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Life Beyond Trauma: 1-on-1 e-Health Program for Parents of Neurodiverse Children

Primary Purpose

Post Traumatic Stress Injury, Post Traumatic Stress Disorder

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
e-Net for Parents of Neurodiverse Children
Sponsored by
IWK Health Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post Traumatic Stress Injury

Eligibility Criteria

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

Inclusion Criteria: Parent/Caregivers must meet the following criteria to be eligible to move on to Consent

  1. Be a parent/caregiver of a neurodiverse child
  2. Be at least 18 years of age
  3. Be able to understand spoken and written English at a Grade 8 level
  4. Fulfill the criteria of full or subclinical PTSI according to DSM-5, measured with the Life Events Checklist for DSM-5, the Parent Trauma Checklist and the PTSD Checklist for DSM-5. For this they have to report at least one traumatic event in the LEC-5 or the Stressful Life Experiences of Parents Checklist. To fulfill all PTSI criteria, the participant additionally needs to respond with "moderately" or higher in at least one item for the criteria B and C and two items for criteria D and E. Subclinical PTSI is fulfilled if the participant meets all but one criterion of B, C, D, or E is not met.
  5. Have access to a computer with high speed Internet
  6. Live in Canada
  7. Commit to the requirements of taking part in the study (12 weekly coaching calls)

Exclusion Criteria:

  1. Acute suicidal behavior or other extreme forms of self-destructive behavior
  2. Moderate to severe symptoms of dissociation
  3. Acute psychotic symptoms
  4. Previously participated in exposure intervention for PTSI/PTSD

Sites / Locations

  • IWK Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Immediate e-NET Group

Wait List Control Group

Arm Description

Parents of neurodiverse children with PTSI will receive e-NET immediately after the baseline survey

Parents of neurodiverse children with PTSI will receive e-NET 3 months after the baseline survey

Outcomes

Primary Outcome Measures

Change in PTSI symptoms
PTSD symptoms are measured with the PTSD Checklist - 5 (PCL-5). Respondents are asked to rate how bothered they have been by each of 20 items in the past month on a 5- point Likert scale ranging from 0-4. Items are summed to provide a total severity score. Higher scores indicate a worse outcome

Secondary Outcome Measures

Change in Overall Health
General health will be measured with the questionnaire PROMIS Global Health Caregiver's general health
Change in Depression Symptoms
Depression symptoms will be measured with the Patient Health Questionnaire (PHQ-9)
Change in overall functionality
Functionality will be measured with the Sheehan Disability Scale (SDS). SDS is measured on a 10-point scale (0-9). Higher score indicates a worse outcome.
Posttraumatic Growth
Posttraumatic growth will be measures using the Posttraumatic Growth Inventory - Short Form (PTGI ). The PTGI is measured on a 6-point Likert scale (score 0-5). Higher score indicates a better outcome.
Parent-child Relationship
The parent-child relationship will be measured with the Parent and Family Adjustment Scales (PAFAS). Items are rated from 0 to 3. Note that shaded items in the scoring key below must be reverse scored (i.e. 0=3, 1=2, 2=1, 3=0) before summing the Total Score. High scores indicate worse outcome.
Satisfaction with Lifeline Tool
The satisfaction with Lifeline Tool (self-constructed) will be measured with a self-constructed 3-item usability questionnaire. It is scored on a five point scale. Items are rated from 0-4. Higher score indicates better outcome.
Change in Anxiety Symptoms
Anxiety Symptoms are measured with the Generalized Anxiety Disorder (GAD-7). Items are scored on a four point scale, items are rated from 0-3. Higher score indicates better outcome.
Change in Physical Health Symptoms
Physical Health symptoms will be assessed with the Patient Health Questionnaire Physical Symptoms (PHQ-15). Items are scored on a three point scale, items are rated from 0-2. Higher score indicates worse outcome.
Adverse Events
Adverse events will be assessed with a self-constructed questionnaire for adverse events, the course of symptoms during intervention and general distress.
Therapeutic Alliance
The interaction between coach and client will be assessed through the Therapeutic Alliance- Working Alliance Inventory - Short Form Revised (WAI-SR)
Participant Satisfaction
Client satisfaction will be assessed with the Client Satisfaction Questionnaire (CSQ-8) and some additional (self-constructed) qualitative questions. CAQ-8 Items are scored on a four point scale, items are rated from 0-3. Higher score indicates worse outcome.

