Depression Clinical Trial
Official title:
Efficacy of Narrative Reformulation During Cognitive Analytic Therapy: A Randomized Dismantling Trial
| Verified date | November 2016 |
| Source | University of Sheffield |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United Kingdom: National Health Service |
| Study type | Interventional |
Narrative reformulation (NR) is an active ingredient of cognitive analytic therapy (CAT) which is assumed to increase engagement and improve outcomes. This trial sought to test these claims. A randomized and controlled dismantling trial method has been designed to investigate treatments outcomes for depressed patients receiving CAT in an Improving Access to Psychological Therapies service. Participants will be randomized to either treatment as usual (full-CAT) or CAT minus narrative reformulation (CAT-NR). The primary outcome measure is the Patient Health Questionnaire (PHQ-9), with secondary outcome measures of anxiety, functioning, helpfulness and the alliance. Outcomes will be assessed at screening, every treatment session and at 8-weeks follow-up. The trial will enable as assessment of the utility of NR during CAT. and whether CAT appears suitable for treating depression in Primary Care.
| Status | Completed |
| Enrollment | 95 |
| Est. completion date | January 2015 |
| Est. primary completion date | January 2014 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion criteria were: 1. clinical diagnosis of depression (conducted using DSM-IV criteria) 2. participants needed to reach caseness (i.e. score 10-21) on the PHQ-9 Exclusion criteria were: 1. a PHQ-9 score <10 2. not meeting DSM criteria for depression 3. significant risk issues 4. co-morbid anxiety disorder 5. previous in-patient admission 6. significant amount of previous contact with mental health services 7. visual impairment 8. non-English speaking 9. history of overdoses/self-injury 10. currently abusing substances |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Clinical Psychology Unit, Department of Psychology, Uni of Sheffield | Sheffield |
| Lead Sponsor | Collaborator |
|---|---|
| University of Sheffield |
United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in depression at end of treatment via the Patient Health Questionnaire-9 (PHQ-9) | This measure screens patients in Primary Care for depression. Scores on the PHQ-9 range from 0-27, a score of >10 on the PHQ9 used as a cut-off point for identifying clinical caseness. The PHQ-9 is widely recognised as a valid and reliable measure of depressive symptoms items mirror DSM criteria for symptoms of depression. | At 16 weeks. | No |
| Secondary | Change in anxiety at end of treatment via the Generalized Anxiety Disorder-7 (GAD-7) | This measure screens patients in Primary Care for the presence of generalized anxiety, with the recommended cut-off point for caseness being >10. The GAD-7 is recommended as a useful tool for assessing initial anxious symptom severity and also monitoring outcomes in Primary Care. | At 16 weeks | No |
| Secondary | Change in functioning at the end of treatment on the Work and Social Adjustment Scale (WSAS) | The WSAS measures the impact of mental health difficulties on aspects of daily functioning. Scores on the WSAS range from 0-40, a higher score on the scale indicates a higher level of disability on daily functioning. The WSAS is used as a measure of functional impairment in Primary Care. | At 16 weeks | No |
| Secondary | Change in the therapeutic alliance at the end of treatment on the Working Alliance Inventory-Short (WAI-S) | This measure assesses the strength of the therapeutic alliance across three subscales -tasks, goal agreement and quality of therapeutic bond. The WAI-S has been found to have a good internal reliability and predictive validity. | At 16 weeks | No |
| Secondary | Change in the helpfulness of the therapy via the the Helpful Aspects of Therapy (HAT) | This is measure gains quantitative and qualitative information on the patient's perceptions of the helpfulness of individual sessions and asks ratings of helpful and/or impeding events. | At 16 weeks | No |
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