MedPath

A trial of ‘cognitive remediation therapy’ to improve thinking skills and everyday functioning for people with bipolar disorder

Not Applicable
Conditions
Bipolar disorder
Mental and Behavioural Disorders
Registration Number
ISRCTN10362331
Lead Sponsor
King's College London
Brief Summary

2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37968619/ (added 16/11/2023)

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
250
Inclusion Criteria

1. Have a confirmed diagnosis of bipolar disorder type I or II.
2. Be aged between 18 and 65 years.
3. Be euthymic (not in a mood episode) for at least 1 month.
4. Be able to use a computerised device (e.g., computer / smartphone).

Exclusion Criteria

Current participant exclusion criteria as of 04/05/2022:
1. Substance use diagnosis (abuse or dependence).
2. Risk of suicide.
3. Impairing neurological disorder or MCI.
4. Previous cognitive remediation therapy.
5. Unable to communicate fluently in English.
6. Intellectual disability.
7. Currently undergoing psychological therapy or planning imminent treatment change.
8. Non-provision of UK healthcare professional contact.
9. Unable to travel to one of the research sites on a regular basis over 25 weeks.
10. Unable to provide informed consent to participate.

Previous participant exclusion criteria:
1. Substance use diagnosis (abuse or dependence).
2. Risk of suicide.
3. Impairing neurological disorder or MCI.
4. Previous cognitive remediation therapy.
5. Unable to communicate fluently in English.
6. Intellectual disability.
7. Currently undergoing psychological therapy or planning imminent treatment change.
8. Non-provision of UK healthcare professional contact.
9. Unable to provide informed consent to participate.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Everyday functioning, assessed using the Functioning Assessment Short Test. This is measured at baseline, 13 and 25 weeks with the primary outcome timepoint as 25 weeks.
Secondary Outcome Measures
NameTimeMethod
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