Full Information

First Posted
March 23, 2020
Last Updated
March 29, 2022
Sponsor
IWK Health Centre
Collaborators
Canadian Institutes of Health Research (CIHR), Child-Bright Network
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1. Study Identification

Unique Protocol Identification Number
NCT04385927
Brief Title
Life Beyond Trauma: 1-on-1 e-Health Program for Parents of Neurodiverse Children
Official Title
Life Beyond Trauma: 1-on-1 e-Health Program for Parents of Neurodiverse Children
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
June 29, 2020 (Actual)
Primary Completion Date
August 31, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IWK Health Centre
Collaborators
Canadian Institutes of Health Research (CIHR), Child-Bright Network

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
Parents of neurodiverse children are more likely to experience traumatic events related to the care of their child/children. This increases the probability to experience Posttraumatic Stress Injury (PTSI). However, interventions addressing PTSI symptoms in parents are rare. In this research project the study investigators will test the feasibility and efficacy of e-NET, a distance-delivered, exposure-based intervention for PTSI adapted to the needs of parents of neurodiverse children. E-NET is an adapted version of the Narrative Exposure Therapy (NET), an evidence-based intervention approach for individuals with PTSI who have experienced repeated or continuous trauma. The intervention will be conducted via videoconferencing with trained paraprofessionals. During the intervention a narrative of both positive and negative (traumatic) experiences in the parents' life will be created. The intervention contains approx. 12 one-on-one sessions with a trained paraprofessional via videoconferencing. The study design is a waitlist control group design. Approx. 20 participants will receive e-NET directly after the baseline survey and 20 participants will receive e-NET approx. 3 months after the baseline survey. To test the efficacy of the intervention, participants will fill out surveys about PTSI and other mental health symptoms before, directly after, and 2 and 6 months after the intervention. Adverse events and distress will be assessed in every session. As part of the baseline, participants will complete the survey "Surviving and Thriving in Parenting Neurodiverse Children" to determine their eligibility for the intervention. Main eligibility criterion is the presence of PTSI symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Traumatic Stress Injury, Post Traumatic Stress Disorder

