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Narrative Experiences Online (NEON): impact of recorded mental health recovery stories on quality of life in people experiencing psychosis

The Narrative Experiences Online (NEON) trial: a two-arm randomised controlled trial in which people with experience of psychosis receive access to (arm 1) versus receive one year delayed access to (arm 2) recorded mental health recovery narratives delivered online, with quality of life as a primary outcome, and hope, empowerment, meaning in life and symptomatology as secondary outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11152837
Enrollment
683
Registered
2018-08-13
Start date
2020-03-09
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

Mental health Mental and Behavioural Disorders

Interventions

Current interventions as of 12/11/2019: Equal allocation across arms: Arm 1: treatment as usual plus access to online recovery narratives for one year Arm 2: treatment as usual for one year, followed

Sponsors

Nottinghamshire Healthcare NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 12/11/2019: 1. Experience of psychosis in the last five years 2. Experience of mental health-related distress in the previous 6 months 3. Resident in England 4. Aged 18 years or above 5. Capable of accessing or being supported to access the internet, either on a personal computer, mobile device or at a community venue 6. Able to understand written and spoken English 7. Capable of providing online informed consent 8. Any gender Previous inclusion criteria: 1. Aged 18-65 2. Any gender 3. Primary or secondary clinical diagnosis of psychosis (including e.g. schizophrenia, schizoaffective disorder, bipolar disorder) 4. Currently using mental health services in England 5. Able to understand English 6. Able to access or be supported to access the internet 7. Able to give online informed consent

Exclusion criteria

Exclusion criteria: Does not meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
Current primary outcome measure as of 12/11/2019: Health-related quality of life assessed using the Manchester Short Assessment (MANSA) at 1 week, 12 weeks and 52 weeks (primary endpoint) after baseline Previous primary outcome measure: Health-related quality of life assessed using the Manchester Short Assessment (MANSA) at 1 week, 3 months and 1 year after baseline

Secondary

MeasureTime frame
Current secondary outcome measures as of 12/11/2019: Assessed at 1 week, 12 weeks and 52 weeks after baseline: 1. Hope assessed through the Herth Hope Index (Herth, 1992) 2. Meaning in Life assessed through the Meaning in Life Questionnaire (Steger et al, 2006) 3. Empowerment assessed through the Mental Health Confidence Scale (Carpinello et al, 2000) 4. Symptomatology assessed through CORE-10 (Barkham et al, 2013) Previous secondary outcome measures: Assessed at 1 week, 3 months and 1 year after baseline: 1. Hope assessed through the Herth Hope Index (Herth, 1992) 2. Meaning in life assessed through the Meaning in Life Questionnaire (Steger et al, 2006) 3. Empowerment assessed through the Mental Health Confidence Scale (Carpinello et al, 2000) 4. Symptomatology assessed through a standardised measure (to be determined) 5. Quality of social relationships assessed through a non-standardised scale to be developed within the NEON study

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 26, 2026