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PsychosisCCP RCTNCT07245212

Testing the Efficacy of the Cannabis Clinic for Patients With Psychosis (CCP) Intervention for Cannabis Use Reduction/Cessation in Patients With First Episode Psychosis (FEP)

A study testing CCP Intervention in people with Psychosis and Cannabis Use Disorder, run by King's College London at 1 site in United Kingdom.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

People suffering from psychosis who use cannabis experience more relapses, long and compulsory admissions, with huge costs to the individual, families and health services. The Cannabis Clinic for Psychosis (CCP) was developed to respond to this clinical need. Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
CCP Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteUnited Kingdom
Study dates
1 Dec 2025to 30 Nov 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • First episode psychosis Community Mental Health teams receiving care under of SLaM Early Intervention for Psychosis Adult Mental Health Teams
  • CUDIT≥9 (Dependent on Cannabis)
  • age=18 to 65 years old ( age range of adult psychiatric services)
  • Capacity to give informed consent, as assessed by clinical teams

Who cannot join

  • Lack capacity to consent
  • High levels of suicidal ideation, judged by clinical team
  • -≥2 days/week frequency use of any other illicit drug
  • Participation in any other current intervention trial
  • In active crises and/or expressing suicidal ideations

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United Kingdom1 site
  • Marina House

    London, SE5 8RZ

    Marta Di Forti, +44 7970211938, marta.diforti@kcl.ac.uk

Other trials in United Kingdom

About this study

Official title: Testing the Efficacy of the Cannabis Clinic for Patients With Psychosis (CCP) Intervention for Cannabis Use Reduction/Cessation in Patients With First Episode Psychosis

People suffering from psychosis who use cannabis experience more relapses, long and compulsory admissions, with huge costs to the individual, families and health services. The Cannabis Clinic for Psychosis (CCP) was developed to respond to this clinical need. A published review of the CCP's intervention showed its safety and efficacy in supporting people suffering from psychosis with reducing their cannabis use. Nevertheless, for the CCP model of care to be applied widely and benefit a larger clinical population, its intervention needs to be tested in a Randomised Control Trial (RCT). The proposed CCP RCT is a waiting list randomised controlled trial that aims to evaluate the clinical efficacy of the existing CCP intervention. Participants will be adults currently under the care of South London and Maudsley (SLaM) Early Intervention Teams for first onset psychosis, who are dependent on cannabis and who express an intention to reduce or stop their use. The RCT primary outcome will measure changes in all participants' cannabis use. Participants will be randomised to either the intervention group or the waiting list control group receiving Treatment As Usual (TAU). The CCP intervention comprises 12 weekly (+/- 4 weeks) one-to-one sessions, with optional participation in a weekly online peer group. Sessions are delivered by trained clinicians and include evidence-based psychosocial techniques, including Motivational Interviewing (MI), Cognitive Behavioural Therapy (CBT), SMART goal settings and support for co-occurring tobacco use. The treatment is non-pharmacological and administered via participant-led approach that accommodates online or face-to-face sessions to meet the patient preference. Qualitative data from the recent CCP proof of concept paper indicate that the flexibility in allowing patients choice on the session's modality (online/face to face, hybrid) increased and maintained engagement.

The study is fully funded by the Maudsley Charity and due to last 30 months from the start of recruitment.

Read the detailed description

Schizophrenia and other psychotic disorders are major causes of chronic ill health and early death. Daily use of high-potency cannabis significantly increases the risk of developing these disorders - up to ninefold - and also worsens outcomes and cognitive function. In the UK, it is estimated that 30-50% of patients presenting with their first episode of psychosis have been using cannabis. Approximately half of these patients continue using cannabis, and those who do are more likely to relapse, experience compulsory and longer admission hospital admissions, and experience more pronounced cognitive effects compared to those who abstain. Regardless of the clear need, there are currently few targeted interventions designed to support individuals with psychosis dependent on cannabis.

To address this urgent gap, in 2019, the first Cannabis Clinic for Psychosis (CCP) was created in the South London and Maudsley NHS Foundation Trust (SLaM) (CCP; maudsleycharity.org/case-studies/cannabis-clinic/). Cannabis use is the most modifiable risk factor for poor clinical outcomes in psychosis with strong evidence linking it to earlier illness onset, more severe symptoms and increased rates of relapse and hospitalisation. Often this population fall into two services: general adult psychiatric services or services for addiction with neither offering an intervention that addresses cannabis use directly. Despite the evidence of cannabis use having a severe impact on the outcome of people navigating psychotic disorders, there is still a lack of treatment available.

Although problematic cannabis use is becoming a significant clinical concern especially among patients with psychosis, there are currently no established treatment guidelines for this clinical population. Currently, the NICE guideline for psychosis recommends a combination of antipsychotics and general management of substance misuse, without specifically addressing the frequent co-morbidity with cannabis use disorder. This underscores a critical gap in care for individuals with psychotic disorders who are actively using cannabis while experiencing their first onset psychosis. In her Independent Review of Drugs, Professor Dame Carol Black recommended that individuals with cooccurring mental health and substance use disorders should receive integrated, concurrent treatment for both conditions. The CCP intervention offers this.

