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NCT Number: NCT07143383

CAMHS and Social Prescribing Applications

Background: Social prescribing (SP) is a mechanism for linking patients with non-medical forms of community support and has demonstrated mental health benefits for adults and young people (YP). However, SP is predominantly based in primary care, which limits accessibility for YP who typically engage less with this setting. Within CAMHS (Child and Adolescent Mental Health Services), SP has only recently begun to be trialed, mainly as a pre-treatment option while waiting for care. The CASPA study will pilot a novel SP pathway embedded after the start of psychological treatment in CAMHS, aiming to test its feasibility, acceptability, and potential impact on mental health and wellbeing through a randomized controlled trial.

Methods: CASPA is a two-group (intervention vs. active control) parallel randomized pilot study with YP as the unit of randomization. A total of 120 YP aged 11-18, who have started psychological treatment for emotional difficulties in one of three CAMHS sites in England, will be recruited. Participants in the intervention group will receive a co-produced, person-centered SP pathway involving up to six sessions with a trained Link Worker (LW). These sessions will help identify 'what matters to them' and connect YP with locally mapped community activities and support (e.g. arts, sports, volunteering). Participants in the control group will receive signposting to the same community resources via a leaflet from CAMHS staff or researchers. Quantitative data will be collected at baseline, 3-month and 6-month follow-up, including measures of resilience, mental health, wellbeing, service use, and quality of life. Primary outcomes include feasibility, acceptability, and appropriateness of the intervention, assessed through validated measures and participation metrics, alongside any evidence of impact. Qualitative interviews with YP, CAMHS staff, and LWs will explore implementation experiences, barriers, facilitators, and mechanisms of impact.

Discussion: The CASPA study will generate preliminary evidence regarding the feasibility, acceptability, and appropriateness of offering SP after psychological treatment within CAMHS has started. It will also provide early insights into whether this approach can improve outcomes for YP with emotional difficulties. Findings will inform decisions on the design and justification for a future full-scale clinical and cost-effectiveness trial.

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Key information

Age range

11 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Eligibility criteria

Inclusion criteria

(i) CAMHS

  • Wish to participate in CASPA
  • Located in England

(ii) YP Participants

  • Aged between 11 to 18 years
  • Capacity to give assent (if under 16), or
  • Capacity to give informed consent (if aged 16 or over or has Gillick competence if aged under 16)
  • Have started psychological treatment in CAMHS for an emotional difficulty (e.g. depression, anxiety)

(iii) Parent/Guardian Participants

  • Aged 18 or over
  • Capacity to give informed consent for YP involvement in CASPA (when the YP is aged between 11-15 and lacks Gillick competence)

(iv) CAMHS staff and LWs:

  • Aged 18 or over
  • Capacity to give informed consent to participate in CASPA

Exclusion criteria

(i) YP participants

  • YP with emotional difficulties put on an enhanced specialist pathway due to another severe and complex difficulty which requires intensive input (e.g. anorexia, psychosis or severe and complex difficulties (as judged by the assessing clinician))

Treatment and study plan

Social Prescribing

Behavioral

SP is a person-centered approach to wellbeing involving the co-development of a non-clinical prescription, between an individual (i.e. young person) and Link Workers (LWs), based on the perceived difficulties for the referral and the YPs values, needs and preferences. LWs have a good knowledge of their local areas, via community asset mapping and networking, allowing them to connect individuals with different types of available support and activities. Typically, SP ranges from 6-12 sessions (average 8 sessions: unpublished data from sites) with a LW over an 8-week period. Sessions may take place online, via phone call, or in person. As part of this process, LWs draw on psychological skills such as motivational interviewing and behavioral activation as well as employ problem solving and goal setting. Following the identification of issues and preferences, the LW will discuss with the YP what the available local activities and support structures are that match their preferences.

Signposting

Behavioral

Those in the control group will receive signposting to activities and local sources of support in their communities. This will consist of a CAMHS clinician or researcher meeting with YP identified and providing them with a leaflet detailing the same local sources of support identified by the LW from asset mapping.

Primary outcomes

  1. Acceptability (young people)

    Time frame: 3 and 6 months

    YP: Acceptability will be assessed using an item from the Friends and Family test, which asks individuals to rate how likely they would be to recommend the service (in this instance, the SP pathway). It is assessed on a five-point Likert Scale, ranging from '1' Extremely Unlikely to '5' Extremely Likely. Higher scores indicate better acceptability.

Secondary outcomes

  1. Acceptability (CAMHS Staff and LWs)

    Time frame: 6 months

    Acceptability of Intervention Measure (AIM) is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20)

  2. Feasibility (young people)

    Time frame: Post intervention (t least 3 months)

    YP will be asked about the feasibility of the intervention via qualitative interviewing where questions can be appropriately framed for their age and experience.

  3. Feasibility (CAMHS Staff and LWs)

    Time frame: 6 months

    Description: Link workers (LW) and CAMHS staff: Feasibility of Intervention Measure (FIM) is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher intervention feasibility.

  4. Appropriateness (young people)

    Time frame: 3 and 6 months

    Appropriateness will be assessed by the proportion of sessions offered versus the number the young person attends.

  5. Appropriateness (CAMHS Staff and LWs)

    Time frame: 6 months

    Appropriateness Intervention Appropriateness Measure (IAM) is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher intervention appropriateness

  6. Wellbeing: ONS Personal Wellbeing Questions

    Time frame: Baseline, 3 and 6 months

    The Office for National Statistics ONS3 are three subjective measures designed to capture key aspects of personal well-being in the general population. These questions assess three core domains of well-being: evaluative, eudemonic, and affective. Respondents are asked to rate the three questions on a scale from 0 (not at all) to 10 (completely).

