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Narrative Exposure Therapy for Adults With an Intellectual Disability

Acceptability and Feasibility of an Adapted Narrative Exposure Therapy (NET) Protocol for Individuals With an Intellectual Disability

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06934109
Enrollment
13
Registered
2025-04-18
Start date
2024-12-03
Completion date
2026-03-31
Last updated
2026-04-29

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

Conditions

Intellectual Disability, Mild, Learning Disability, PTSD, Trauma, Psychological

Brief summary

The goal of this naturalistic single case series design is to investigate if an adapted Narrative Exposure Therapy protocol can be effective, is feasible, and acceptable for adults with a mile learning disability. Participants will be complete three baseline sessions before taking part in Narrative Exposure Therapy using a manual that has been adapted for people with a learning disability. Trauma symptoms will be measured weekly using the Impact of Events scale adapted for intellectual disabilities. The person's carer will also complete an informant scale related to these symptoms (LANTS-IV). The client will also complete the CORE-LD at pre, and post therapy. Six weeks after the end of the intervention, the client and their carer will be invited to a feedback session to talk about how they found the intervention.

Interventions

NET is a psychological talking therapy that has been designed for people who have experienced multiple and prolonged traumatic experiences. It is typically 12-sessions, involving first a psychoeducation session, then laying a lifeline where stones are lain to represent traumatic events, and flowers positive life events. The following sessions the person is asked to talk through their life, going into detail on the traumatic memories that they have experienced.

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Age 18 and over * Meet the criteria for having a mild ID as assessed by a clinical psychologist within the team * English speaking * Have capacity to consent * The participant must be experiencing trauma related stress as assessed by themselves, the clinical psychologist and the research team * Be able to travel to one of the therapy sites * Carer participant must have ability to reflect and comment on the trauma related stress experienced by the client participant * Carer must also be 18 years old or older and be English speaking. * Carer must have known participant for 1 year or more.

Exclusion criteria

* They are substance dependent * They are currently receiving another trauma-focused intervention * Currently an inpatient * Carers excluded if they lack capacity to consent to take part in research

Design outcomes

Primary

MeasureTime frameDescription
Impact of Events Scale for intellectual disabilities (IES-ID)Completed weekly through baseline and intervention stages, approximately 16 weeks. Then at 6-week follow up (approximately week 22).The IES-ID (Hall et al., 2014) is a 22 item scale scored on a three-point Likert scale measuring trauma related symptoms. This is an adapted measure that has been validated for people with an intellectual disability.
Lancaster and Northgate Trauma Scale for Intellectual Disabilities - Informant Version (LANTS-IV; Wigham et al., 2011)Completed weekly through baseline and intervention stages, approximately 16 weeks. Then at 6-week follow up (approximately week 22).47 scored on a six-point scale for frequency and three-point for severity.
Clinical Outcome Routine Evaluation-Learning Disabilities (CORE-LD; Brooks et al., 2013)At baseline week 1 and at 6-week follow-up (approximately week 22).14 scored on a three-point Likert scale measuring psychological distress across four domains: well-being, symptoms, functioning, and risk
Change interview (Elliott et al., 2001) with clients and carers6-weeks post-intervention. Sessions will be around 30-60 minutes.A feedback session will be held with the client and their carer around 6-weeks after the therapy has come to an end. This will ask for feedback on how they found the intervention.

Secondary

MeasureTime frameDescription
Heart rateWeekly during the intervention sessions, for approximately 12-weeks.Heart rate will be taken using a fitness watch that can measure continuous heart rate. This will show whether any within and between session habituation has taken place. Subjective units of distress (Wolpe, 1969) will be used if clients do not wish to wear a heart rate device.
Post-session therapist reflectionsAcross the intervention phase, an average of a yearTherapist reflections will be collected to gather information about their thoughts relating to the manual and therapy.

Countries

United Kingdom

Contacts

PRINCIPAL_INVESTIGATORThomas Schroder

University of Nottingham

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026