Trial of Sertraline Versus Cognitive Behaviour Therapy for Generalised Anxiety (ToSCA)

RCT of Sertraline Versus Cognitive Behavioural Therapy for Anxiety Symptoms in People With Generalised Anxiety Disorder Who Have Failed to Respond to Low Intensity Psychological Interventions as Defined by the NICE GAD Guidelines

Generalised Anxiety Disorder (GAD) is common, causes unpleasant symptoms and impairs people's functioning. It is often chronic and may be accompanied by depression and other anxiety disorders. It is not currently clear whether medication or psychological therapy provides better long term outcomes for those not responding to simpler low intensity treatments so we propose to compare the clinical effectiveness of a pharmacological treatment (the drug Sertraline) with a Cognitive Behavioural Therapy (CBT) intervention.

Our hypothesis is that in people with GAD who have not responded to low intensity psychological interventions, CBT will lead to a greater improvement in their GAD symptoms as measured using the GAD-7 scale at 12 month follow-up than Sertraline.

Study Overview

• Status: Terminated
• Conditions: Generalised Anxiety Disorder
• Intervention / Treatment: Drug: Sertraline; Behavioral: Cognitive Behavioural Therapy

Detailed Description

The investigators propose to undertake a randomised controlled trial (RCT) to compare the clinical effectiveness in terms of symptoms and function of a pharmacological treatment (the SSRI Sertraline) prescribed at therapeutic doses, with a manualised psychological intervention (Cognitive Behavioural Therapy, CBT) delivered by trained psychological therapists to patients with persistent generalised anxiety disorder (GAD) which has not improved with low intensity psychological interventions as defined by NICE (the National Institute for Clinical Effectiveness).

The investigators will recruit people via the Increasing Access to Psychological Therapies (IAPT) service from up to 15 sites in England. People still scoring highly on an anxiety measure (GAD-7) despite having received a low intensity psychological intervention will be given a brief flyer about the trial. Names of those interested in taking part who have given written consent to having their details released will be passed to the research team and the IAPT staff will also let the research team know the name of the participant's general practice, with their permission.

The research team will then contact potential participants offering them an appointment for an interview/assessment to discuss the study, sending them a patient information sheet to reach them at least 48 hours beforehand. The study information will explain that the medication being evaluated, Sertraline, although not currently licensed for GAD was recommended by NICE on the basis of its effectiveness in clinical trials and that the study team will be available to clarify any issues arising from this.

At the baseline assessment patients will be asked to give informed consent by a member of the research team and both medical suitability (as confirmed by fax/secure email from the GP) and the meeting of other inclusion/exclusion criteria will be checked. Upon confirmation of eligibility, baseline assessments will be carried out by a member of the research team and consenting patients randomised to receive either the medication or CBT. The Chief Investigator or other medically qualified persons within the research team will review all eligibility information and confirm that the patient is eligible.

Eligible participants will be randomised via an independent web-based computerised system to one of two interventions. The research team will provide the relevant contact details/instructions to patients in order to initiate treatment. The trial interventions consist of: (a) The medication sertraline prescribed by their GP according to a trial protocol matching current clinical recommendations and within a dosage between 25 and 150mg daily. We will ask GPs to review patients regularly (at least 6 times in 12 months) and patients to take the medication for a year unless they have significant adverse effects. Side-effects will be regularly monitored. (b) The other intervention is CBT delivered by high intensity therapists from local IAPT services. They will provide 14 to 16 sessions of a manualised treatment developed for use in GAD and will be trained in its delivery. The primary outcome will be the GAD-7 score measured at 12 months. Participants will also be asked to complete this outcome measure by postal questionnaire at 3, 6 and 9 months, as well as a range of secondary outcomes.

• Study Type: Interventional
• Enrollment (Actual): 5
• Phase: Phase 4

Contacts and Locations

Study Locations

• United Kingdom
  • London, United Kingdom, WC1X 2DN
    • Camden & Islington (with Kingston)

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Aged 18 or above
• Positive score of 10+ on GAD-7
• Primary diagnosis of GAD as diagnosed on MINI
• Failure to respond to NICE defined low intensity psychological interventions

Exclusion Criteria:

