to after last session (approximately 9 weeks later: Post-intervention, T3)
Title
Objective cognitive functioning (Child only)
Description
Standard neuropsychological test battery. Different scoring formats.
Time Frame
Baseline (T1) to 9 week after post-intervention (approximately 18 weeks later: Follow-up, T4)
Other Pre-specified Outcome Measures:
Title
Qualitative Interviews
Description
Following the T4 assessment, the child and parent(s) will be invited to participate in a 30-minutes semi-structured, audio recorded interview.
Time Frame
9 week after post-intervention (approximately 18 weeks after Baseline assessment (T1): Follow-up, T4)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cancer diagnosis of a leukemia, lymphoma, or central nervous system tumor Completed primary treatment at least 6 months ago Not terminally ill Attend school Living with one or more parents who speak Danish and are willing to co-participate Screened as having parent-reported cognitive and/or neurobehavioral impairment Exclusion Criteria: • Confounding diagnosed or suspected psychiatric or medical condition unrelated to the cancer or its treatment that might contribute to cognitive or neurobehavioral impairment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cecilie R Buskbjerg, PhD
Phone
+4529842526
Email
cdrc@psy.au.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Lisa M Wu, PhD
Phone
+4531221712
Email
lisa.wu@aias.au.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa M Wu, PhD
Organizational Affiliation
University of Aarhus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cecilie R Buskbjerg, Ph.D.
Phone
+45 29842526
Email
cdrc@psy.au.dk

12. IPD Sharing Statement

Plan to Share IPD
No

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Engaging Parents in Neuropsychological Rehabilitation for Childhood Cancer Survivors: The ImPACT Program - A Pilot Study

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