The proposed study is a waiting list randomised controlled trial (RCT) that aims to evaluate the clinical efficacy of the CCP intervention. Participants (n=80) will be adults (aged 18 and over) currently under the care of SLaM Early Intervention Teams for first onset psychosis, who are dependent on cannabis (CUDIT-R score =>9) and express an intention to reduce or stop their use. They will be randomised to either the intervention group (n=40) or the waiting list control group receiving Treatment As Usual (TAU) (N=40). The intervention comprises 12 weekly (+/- 4 weeks) one-to-one sessions, each lasting up to 60 minutes with optional participation in a weekly online peer group based on the CCP recently published proof of concept paper (POC). Sessions are delivered by trained clinicians and include evidence-based psychosocial techniques, including Motivational Interviewing (MI), Cognitive Behavioural Therapy (CBT), and personalised support for co-occurring tobacco use. The treatment is non-pharmacological and administered via participant-led approach that accommodates online or face-to-face sessions to meet the patient preference. Qualitative data from the recent CCP POC paper indicate that the flexibility in allowing patients choice on the session's modality (online/face to face, hybrid) increased and maintained engagement.

The CCP RCT primary outcome will measure, in all participants, changes in the Cannabis Use Disorders Identification Test-Revised (CUDIT-R) score between baseline (before randomisation) and at post-intervention T1 16 weeks after baseline. Other cannabis measures data will be collected at the same time points to assess pattern of use. Secondary outcomes include changes in psychosis symptoms dimensions, paranoia, depression, anxiety, cognitive and overall functioning. Previous findings from the POC analyses of the CCP intervention showed that the CUDIT-R scores, measure of Cannabis Dependence dropped from a baseline mean score 17.88 (5.15), well above the threshold for dependence (=>9) to a post intervention mean score 1.20 (2.10). 74% of participants achieved abstinence, with significant improvements across all secondary outcomes and over 90% returning to work or education. Therefore, the proposed RCT aims to formally test both the efficacy and the safety of the CCP intervention compared to a control group. Data from the CCP POC paper support an expected low risk posed to participants since the intervention is psychosocial in nature and aligned with standard care practices.

Being tested
CCP Intervention
Keywords
Cannabis Use Disorder, Psychosis, First Episode Psychosis, Cannabis Cessation, Cannabis, Reduction, Cessation, Psychosocial Intervention, Psychosocial, Intervention, Cognitive Behavioural Therapy, Motivational Interviewing, Randomised Controlled Trial, Early Intervention in Psychosis, Cannabis Clinic for Psychosis, psychoeducation, peer support, flexibility, personalised
Medical subject headings
Psychotic Disorders, Marijuana Abuse

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CCP InterventionOther

    Also called psychosocial intervention, motivational interviewing, cognitive behavioral therapy

    1. one-to-one weekly sessions: offered both face to face and online to meet the patient preference. Patients can change the meeting modality at any point to suit their needs (e.g. transport difficulties, family commitments, or mental state). The CCP intervention uses a combination of evidence-based psychosocial interventions (PSIs) tailored to each patient's needs. Patients are offered on average 12 (SD 4.2) weeks sessions, for a maximum of 60 minutes.
    2. an online PEER group is facilitated by a senior member of CCP staff and moderated by two PEER mentors with lived experience of psychosis and cannabis use.
Study groups in NCT07245212
Study groupRoleWhat they receive
Cannabis for Psychosis Intervention + Treatment as UsualExperimentalThe CCP intervention consists of two main components: 1. one-to-one weekly sessions: offered both face to face and online to meet the patient preference. Patients can change the meeting modality at any point to suit their needs (e.g. transport difficulties, family commitments, or mental state). The CCP intervention uses a combination of evidence-based psychosocial interventions (PSIs) tailored to each patient's needs. Patients are offered on average 12 (SD 4.2) weeks sessions, for a maximum of 60 minutes 2. an online PEER group is facilitated by a senior member of CCP staff and moderated by two PEER mentors with lived experience of psychosis and cannabis use.
Receives: Other: CCP Intervention
Treatment as Usual / Waiting ListNo interventionParticipants continue Treatment as Usual from their clinical team while on a 16-week waiting list for the CCP intervention.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cannabis Use Disorders Identification Test-Revised score (CUDIT-R)

    The CUDIT-R is an 8-item self-report tool used to screen for cannabis use and cannabis use disorder. Items assess frequency and dependence. Scores range from 0-32, with higher scores indicating greater risk.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

Secondary outcomes (14)
  1. Revised Cannabis Experience Questionnaire (CEQ-mv) combined with the Enhanced cannabis timeline follow back (EC-TLFB)

    Self-report to assess retrospective daily cannabis use, recording weekly THC consumption in standardised units based on frequency, quantity, and potency, age of onset, potency, type, experiences and subjective effects of cannabis.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  2. Psychotic Symptom Rating Scales Delusions Subscale (PSYRATS DEL)

    6-item scale designed to assess different dimensions of delusions with higher scores indicating greater symptom severity.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  3. State Social Paranoia Scale (SSPS)

    10-item measure of recent paranoid thinking in a social situation with higher scores indicating greater levels of paranoia .

