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Developing a service in community pharmacies to increase earlier identification of alcohol-related liver disease

Community pharmacy alcohol-related liver disease risk identification and linkage to care through development of a complex intervention (CIPLINC) study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN12116769
Enrollment
26
Registered
2022-10-26
Start date
2022-10-01
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Alcohol-related liver disease Digestive System

Interventions

The community pharmacy alcohol-related liver disease (ArLD) risk identification and linkage to care through development of a complex intervention, or ‘CIPLINC’, study will use the structure of the Med

Sponsors

University of Southampton
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All participants: 1. Age 18 years or over 2. Able to give written consent in English Specific to participant groups: Group 1 - Patients with Alcohol-related liver disease (ArLD) 1. Diagnosis of ArLD 2. Under the care of gastroenterology/hepatology outpatient clinic Group 2 - Community Pharmacy users 1. Attended a community pharmacy at least once in the last year 2. Drink alcohol 3. Offered novel service* 4. Engaging with novel service*# Group 3 - Community Pharmacy staff 1. Currently working in a community pharmacy as pharmacist, pharmacy assistant or pharmacy technician 2. Member of staff in a pharmacy delivering the novel service* Group 4 - Healthcare professional involved in ArLD Care Pathways Currently employed as any of: 1. General Practitioner 2. Primary care nurse practitioner 3. Hepatology consultant 4. Hepatology specialist nurse 5. Alcohol care team worker *only applies to participants being recruited after implementation of the novel service #requirement for participants for telephone surveys only

Exclusion criteria

Exclusion criteria: All participants: 1. Age <18 years 2. Unable to understand written and spoken English to consent for or complete the study 3. Lacking capacity to consent Specific to participant groups: Group 2 Community Pharmacy users 1. Currently working as a member of pharmacy team (pharmacist, pharmacy technician, pharmacy support staff) 2. Current healthcare professional involved in ArLD Care Pathways Group 3 Community Pharmacy staff 1. Member of staff not involved in delivering the novel service* *only applies to participants being recruited after implementation of the novel service

Design outcomes

Primary

MeasureTime frame
1. Pharmacy recruitment rate recorded as the number of eligible pharmacies recruited to deliver the novel service. Timepoint 31/09/2024 2. Acceptability of the novel service to service providers and service users measured using qualitative interviews. Timepoint 31/03/2025 3. Feasibility of implementing the novel service measured by analysis of service use data. Timepoint 31/03/2025

Secondary

MeasureTime frame
1. Number of people assessed in the service measured from service use data. Timepoint 31/03/2025 2. Number of people assessed in the service identified as at risk of alcohol related liver disease measured from service use data. Timepoint 31/03/2025 3. Number of people identified in the service as at risk of alcohol related liver disease connected to alcohol related liver disease pathways of care measured from service use data. Timepoint 31/03/2025 4. Recruitment rate of telephone survey recorded as the number of eligible participants who consent to participate in the telephone survey. Timepoint 31/03/2025

Countries

England, United Kingdom

Outcome results

None listed

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