• Inability to complete questionnaires due to insufficient English or cognitive impairment;
• Current major depression
• Other comorbid anxiety disorder(s) of more severity or distress to the participant than their GAD;
• Significant dependence on alcohol or illicit drugs;
• Comorbid psychotic disorder, bipolar disorder;
• Treatment with antidepressants in past 8 weeks or any high intensity psychological therapy within past 6 months;
• Currently on contraindicated medication: monoamine oxidase Inhibitors within the past 14 days or pimozide;
• Patients with poorly controlled epilepsy;
• Known allergies to the Investigational Medicinal Product (IMP) or excipients;
• Concurrent enrolment in another Investigational Medicinal Product trial;
• Severe hepatic impairment;
• Women who are currently pregnant or planning pregnancy or lactating
• Patient on anti-coagulants
• History of bleeding disorders

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
ACTIVE_COMPARATOR: Sertraline; The pharmacological arm of the trial is the Selective Serotonin Reuptake Inhibitor (SSRI) Sertraline, prescribed at a daily dose of between 25 and 150mg by the patient's general practitioner (GP). If the medication is well tolerated and associated with reported clinical improvement we are asking the patients in this arm to continue taking it for 12 months.	Drug: Sertraline; Sertraline will be prescribed by the patients' GP, starting at 25mg daily for 1-2 weeks and increasing to 50mg daily if tolerated. The GP should review the patient within the first 2 weeks, checking for acceptability, concordance and any side-effects, with further reviews at 6 and 12 weeks. We expect the usual treatment dose to be 50 to 100mg daily, although some may require 150mg. We will suggest that the GPs use their usual procedures to review the patient's progress, asking about and noting functional change as well as clinical improvement. Minimal improvement after 12 weeks at a maximal tolerated dose should prompt consideration of change of treatment. If there has been an adequate therapeutic benefit there should be further review at 26 and 52 weeks.; Other Names: SSRI
ACTIVE_COMPARATOR: Cognitive Behavioural Therapy (CBT); The psychological therapy arm of the trial is Cognitive Behavioural Therapy (CBT) delivered by high intensity psychological therapists from local IAPT services. They will provide 14 to 16 sessions of a manualised treatment developed specifically for use in GAD and will be trained in its delivery.	Behavioral: Cognitive Behavioural Therapy; CBT will consist of 14 (+ / - 2) weekly 50-minute sessions and will cover 6 treatment modules: psychoeducation and worry awareness training; re-evaluation of the usefulness of worry; uncertainty recognition and behavioural exposure; problem-solving training; written exposure; and relapse prevention. Sessions will be digitally recorded and a random 10% assessed for quality (fidelity to the manual and therapist competence) by an independent external assessor according to pre-specified criteria. Patient consent for this will be obtained as part of obtaining informed consent.; Other Names: CBT

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
GAD-7	A 7 item self-complete questionnaire with very good sensitivity (89%) and specificity (82%) for Generalised Anxiety Disorder (GAD).	GAD-7 score at 12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
GAD-7	A 7 item self-complete questionnaire with very good sensitivity (89%) and specificity (82%) for Generalised Anxiety Disorder (GAD).	GAD-7 score at 3 months
GAD-7	A 7 item self-complete questionnaire with very good sensitivity (89%) and specificity (82%) for Generalised Anxiety Disorder (GAD).	GAD-7 score at 6 months
GAD-7	A 7 item self-complete questionnaire with very good sensitivity (89%) and specificity (82%) for Generalised Anxiety Disorder (GAD).	GAD-7 score at 9 months
HAM-A	This is a 14 item observer rated anxiety scale which has been widely used, particularly in pharmacological studies widely used, particularly in pharmacological studies	HAM-A score at 12 months
Patient Health Questionnaire (PHQ-9)	This is a 9 item self-rate scale widely used to monitor the severity of depression.	PHQ-9 score at 3 months
Patient Health Questionnaire (PHQ-9)	This is a 9 item self-rate scale widely used to monitor the severity of depression.	PHQ-9 score at 6 months
Patient Health Questionnaire (PHQ-9)	This is a 9 item self-rate scale widely used to monitor the severity of depression.	PHQ-9 score at 9 months
Patient Health Questionnaire (PHQ-9)	This is a 9 item self-rate scale widely used to monitor the severity of depression.	PHQ-9 score at 12 months
Work and Social Activity Scale (WASAS)	This is a 5 item self-complete questionnaire which we will use to assess participants' difficulties with physical and social functioning	WASAS score at 12 months
Euroquol-5 item-3 level (EQ-5D-3L)	5 item, 3 level, self-completed measure of preference based generic health related quality of life. Utility scores calculated at each time point	Utility score at 3 months
Euroquol-5 item-3 level (EQ-5D-3L)	5 item, 3 level, self-completed measure of preference based generic health related quality of life. Utility scores calculated at each time point scores for Quality Adjusted Life Years	Utility score at 6 months
Euroquol-5 item-3 level (EQ-5D-3L)	5 item, 3 level, self-completed measure of preference based generic health related quality of life. Utility scores calculated at each time point scores for Quality Adjusted Life Years	Utility score at 9 months
Euroquol-5 item-3 level (EQ-5D-3L)	5 item, 3 level, self-completed measure of preference based generic health related quality of life. Utility scores calculated at each time point scores for Quality Adjusted Life Years	Utility score at 12 months
Employment and Social Care Questionnaire (ESC)	Relevant data on services used and productivity losses will be collected using this modified version of the Client Service Receipt Inventory	ESC score at 6 months
Employment and Social Care Questionnaire (ESC)	Relevant data on services used and productivity losses will be collected using this modified version of the Client Service Receipt Inventory	ESC score at 12 months
(CSQ) Client Satisfaction Questionnaire	We are going to use the Client Satisfaction Questionnaire, a brief 8-item self-complete questionnaire as our treatment acceptability measure.	CSQ score at 3 months
(CSQ) Client Satisfaction Questionnaire	We are going to use the Client Satisfaction Questionnaire, a brief 8-item self-complete questionnaire as our treatment acceptability measure.	CSQ score at 12 months
Patient preference rating scale	We are using a simple 4 item Likert scale used by our team in other studies	Patient preference rating scale score at 12 months

