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Clinical Trials/ISRCTN15124804
ISRCTN15124804
Active, not recruiting
未知

Developing precision computerised cognitive behavioural therapy for adolescent depression: a pilot and feasibility randomised controlled trial (SPARX-UK)

niversity of Nottingham0 sites120 target enrollmentJanuary 16, 2023

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Nottingham
Enrollment
120
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

2024 Protocol article in https://pubmed.ncbi.nlm.nih.gov/38532490/ (added 27/03/2024)

Registry
who.int
Start Date
January 16, 2023
End Date
March 30, 2025
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Nottingham

Eligibility Criteria

Inclusion Criteria

  • 1\. Adolescents aged 11 to 19 years on the date of consent referred to CAMHS or MHST
  • 2\. Presented at CAMHS/MHST for treatment with symptoms indicative of mild to moderate depressive disorder as confirmed by the PHQ\-A
  • 3\. Able to provide written consent or, if under age 16, written parental consent and written/verbal child assent
  • 4\. Has access to a computer with internet access or smartphone or device to use SPARX and must be able to install and log in
  • 5\. Parent and adolescent able to read and write in English

Exclusion Criteria

  • 1\. Depression assessed as being too severe to make SPARX an appropriate intervention as confirmed by the PHQ\-A
  • 2\. High risk of current self\-harm or suicide as confirmed by a clinician
  • 3\. Intellectual disability or physical limitations precluding the use of SPARX
  • 4\. Had (in the past three months) or currently having treatment with CBT/interpersonal therapy
  • 5\. Has another major mental health disorder (e.g., psychosis, eating disorder) where the primary focus was not depression as confirmed by a clinician or DAWBA
  • 6\. Safeguarding concerns that are currently not being managed (i.e., the young person is the subject of a safeguarding investigation) as confirmed by a clinician

Outcomes

Primary Outcomes

Not specified

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