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  4. Patient Health Questionnaire-9 (PHQ-9)

    9-item measure that assesses recent levels of depression, with higher scores indicating greater levels of depression.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  5. Generalized Anxiety Disorder-7 (GAD-7)

    7-item measure of assessing recent levels of anxiety, with higher scores indicating greater levels of anxiety.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  6. Changes in the level of social activities (binary measure)

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  7. World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)

    Measures 6 domains of functioning including: cognition, mobility, self-care, getting along, life activities, participation in community

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  8. Global Assessment of Functioning (GAF)

    Using a scale ranging from 0 to 100, with high scores indicating no symptoms and low scores indicating impairment assessing an individual's overall psychological, social, and occupational functioning.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  9. Days in hospital (clinical records)

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  10. Cannabis Withdrawal Scale (CWS)

    Assesses the severity of withdrawal symptoms experienced by individuals after reducing or stopping cannabis use.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  11. Sociodemographic Schedule

    Includes age, gender, sex at birth, ethnicity, education, employment, marital status, living arrangements, and income source

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  12. Qualitative Questionnaire

    Assess feasibility, acceptability, and perceived impact of the CCP intervention, including barriers and facilitators to participant engagement.

    Measured: Measured 16 weeks post-randomisation

  13. Addenbrooke's Cognitive Examination (ACE)

    Cognitive screening tool that assesses attention, memory, language, verbal fluency, and visuospatial skills, with lower scores indicating greater cognitive impairment.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

  14. Fagerström Test for Nicotine Dependence (FTND)

    6-item questionnaire that measures the severity of nicotine dependence, with higher scores indicating stronger physical addiction to nicotine.

    Measured: Measured at a baseline assessment and 16 weeks post-randomisation.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Nov 2025
  2. Study start1 Dec 2025 (estimated)
  3. Primary completion30 Nov 2028 (estimated)
  4. Study completion30 Nov 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Waiting list single-blind RCT
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07245212
Sponsor's protocol ID
361577
Acronym
CCP RCT
Status last verified
Sep 2025
First submitted
13 Nov 2025
Last updated
24 Nov 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Schoeler T, Monk A, Sami MB, Klamerus E, Foglia E, Brown R, Camuri G, Altamura AC, Murray R, Bhattacharyya S. Continued versus discontinued cannabis use in patients with psychosis: a systematic review and meta-analysis. Lancet Psychiatry. 2016 Mar;3(3):215-25. doi: 10.1016/S2215-0366(15)00363-6. Epub 2016 Jan 15.

    PubMed 26777297
  • Patel R, Wilson R, Jackson R, Ball M, Shetty H, Broadbent M, Stewart R, McGuire P, Bhattacharyya S. Association of cannabis use with hospital admission and antipsychotic treatment failure in first episode psychosis: an observational study. BMJ Open. 2016 Mar 3;6(3):e009888. doi: 10.1136/bmjopen-2015-009888.

    PubMed 26940105
  • Di Forti M, Marconi A, Carra E, Fraietta S, Trotta A, Bonomo M, Bianconi F, Gardner-Sood P, O'Connor J, Russo M, Stilo SA, Marques TR, Mondelli V, Dazzan P, Pariante C, David AS, Gaughran F, Atakan Z, Iyegbe C, Powell J, Morgan C, Lynskey M, Murray RM. Proportion of patients in south London with first-episode psychosis attributable to use of high potency cannabis: a case-control study. Lancet Psychiatry. 2015 Mar;2(3):233-8. doi: 10.1016/S2215-0366(14)00117-5. Epub 2015 Feb 25.

    PubMed 26359901
  • Di Forti M, Bond BW, Spinazzola E, Trotta G, Lynn J, Malkin R, Kamran Siddiqui N, Demir S, Opadokun T, Leung PBM, Li Z, Quattrone A, Baxter G, Appiah-Kusi E, Freeman TP, Walsh H, Squeri T, Semikina D, Amberson-Jones F, Austin-Zimmerman I, Meynen T, Quattrone D, Murray RM. A proof-of-concept analysis of data from the first NHS clinic for young adults with comorbid cannabis use and psychotic disorders. BJPsych Open. 2024 Dec 12;11(1):e1. doi: 10.1192/bjo.2024.782.

    PubMed 39663754

Questions about this trial

What is this clinical trial studying?

A study testing CCP Intervention in people with Psychosis and Cannabis Use Disorder, run by King's College London at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 24 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cannabis Use Disorders Identification Test-Revised score (CUDIT-R) (time frame: Measured at a baseline assessment and 16 weeks post-randomisation.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07245212, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Nov 2025.

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