Pilot evaluation of integrated CBT for depressio
- Conditions
- Specialty: Primary care, Primary sub-specialty: Mental HealthUKCRC code/ Disease: Mental Health/ Mood [affective] disordersMental and Behavioural DisordersMental Health/ Mood [affective] disorders
- Registration Number
- ISRCTN14850613
- Lead Sponsor
- niversity of Bristol
- Brief Summary
2020 pragmatic study results in http://dx.doi.org/10.1145/3313831.3376510 (added 18/06/2020)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 30
Longitudinal study:
1. Aged 18 years or older
2. Score =14 on Beck Depression Inventory (BDI-II; Beck et al., 1996)
3. Meet ICD-10 criteria for depression (CIS-R; Lewis et al., 1992; Lewis, 1994)
Therapists and Clinical Supervisors
Working as therapists and clinical supervisors to deliver or supervise the INTERACT integrated therapy for this (Phase 2) study.
Usability testing sessions
1. Aged 18 years or older
2. Have a history of depression
3. Have previously received high-intensity CBT for depression (online and/or face-to-face)
Longitudinal study with primary care patients:
1. Major alcohol or substance use problems (in the past year)
2. Have bipolar disorder, psychosis or dementia
3. Cannot complete questionnaires unaided
4. Are currently receiving CBT or other psychotherapy or secondary care for depression
5. Have received individual, high-intensity CBT in past 4 years
6. Taking part in another research study
7. Need an interpreter
Usability testing sessions with service-users:
1. Unable to complete questionnaires
2. Have not received CBT for depression
3. Are currently receiving treatment from a psychiatrist for depression
4. Have a history of bipolar disorder, schizophrenia or personality disorder
5. Have a history of substance misuse/alcohol addiction (in the past year)
6. Are currently not well enough to attend a session
7. Have taken part in Phase 1 of the INTERACT study
Therapists and clinical supervisors
No exclusion criteria
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method