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Effectiveness of CAT-GSH for Returning Patients

Effectiveness and Acceptability of Cognitive Analytic Therapy Guided Self-help (CAT-GSH) for Anxiety and Depression for Returning Patients in NHS Talking Therapies Services

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06806176
Enrollment
100
Registered
2025-02-03
Start date
2025-07-30
Completion date
2025-12-31
Last updated
2025-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression

Keywords

Cognitive analytic therapy (CAT), Guided self-help, NHS Talking Therapies, returning patients, Anxiety, Depression

Brief summary

The goal of this clinical trial is to learn if cognitive analytic therapy-guided self-help (CAT-GSH) is comparable to cognitive behavioural therapy-guided self-help (CBT-GSH) in terms of whether it is effective and acceptable for people with anxiety or low mood, who are returning to NHS Talking Therapy services for further treatment. The main questions it aims to answer are: * Does CAT-GSH work well and feel acceptable for people coming back to the Talking Therapies service, compared to CBT-GSH, when taking their characteristics (like age) into account * Does CAT-GSH work well and feel acceptable for people coming back to the Talking Therapies service, compared to those using CBT-GSH for the first time, when taking their characteristics (like age) into account? Participants will: * Choose their preferred treatment * Complete 6 sessions of either CAT-GSH or CBT-GSH * Sessions will be weekly or bi-weekly * Complete routine outcome measures before, during and at the end of therapy

Detailed description

A prospective quantitative, quasi-experimental design will be used to address the primary and secondary questions. PWPs will be trained in delivering CAT-GSH. Participants will choose between CAT-GSH and CBT-GSH and be offered a six-session contact of one-to-one GSH. The Talking Therapies service already collects routine outcome measures, which will be collated and analysed. Procedure/Intervention The Talking Therapies services routinely perform an initial assessment when someone is referred to their services. Potential participants who meet the inclusion criteria will be identified at the assessment stage. Tameside and Glossop Talking Therapies service procedure: The assessor will ask if there is potential interest in a study using a screening script; if the person remains interested, the participant information sheet (PIS) and the consent form will be emailed or posted. At least 48 hours will be left to allow the participant to read the information. The principal investigator will give a follow-up phone call to answer any potential questions, ask for preference on the therapy, and complete the consent form, which will be emailed or posted back to the Talking Therapies service once completed. The completed consent form will be saved in the site's local file and a copy of the form will be sent to the participant. If the person no longer wants to participate at this stage, the service user will receive the treatment as usual. Leeds Mental Wellbeing Service procedure: The assessor will ask if there is potential interest in a study using a screening script; if the person remains interested, the potential participant information sheet (PIS) and the consent form will be emailed or posted. The potential participant will be given 7 days to read the information, email the Leeds service with their preferred treatment, and return the signed consent form to the service if the potential participant does not request further information. 14 days will be given if the participant asks for the material to be posted. If the potential participant requests further information, the clinical lead and principal investigator will contact the potential participant to discuss this. The completed consent form will be saved in the site's local file and a copy will be sent to the participant. If the person no longer wants to participate at this stage or has not emailed within 7 days or returned the forms by post within 14 days, the service user will receive the treatment as usual, so there are no delays. All services procedure: The Talking Therapies services collect routine outcome measures, demographics and other data as standard. Sessions can take place face-to-face, online, or by telephone. The sessions last 35 minutes, for a total of six sessions. Sessions are carried out weekly or bi-weekly. The psychological wellbeing practitioner (PWP) will record the third session with the participant, so the research team can perform a randomly selected competency check on the CBT-GSH and CAT-GSH delivered to service users. The recording will be sent to the research team, with no personally identifiable information on the file name. However, due to the nature of recordings, they may contain identifiable information. Participants will be made aware of this in the PIS. The analysis stage will aim to start in December 2025, to explore the outcome measure data.

Interventions

BEHAVIORALCognitive analytic therapy guided self-help (CAT-GSH)

Six session CAT-GSH treatment

BEHAVIORALCognitive behavioural therapy guided self-help (CBT-GSH)

Six session CBT-GSH treatment

Sponsors

Catalyse CAT Limited
CollaboratorUNKNOWN
Tameside and Glossop Talking Therapies service
CollaboratorUNKNOWN
Leeds Mental Wellbeing service
CollaboratorUNKNOWN
University of Sheffield
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will have a choice between CBT guided self-help and CAT guided self-help.

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Previously received CBT-GSH at same participating NHS Talking Therapies service * Presenting with anxiety or depression * Deemed suitable for step 2 low-intensity therapy, through assessment by a qualified PWP

Exclusion criteria

* Previously received high-intensity therapy since receiving CBT-GSH * The previous treatment episode was in another NHS Talking Therapies service. * Not fluent in English Individuals who are not fluent in English will be excluded from the study due to not having translated CAT-GSH workbooks available and limited funding to translate any workbooks.

Design outcomes

Primary

MeasureTime frameDescription
Composite score (Generalised Anxiety Disorder-7 (GAD-7), Patient health Questionaire-9 (PHQ-9) and Work and Social Adjustment Scale (WSAS))From enrolment to the end of treatment after 6 sessions, weekly or bi-weekly. 6-12 weeks.Routine outcome measures, Generalised Anxiety Disorder-7 (GAD-7), Patient Health Questionaire-9 (PHQ-9) and Work and Social Adjustment Scale (WSAS) collected before, during and after treatment will be combined into composite scores.

Secondary

MeasureTime frameDescription
Patient Health Questionnaire (PHQ-9)From enrolment to the end of treatment at 6-12 weeks. Sessions weekly or bi-weekly.Routine outcome measure, collected as part of normal treatment at the NHS Talking Therapy site - Patient Health Questionnaire-9 (PHQ-9). Collected before, during and after treatment. The PHQ-9 uses a 9-item scale with a total severity score of 0-27. Higher scores indicate greater depression and the clinical cut-off point indicating significant depression is ≥10.
Generalised Anxiety Disorder (GAD-7)From enrolment to the end of treatment at 6-12 weeks. Sessions weekly or bi-weekly.Routine outcome measure, collected as part of normal treatment at the NHS Talking Therapy site - Generalised Anxiety Disorder-7 (GAD-7). Collected before, during and after treatment. The GAD-7 uses a 7-item scale with a total severity score ranging from 0 to 21. Higher scores indicate greater anxiety and the clinical cut-off indicating significant anxiety is ≥8

Countries

United Kingdom

Contacts

Primary ContactAndrew J Laphan
alaphan1@sheffield.ac.uk01142226650
Backup ContactAmrit Sinha
a.sinha@sheffield.ac.uk01142226650

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026