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Health service outcome - General practitioner (GP) contacts	We will collect relevant health service use data from both intervention arms at 12 months for the previous 12 months. This will include the number of GP contacts.	GP contacts at 12 months
Health service outcome - Practice nurse contacts	We will collect relevant health service use data from both intervention arms at 12 months for the previous 12 months. This will include the number of practice nurse contacts.	Practice nurse contacts at 12 months
Health service outcome - referrals to secondary care medical services	We will collect relevant health service use data from both intervention arms at 12 months for the previous 12 months. This will include the number of referrals to secondary care medical services	Referrals to secondary care medical services at 12 months
Health service outcome - referrals to psychological therapy services	We will collect relevant health service use data from both intervention arms at 12 months for the previous 12 months. This will include referrals to psychological therapy services.	Referrals to psychological therapy services at 12 months
Health service outcome - referrals to psychiatric services	We will collect relevant health service use data from both intervention arms at 12 months for the previous 12 months. This will include the number of referrals to psychiatric services.	Referrals to psychiatric services at 12 months
Health service outcome - prescriptions for psychotropic medication	We will collect relevant health service use data from both intervention arms at 12 months for the previous 12 months. This will include the number of prescriptions for psychotropic medication	Prescriptions for psychotropic medication at 12 months

Collaborators and Investigators

• Sponsor: University College, London
• Collaborators: National Institute for Health Research, United Kingdom; NHS Health Technology Assessment Programme
• Investigators: Principal Investigator: Marta Buszewicz, University College, London

Study record dates

Study Major Dates

• Study Start: August 1, 2014
• Primary Completion (ACTUAL): February 1, 2016
• Study Completion (ACTUAL): February 1, 2016

Study Registration Dates

• First Submitted: January 16, 2015
• First Submitted That Met QC Criteria: January 26, 2015
• First Posted (ESTIMATE): January 27, 2015

Study Record Updates

• Last Update Posted (ESTIMATE): July 11, 2016
• Last Update Submitted That Met QC Criteria: July 8, 2016
• Last Verified: July 1, 2016

More Information

Terms related to this study

• Keywords: Sertraline; Cognitive Behavioural Therapy (CBT); Selective Serotonin Reuptake Inhibitor (SSRI); Increasing Access to Psychological Therapies (IAPT)
• Additional Relevant MeSH Terms: Mental Disorders; Anxiety Disorders; Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Psychotropic Drugs; Serotonin Uptake Inhibitors; Neurotransmitter Uptake Inhibitors; Membrane Transport Modulators; Serotonin Agents; Antidepressive Agents; Sertraline
• Other Study ID Numbers: 14/0249

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED
• IPD Plan Description: To be discussed and decided by the Data Monitoring Committee