    Higher scores reflect greater well-being

  7. Depression: Short Mood and Feelings Questionnaire.

    Time frame: Baseline, 3 and 6 months

    The SMFQ is a 13-item scale questionnaire. Each item reflects core symptoms of depression based on DSM criteria, such as sadness, tiredness, irritability, and feelings of worthlessness. Respondents rate how true each statement has been over the past two weeks on a 3-point Likert scale: "Not True", "Sometimes True", or "True".

    Higher scores reflect greater levels of depressive traits.

  8. Anxiety: Generalised Anxiety Disorder-7 Questionnaire.

    Time frame: Baseline, 3 and 6 months

    The GAD-7 includes 7 items, each reflecting a DSM-IV symptom of generalized anxiety disorder such as excessive worry, nervousness, and difficulty relaxing. Respondents are asked how often they were bothered by each symptom over the past two weeks, using a 4-point Likert scale ranging from "Not at all" to "Nearly every day." Total scores range from 0 to 21, with cutoff points identifying mild (5), moderate (10), and severe (15) anxiety.

  9. Stress: Perceived Stress Scale-4.

    Time frame: Baseline, 3 and 6 months

    The PSS-4 includes four questions evaluating how unpredictable, uncontrollable, and overloaded individuals find their lives. Responses are given on a 5-point Likert scale ranging from 0 ("Never") to 4 ("Very often"). Higher scores indicate greater perceived stress.

  10. Service Use: Short-Client Service Receipt of Inventory.

    Time frame: Baseline, 3 and 6 months

    The CSRI gathers detailed information on service contacts, informal care, medication use, employment, and accommodation over a specified recall period, in this instance, 3 months.

    The first 9 questions on frequency of healthcare service use are scored on a 6-point Likert scale, ranging from 0 'not at all', to 6 'once per day'. Higher scores indicate more contact with services.

    The next 2 questions explore contact with emergency healthcare services (accident and emergency and inpatient admission' and are scored 1 'no' or 2 'yes'. Higher scores indicate more contact with emergency services. For inpatient admission, patients are also asked to specify the number of days they were in hospital.

    The next question explore the impact and support of mental health on an individual's school or workplace. One question asks how many days were missed at school or the individual's workplace because of mental health difficulties. Scores range from 0-93 with higher scores indicating more days missed

  11. Quality of Life: Child Health Utility-9D.

    Time frame: Baseline, 3 and 6 months

    The Child Health Utility-9D (CHU-9D) was developed to address the lack of generic preference-based measures specifically designed for children. The CHU-9D encompasses both shared and unique dimensions compared to other instruments. Common areas include pain and usual activities, while child-specific dimensions include schoolwork/homework, tiredness, and sleep. CHU9D is assessed using 9 questions on a five-point Likert scale (scoring between 1-5). Higher scores indicate higher quality of life.

Other outcomes

  1. Emotional Regulation: ERICA

    Time frame: Baseline, 3 and 6 months

    Mechanism: ERICA is a 17-item tool explicitly developed for youth and designed to assess emotional self-efficacy and regulation strategies in children aged 8 to 16. Its structure covers emotional self-awareness, emotional control, and situational responsiveness, offering a well-rounded view of emotion regulation capacity. Emotional regulation is assessed using 16 questions each on a five-point Likert scale ('1' Strongly disagree to '5' Strongly agree) including 10 questions being reverse scored.

    Higher scores indicate greater emotional regulation.

  2. Community connection: subscale of Student Resilience Survey

    Time frame: Baseline, 3 and 6 months

    Mechanism: using questions from the Student Resilience Survey which is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher community connection.

  3. Self-esteem: subscale of Student Resilience Survey

    Time frame: Baseline, 3 and 6 months

    Mechanism: using questions from the Student Resilience Survey which is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher self-esteem.

  4. Problem solving: subscale of Student Resilience Survey

    Time frame: Baseline, 3 and 6 months

    Mechanism using the Student Resilience Survey which is assessed using 3 questions each on a five-point Likert scale (scoring between 3-15). Higher scores indicate higher problem solving with others.

  5. Goals and aspirations: subscale of Student Resilience Survey

    Time frame: Baseline, 3 and 6 months

    Mechanism using the Student Resilience Survey which is assessed using 3 questions each on a five-point Likert scale (scoring between 3-15). Higher scores indicate higher levels of goals and aspirations.

  6. Family connection: subscale of Student Resilience Survey

    Time frame: Baseline, 3 and 6 months

    Mechanism: using questions from the Student Resilience Survey which is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher family connection.

  7. School connection: subscale of Student Resilience Survey

    Time frame: Baseline, 3 and 6 months

    Mechanism: using questions from the Student Resilience Survey which is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher school connection.

  8. Social Structure and Quality.

    Time frame: Baseline, 3 and 6 months

    Mechanism: using questions adapted from PISA 2022 and MCS4 which is assessed using five questions. One of which requires an open-ended numerical value and four questions which are rated on a five-point Likert scale (scoring between 0-16). Higher scores indicate a greater social structure and friendship quality.

  9. Therapeutic Alliance

    Time frame: 3 and 6 months

    Mechanism using the Session Feedback Questionnaire which is assessed using 4 questions each on a five-point Likert scale (scoring between 4-20). Higher scores indicate higher therapeutic alliance. This is for individuals in the social prescribing intervention only.

Study contacts

Contact information is provided by the study sponsor or research team.

Daniel Hayes, PhD

CONTACT

[email protected]

07747444010

Robert Booth, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University College, London

Other

Collaborators

  • National Academy for Social Prescribing
  • We Do Wellbeing

Registry information

Acronym: CASPA

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Aug 27, 2025
Registry last updated
Sep 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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