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Immediate e-NET Group
Arm Type
Experimental
Arm Description
Parents of neurodiverse children with PTSI will receive e-NET immediately after the baseline survey
Arm Title
Wait List Control Group
Arm Type
Experimental
Arm Description
Parents of neurodiverse children with PTSI will receive e-NET 3 months after the baseline survey
Intervention Type
Behavioral
Intervention Name(s)
e-Net for Parents of Neurodiverse Children
Intervention Description
One-on-one distance coached intervention; approx. 12 sessions at 60-90 minutes.
Primary Outcome Measure Information:
Title
Change in PTSI symptoms
Description
PTSD symptoms are measured with the PTSD Checklist - 5 (PCL-5). Respondents are asked to rate how bothered they have been by each of 20 items in the past month on a 5- point Likert scale ranging from 0-4. Items are summed to provide a total severity score. Higher scores indicate a worse outcome
Time Frame
Baseline, Immediately Post- intervention, 2 months post-intervention, 6 months post-intervention
Secondary Outcome Measure Information:
Title
Change in Overall Health
Description
General health will be measured with the questionnaire PROMIS Global Health Caregiver's general health
Time Frame
Baseline, Wait-list Baseline; through study completion, an average of 12 weeks; Immediately Post-assessment; 2 month follow up; 6 month follow up
Title
Change in Depression Symptoms
Description
Depression symptoms will be measured with the Patient Health Questionnaire (PHQ-9)
Time Frame
Baseline, Immediately Post-assessment, 2 month follow up, 6 month follow up
Title
Change in overall functionality
Description
Functionality will be measured with the Sheehan Disability Scale (SDS). SDS is measured on a 10-point scale (0-9). Higher score indicates a worse outcome.
Time Frame
Baseline; Wait list Baseline, Immediately Post intervention; 2 month follow up; 6 month follow up
Title
Posttraumatic Growth
Description
Posttraumatic growth will be measures using the Posttraumatic Growth Inventory - Short Form (PTGI ). The PTGI is measured on a 6-point Likert scale (score 0-5). Higher score indicates a better outcome.
Time Frame
Baeline; Wait list Baseline; Immediately Post intervention; 2 month follow up; 6 month follow up
Title
Parent-child Relationship
Description
The parent-child relationship will be measured with the Parent and Family Adjustment Scales (PAFAS). Items are rated from 0 to 3. Note that shaded items in the scoring key below must be reverse scored (i.e. 0=3, 1=2, 2=1, 3=0) before summing the Total Score. High scores indicate worse outcome.
Time Frame
Baseline; Wait list Baseline; Immediately Post intervention; 2 month follow up; 6 month follow up
Title
Satisfaction with Lifeline Tool
Description
The satisfaction with Lifeline Tool (self-constructed) will be measured with a self-constructed 3-item usability questionnaire. It is scored on a five point scale. Items are rated from 0-4. Higher score indicates better outcome.
Time Frame
During week 1 of intervention
Title
Change in Anxiety Symptoms
Description
Anxiety Symptoms are measured with the Generalized Anxiety Disorder (GAD-7). Items are scored on a four point scale, items are rated from 0-3. Higher score indicates better outcome.
Time Frame
Baseline, Immediately Post-assessment, 2 month follow up, 6 month follow up
Title
Change in Physical Health Symptoms
Description
Physical Health symptoms will be assessed with the Patient Health Questionnaire Physical Symptoms (PHQ-15). Items are scored on a three point scale, items are rated from 0-2. Higher score indicates worse outcome.
Time Frame
Baseline; throughout study completion, approximately 12 week; Immediately Post-assessment; 2 month follow up; 6 month follow up
Title
Adverse Events
Description
Adverse events will be assessed with a self-constructed questionnaire for adverse events, the course of symptoms during intervention and general distress.
Time Frame
throughout study completion, approximately 12 weeks; immediately post intervention
Title
Therapeutic Alliance
Description
The interaction between coach and client will be assessed through the Therapeutic Alliance- Working Alliance Inventory - Short Form Revised (WAI-SR)
Time Frame
Immediately post intervention
Title
Participant Satisfaction
Description
Client satisfaction will be assessed with the Client Satisfaction Questionnaire (CSQ-8) and some additional (self-constructed) qualitative questions. CAQ-8 Items are scored on a four point scale, items are rated from 0-3. Higher score indicates worse outcome.
Time Frame
Immediately Post intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Parent/Caregivers must meet the following criteria to be eligible to move on to Consent Be a parent/caregiver of a neurodiverse child Be at least 18 years of age Be able to understand spoken and written English at a Grade 8 level Fulfill the criteria of full or subclinical PTSI according to DSM-5, measured with the Life Events Checklist for DSM-5, the Parent Trauma Checklist and the PTSD Checklist for DSM-5. For this they have to report at least one traumatic event in the LEC-5 or the Stressful Life Experiences of Parents Checklist. To fulfill all PTSI criteria, the participant additionally needs to respond with "moderately" or higher in at least one item for the criteria B and C and two items for criteria D and E. Subclinical PTSI is fulfilled if the participant meets all but one criterion of B, C, D, or E is not met. Have access to a computer with high speed Internet Live in Canada Commit to the requirements of taking part in the study (12 weekly coaching calls) Exclusion Criteria: Acute suicidal behavior or other extreme forms of self-destructive behavior Moderate to severe symptoms of dissociation Acute psychotic symptoms Previously participated in exposure intervention for PTSI/PTSD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick McGrath, PhD
Organizational Affiliation
IWK Health Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Elisa Kaltenbach, PhD
Organizational Affiliation
IWK Health Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
IWK Health Centre
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3K6R8
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34868484
Citation
Kaltenbach E, Chisholm M, Xiong T, Thomson D, Crombach A, McGrath PJ. Online narrative exposure therapy for parents of children with neurodevelopmental disabilities suffering from posttraumatic stress symptoms - study protocol of a randomized controlled trial. Eur J Psychotraumatol. 2021 Nov 21;12(1):1991650. doi: 10.1080/20008198.2021.1991650. eCollection 2021.
Results Reference
derived

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Life Beyond Trauma: 1-on-1 e-Health Program for Parents of Neurodiverse Children

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