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Accelerating delivery of psychological therapies after stroke

Accelerating Delivery Of Psychological Therapies after Stroke (ADOPTS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12868810
Enrollment
608
Registered
2016-02-04
Start date
2015-11-04
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Topic: Stroke

Interventions

At the start of the study, stroke survivors are interviewed in order to find out about their experience and views of psychological services. In addition, staff at stroke services and psychological ser

Sponsors

University of Central Lancashire
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Case note review All stroke patients on the acute stroke unit will be identified over one week during the usual care period (prior to process mapping and development of the implementation package), and one week during the period of rolling out the implementation package. Main Trial Consecutive stroke patients admitted to the acute stroke units will be identified who: 1. Survive to day 3 post-stroke or being discharged prior to day 3 2. Lives within catchment area of trust 3. Aged 18 or over Process Evaluation Stroke patients and carers Stroke patients and carers will be purposely selected (12 per site) to recruit a balance in sex, age (younger and older), stroke severity (mild, moderate and severe), communication abilities and time since stroke. Staff Staff working within the stroke hospital settings within each of the sites. This may include nurses, doctors, OTs, physiotherapists, allied health professionals, reflecting the range of staff involved in the care pathway at each site.

Exclusion criteria

Exclusion criteria: The participant exclusion criteria is the same for all three elements (casenote review, main trial and process evaluation) and are as follows: 1. Living outside area catchment area of trust 2. Aged under 18 3. Lacks capacity AND has no friend/relative/carer

Design outcomes

Primary

MeasureTime frame
Patient Health Questionnaire 9 item (PHQ-9) at baseline, 6 weeks and 6 months.

Secondary

MeasureTime frame
1. Behavioual Outcomes of Anxiety Scale (BOA) at baseline, 6 weeks and 6 months 2. Generalised Anxiety Disorder 7 item (GAD-7) at baseline, 6 weeks and 6 months 3. Impact of Events Scale 6-items at 6 weeks and 6 months 4. Stroke Aphasia Depression Questionnaire 10 item (SADQ-10) at baseline, 6 weeks and 6 months 5. Work and Social Adjustment Scale 5-items at 6 weeks and 6 months

Countries

England, United Kingdom

Contacts

Public ContactElizabeth Lightbody

Outcome results

None listed

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