Last reviewed · How we verify
NCT02307097: RCT of CBB/CBT
RCT of Bibliotherapy for Social Anxiety Disorder as a Prelude to CBT in IAPT
NA trial testing Cognitive-Behavioural Bibliotherapy in Bibliotherapy in 114 participants. Completed in 1 October 2017.
1 October 2017
Quick facts
| Lead sponsor | Solent NHS Trust |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 114 |
| Start date | 1 January 2016 |
| Primary completion | 1 October 2017 |
| Estimated completion | 1 October 2017 |
| Sites | 1 location across United Kingdom |
Drugs / interventions tested
- Cognitive-Behavioural Bibliotherapy
- Cognitive-Behavioural Therapy
- WAIT
Conditions studied
- Bibliotherapy — all drugs for Bibliotherapy →
- Social Anxiety Disorder — all drugs for Social Anxiety Disorder →
- Cognitive Behavioral Therapy — all drugs for Cognitive Behavioral Therapy →
Sponsor
Solent NHS Trust
Who can join
Adults 18 to 80, any sex, with Bibliotherapy or Social Anxiety Disorder. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The efficacy of high-intensity Cognitive-Behavioural Therapy (CBT) for social anxiety disorder is well established (Mayo-Wilson et al., 2014) and it is recommended by the National Institute of Health and Clinical Excellence (NICE) as the first-line psychological intervention for social anxiety disorder. The treatment aims to modify several maintenance factors (e.g., self-focused attention) that are specified in cognitive models of social anxiety disorder (e.g., Clark \& Wells, 1995). Cognitive-behavioural self-help treatments for social anxiety disorder have been developed to overcome various accessibility issues (e.g., long wait-lists, and the patient's need to avoid social situations, etc) associated with high-intensity CBT (Abramowitz et al., 2009; Carlbring et al., 2007) but a recent network meta-analysis (Mayo-Wilson et al., 2014) identified the former as less cost-effective than the later and thus, they are not recommended as standalone treatments. However, the potential benefit of cognitive-behavioural self-help treatments for social anxiety disorder within a stepped-care recovery model as a prelude to high-intensity CBT has not been formally evaluated. The aim of this study is to evaluate a seminal Cognitive-Behavioural Bibliotherapy\* (CBB; "pure self-help" book) - 'Overcoming Social Anxiety \& Shyness' (Butler, 2009) - for patients with social anxiety disorder while on the wait-list for high-intensity CBT within an Improving Access to Psychological Therapies (IAPT) service, and to determine if some patients recover from CBB alone or whether there may be a reduction in the average number of high-intensity CBT sessions for those patients who subsequently require further treatment. The study is funded by Constable \& Robinson, Kellogg College (University of Oxford) and Talking Change (Solent NHS Trust). \* The Reading Well Books on Prescription scheme with funding from the Arts Council England enables general practitioners (GPs) and mental health professionals to prescribe seminal CBBs for patients with mood and anxiety disorders. The books are accessed free of charge via local libraries. The scheme works within NICE guidelines and it is support by the Royal Colleges of GPs, Nursing and Psychiatrists, the British Association for Behavioural and Cognitive Psychotherapies and the Department of Health through its IAPT programme.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT02307097
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Bibliotherapy
Currently open trials in the same condition.
- NCT06652880 — Digital Support Intervention for Pregnant People with Opioid Use Disorders · EARLY_PHASE1 · active not recruiting
Other Solent NHS Trust trials
Trials by the same sponsor.
- NCT03151941 — Respiratory Monitoring of Intrathecal Baclofen- a Feasibility Study · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02307097 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Solent NHS Trust
- Last refreshed: 10 October 2017
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02307097.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing