MedPath

Internet-administered, guided, psychological support (ENGAGE) for parents of children previously treated for cancer

Not Applicable
Completed
Conditions
Posttraumatic stress, depression, anxiety
Mental and Behavioural Disorders
Registration Number
ISRCTN57233429
Lead Sponsor
ppsala University
Brief Summary

2018 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/29903802 protocol 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34142662/ intervention development (added 21/06/2021) 2022 Other publications in https://pubmed.ncbi.nlm.nih.gov/35365530/ nested cross-sectional survey (added 04/04/2022) 2022 Results article in https://doi.org/10.1002/cam4.5377 (added 22/11/2022) 2024 Other publications in https://pubmed.ncbi.nlm.nih.gov/38846368/ E-therapists' views qualitative study (added 07/06/2024)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
72
Inclusion Criteria

Parents/caregivers (adults, both mothers and fathers) will be included according to:
1. Parent of a child diagnosed with cancer when 0-18 years who has completed cancer treatment 3 months to 5 years previously
2. Resides in Sweden
3. Able to read and understand text in Swedish
4. Has access to e-mail, the internet, and a mobile telephone and/or Bank ID
5. Self-reports a need for psychological support related to the child’s cancer disease and treatment

Exclusion Criteria

The following exclusion criteria will be used:
1. Self-reported or clinician-assessed (based on the M.I.N.I neuropsychiatric interview) symptoms of a severe and enduring mental health difficulty
2. Self-reported or clinician-assessed (based on the M.I.N.I neuropsychiatric interview) misuse of alcohol, street drugs, and/or prescription medication
3. Acutely suicidal
4. Currently attending psychological treatment. Those excluded due to a severe and enduring mental health difficulty, substance misuse, and/or acute suicidality will be guided to appropriate healthcare services

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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