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Enhancing care for delirium in palliative care units

DAMPen-Delirium II: Improving the detection, assessment, management, and prevention of delirium in palliative care units: a cluster randomised-controlled trial, economic analysis and process evaluation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN23678136
Enrollment
2000
Registered
2025-04-16
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-05-19

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

Conditions

Delirium Mental and Behavioural Disorders

Interventions

The DAMPen-Delirium II study has three work packages: 1. Cluster Randomised Controlled Trial (CRCT) This work package will evaluate the effectiveness of CLECC-Pal Delirium vs. usual practice on reduc
mid-shift cluster discussions by the professionals delivering care
peer observations of practice
reflective discussions
and action learning sets (all designed to implement changes in delirium screening, assessment and management). Twenty palliative care units (charitably-funded or NHS) will be randomised (1:1) to the

Sponsors

University of Hull
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inpatients/Carers Inclusion Criteria: 1. Inpatients with capacity to consent 2. Carers of inpatients with capacity to consent

Exclusion criteria

Exclusion criteria: Interview: Inpatients/Carers Exclusion Criteria: 1. Patients who do not have capacity at the point of interview will be withdrawn 2. Carers of inpatients without capacity to consent

Design outcomes

Primary

MeasureTime frame
Primary outcome measures (clinical): The proportion of inpatient days affected by delirium for inpatients who experience delirium during PCU admission, calculated as the number of days they experience delirium (as identified with the Inouye tool by HHTU researchers) divided by their total number of inpatient days, measured using data extracted from patient records at one timepoint

Secondary

MeasureTime frame
Secondary outcomes (process-related and clinical): 1. Guideline adherence: The number of inpatient records that contain the following evidence of adherence to delirium care guidelines (for the detection, assessment, management and prevention of delirium) at baseline and follow-up: 1.1. Use of 4AT screening tool 1.2. Presence/absence of delirium risk assessment 1.3. Use of Richmond Agitation-Sedation Scale-Pal 1.4. Clinician-documented diagnosis of delirium 1.5. Clinician assessment of cause/reversibility 1.6. Presence/absence of delirium care plan 1.7 Use of antipsychotics in relation to documented harmful/distressing behaviour towards self or others 2. Cost-effectiveness: The incremental cost-effectiveness ratio measures the cost per PCU inpatient day saved by preventing delirium, measured using data collection from the cRCT linked with Hospital Episode Statistics (HES) at the end of the study 3. Inpatient Demographics measured using data extracted from patient records at one timepoint: 3.1. Age 3.2. Sex 3.3. Diagnosis 3.4. Ethnicity 3.5. Postcode (converted to IMD score at data collection) 3.6. Primary Medical Condition 3.7. Date of Death (if applicable) 3.8. Length of stay

Countries

England, United Kingdom, Wales

Contacts

Public ContactGrant Constable
grant.constable@hyms.ac.uk+44 (0)1482463732

Outcome results

None listed

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