Cargando…

Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone

BACKGROUND: ADHD is prevalent in adults and frequently associated with impairment and distress. While medication is often the first line of treatment a high proportion of people with the condition are not fully treated by medication alone, cannot tolerate medication or do not wish to take it. Prelim...

Descripción completa

Detalles Bibliográficos
Autores principales: Dittner, Antonia J, Rimes, Katharine A, Russell, Ailsa J, Chalder, Trudie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158100/
https://www.ncbi.nlm.nih.gov/pubmed/25207986
http://dx.doi.org/10.1186/s12888-014-0248-1
_version_ 1782333984370327552
author Dittner, Antonia J
Rimes, Katharine A
Russell, Ailsa J
Chalder, Trudie
author_facet Dittner, Antonia J
Rimes, Katharine A
Russell, Ailsa J
Chalder, Trudie
author_sort Dittner, Antonia J
collection PubMed
description BACKGROUND: ADHD is prevalent in adults and frequently associated with impairment and distress. While medication is often the first line of treatment a high proportion of people with the condition are not fully treated by medication alone, cannot tolerate medication or do not wish to take it. Preliminary studies suggest that psychosocial approaches are a promising adjunctive or alternative treatment option. To date, individual cognitive-behaviour therapy (CBT) has been found to be efficacious in three randomized controlled trials (RCTs). There is a need for more RCTs to be carried out in order to replicate these results in different sites, to further investigate the acceptability and feasibility of CBT in this population and to further develop CBT approaches based on a psychological model. This randomized controlled trial investigates the efficacy of individual, formulation-based CBT when added to treatment-as-usual as compared with treatment as usual alone. METHODS/DESIGN: Sixty patients with a diagnosis of adult ADHD attending a specialist clinic are randomly allocated to 1 of 2 treatments, ‘Treatment as Usual’ (TAU) or TAU plus 16 sessions individual CBT (TAU + CBT). In the TAU + CBT, the first 15 sessions take place over 30 weeks with a 16th ‘follow-up’ session at 42 weeks. Outcomes are assessed at 30 weeks and 42 weeks following randomization. The two primary outcomes are self-rated ADHD symptoms and functioning (occupational and social). Secondary outcomes include distress, mood, ADHD-related cognitions, ADHD-related behaviours and informant-rated ADHD symptoms. The primary analysis will include all participants for whom data is available and will use longitudinal regression models to compare treatments. Secondary outcomes will be analysed similarly. DISCUSSION: The results of the study will provide information about a) whether CBT adds benefit over and above TAU for ADHD and, b) if CBT is found to be efficacious, potential mechanisms of change and predictors of efficacy. TRIAL REGISTRATION: Current Controlled Trials ISRCTN03732556, assigned 04/11/2010
format Online
Article
Text
id pubmed-4158100
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-41581002014-09-10 Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone Dittner, Antonia J Rimes, Katharine A Russell, Ailsa J Chalder, Trudie BMC Psychiatry Study Protocol BACKGROUND: ADHD is prevalent in adults and frequently associated with impairment and distress. While medication is often the first line of treatment a high proportion of people with the condition are not fully treated by medication alone, cannot tolerate medication or do not wish to take it. Preliminary studies suggest that psychosocial approaches are a promising adjunctive or alternative treatment option. To date, individual cognitive-behaviour therapy (CBT) has been found to be efficacious in three randomized controlled trials (RCTs). There is a need for more RCTs to be carried out in order to replicate these results in different sites, to further investigate the acceptability and feasibility of CBT in this population and to further develop CBT approaches based on a psychological model. This randomized controlled trial investigates the efficacy of individual, formulation-based CBT when added to treatment-as-usual as compared with treatment as usual alone. METHODS/DESIGN: Sixty patients with a diagnosis of adult ADHD attending a specialist clinic are randomly allocated to 1 of 2 treatments, ‘Treatment as Usual’ (TAU) or TAU plus 16 sessions individual CBT (TAU + CBT). In the TAU + CBT, the first 15 sessions take place over 30 weeks with a 16th ‘follow-up’ session at 42 weeks. Outcomes are assessed at 30 weeks and 42 weeks following randomization. The two primary outcomes are self-rated ADHD symptoms and functioning (occupational and social). Secondary outcomes include distress, mood, ADHD-related cognitions, ADHD-related behaviours and informant-rated ADHD symptoms. The primary analysis will include all participants for whom data is available and will use longitudinal regression models to compare treatments. Secondary outcomes will be analysed similarly. DISCUSSION: The results of the study will provide information about a) whether CBT adds benefit over and above TAU for ADHD and, b) if CBT is found to be efficacious, potential mechanisms of change and predictors of efficacy. TRIAL REGISTRATION: Current Controlled Trials ISRCTN03732556, assigned 04/11/2010 BioMed Central 2014-09-03 /pmc/articles/PMC4158100/ /pubmed/25207986 http://dx.doi.org/10.1186/s12888-014-0248-1 Text en © Dittner et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Dittner, Antonia J
Rimes, Katharine A
Russell, Ailsa J
Chalder, Trudie
Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone
title Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone
title_full Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone
title_fullStr Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone
title_full_unstemmed Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone
title_short Protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult ADHD as a supplement to treatment as usual, compared with treatment as usual alone
title_sort protocol for a proof of concept randomized controlled trial of cognitive-behavioural therapy for adult adhd as a supplement to treatment as usual, compared with treatment as usual alone
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158100/
https://www.ncbi.nlm.nih.gov/pubmed/25207986
http://dx.doi.org/10.1186/s12888-014-0248-1
work_keys_str_mv AT dittnerantoniaj protocolforaproofofconceptrandomizedcontrolledtrialofcognitivebehaviouraltherapyforadultadhdasasupplementtotreatmentasusualcomparedwithtreatmentasusualalone
AT rimeskatharinea protocolforaproofofconceptrandomizedcontrolledtrialofcognitivebehaviouraltherapyforadultadhdasasupplementtotreatmentasusualcomparedwithtreatmentasusualalone
AT russellailsaj protocolforaproofofconceptrandomizedcontrolledtrialofcognitivebehaviouraltherapyforadultadhdasasupplementtotreatmentasusualcomparedwithtreatmentasusualalone
AT chaldertrudie protocolforaproofofconceptrandomizedcontrolledtrialofcognitivebehaviouraltherapyforadultadhdasasupplementtotreatmentasusualcomparedwithtreatmentasusualalone