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Testing a new intervention for anxiety in people with mild to moderate intellectual disabilities

Testing a Co-designed Mental imagery Anxiety intervention for people with mild to moderate Intellectual Disabilities (Co-MAID)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN70980810
Enrollment
12
Registered
2024-05-10
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

Treatment of clinical levels of anxiety in people with mild to moderate intellectual disabilities Mental and Behavioural Disorders

Interventions

A single case experimental design with a process evaluation will be conducted with 6 individuals to assess the acceptability of the Co-MAID intervention and associated research procedures. Participant

Sponsors

Berkshire Healthcare NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosis of mild or moderate intellectual/ learning disabilities 2. Aged 18 years or older 3. Score of 15 or more on the Glasgow Anxiety Scale 4. Capacity to decide whether they wish to partake in this study

Exclusion criteria

Exclusion criteria: 1. Currently receiving another psychological therapy for a mental health problem 2. Presenting with mental health symptoms of a disorder other than anxiety which are judged likely to interfere with their ability to successfully participate in the intervention by the study team (e.g., hallucinations and delusions or suicidality).

Design outcomes

Primary

MeasureTime frame
Anxiety measures using the Glasgow Anxiety Scale (GAS) at baseline, weeks 5 and 9 of the intervention and 2 weeks follow-up

Secondary

MeasureTime frame
1. Psychological well-being measured using the adapted Patient Health Questionnaire (PHQ-9), Generalised Anxiety Disorder (GAD-7) questionnaire and Psychological Therapies Outcome Scale for people who have Intellectual Disabilities (PTOS-ID) at baseline, weeks 5 and 9 of the intervention and 2 weeks follow-up 2. Mood measured using daily recording that is undertaken throughout the baseline, intervention and follow-up phases in line with the SCED methodology

Countries

England, United Kingdom

Contacts

Public ContactOlivia Hewitt
olivia.hewitt@berkshire.nhs.uk+44 (0)7812512184

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026