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Behavioural interventions to treat anxiety in adults with autism and moderate to severe intellectual disabilities

Behavioural interventions to treat anxiety in adults with autism and moderate to severe intellectual disabilities (BEAMS-ID)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12637590
Enrollment
80
Registered
2021-02-11
Start date
2021-09-01
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Anxiety in adults with autism and moderate to severe intellectual disabilities Mental and Behavioural Disorders

Interventions

Phase 1a (Intervention Adaptation) The researchers will establish an Intervention Adaptation Group (IAG) comprised of 6 to 8 key stakeholders who will be representatives from their PPI partners, carer

Sponsors

Coventry and Warwickshire Partnership NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Phase 2: 1. Diagnosis of ASD confirmed by case note review 2. Existing diagnosis of moderate to severe intellectual disabilities, confirmed at screening 3. Existing diagnosis of an anxiety disorder confirmed or initially made at screening 4. Carer or family member able to support participation in the intervention (assuming this is one of the key adaptations incorporated) 5. For those who do not have capacity, permission for inclusion in accordance with the Mental Capacity Act (2005)

Exclusion criteria

Exclusion criteria: Phase 2: 1. Currently receiving another psychological therapy for a mental health problem

Design outcomes

Primary

MeasureTime frame
1. Accrual rate recorded as the number of eligible participants who consent to participate in the study per month over 5 months 2. Attrition rate recorded as the number of participants who consent to participate that remain in the study until the end of follow up 3. Response rate recorded as the number of completed assessments per measure at baseline and follow up (within 4 weeks of completion of the intervention) 4. Therapist adherence to the intervention manual measured with fidelity ratings after each treatment session 5. Acceptability of the intervention and associated study procedures to carers and/or participants assessed using semi-structured interviews after the intervention is complete

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 5, 2026