search
Back to results

Testing and Treating Hepatitis C in Community Pharmacies (SuperDOT-C)

Primary Purpose

Hepatitis C

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Pharmacist Led
Nurse led
Sponsored by
University of Dundee
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Hepatitis C

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • HCV PCR positive,
  • Stable OST dose for greater than 12 weeks prior to study enrolment

Exclusion Criteria:

  • Evidence of current or previous decompensated liver disease,
  • Currently receiving HCV eradication treatment
  • HIV infection,
  • HBsAg positive with detectable HBV DNA,
  • Pregnancy
  • Cirrhosis or high fibrosis score
  • Genotype deemed unsuitable for treatment with available study drugs
  • Unable or unwilling to provide informed consent

Sites / Locations

  • NHS Grampian
  • NHS Tayside
  • NHS Greater Glasgow and Clyde

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Pharmacist Led

Nurse Led

Arm Description

This arm involved subjects following pathway of care and treatment delivery delivered by community pharmacists

This arm involved subjects following the conventional pathway of care and treatment delivery delivered by specialist secondary care nurses

Outcomes

Primary Outcome Measures

Rate of Sustained Viral Response at 12 weeks, (SVR12), in pharmacy pathway compared with that of the current treatment pathway 12 weeks after completion of HCV therapy
Blood test result; PCR - based measurement of levels of hepatitis C virus.

Secondary Outcome Measures

Cost effectiveness of the pharmacist pathway as compared with the conventional care pathway
Health economics analysis
To determine whether the Pharmacist-led pathway compared with the Conventional Pathway leads to more people on OST being tested and initiating treatment
Comparison of rate of HCV testing rates in pharmacist pathway compared with current pathway
To explore whether adherence and persistence to HCV therapy in the pharmacy setting is at least similar to that in the Conventional pathway
Comparison of compliance rates of antiviral medications between pharmacist and conventional pathway.
To compare the acceptability of the Pharmacist-led pathway versus the conventional treatment pathway for OST clients
Compare the acceptability of the pharmacist pathway as compare to conventional pathway of care
To measure re-infection rate at 1 year after end of treatment in patients with SVR
Comparison of the rate of reinfections with HCV between pharmacist and conventional pathways
To compare the number of patients who drop out of the study between the two pathways
Comparison of subject drop out rates between pharmacist and conventional pathways

Full Information

First Posted
March 4, 2016
Last Updated
August 29, 2019
Sponsor
University of Dundee
search

1. Study Identification

Unique Protocol Identification Number
NCT02706223
Brief Title
Testing and Treating Hepatitis C in Community Pharmacies
Acronym
SuperDOT-C
Official Title
A Cluster Randomised Trial of Pharmacy Led HCV Therapy Versus Conventional Treatment Pathways for HCV Positive Patients Receiving Daily OST in Pharmacies in Health Boards Within NHS Scotland
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
December 2016 (Actual)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
March 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Dundee

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hepatitis C Virus, (HCV), infection is a major health concern in the UK with up to 0.7% of the population infected. At best, 25% of those infected will clear the infection spontaneously, though for those who develop a chronic infection, they may go onto to develop liver cirrhosis or liver cancers. The standard of care within the NHS is that patients with a history of intravenous drug use or those currently on methadone are at high risk of having HCV infection and should be offered HCV testing. Once diagnosed they can be referred to nurse led treatment pathways. Less than 10% of the methadone users are even tested for HCV and of them fewer than 20% go onto treatment regimens that successfully clear the infection despite regular interactions with heath care staff. Pharmacists who have daily interactions with patients receiving methadone are ideally placed to deliver anti HCV therapy as they have daily contact with this client group and are well placed to advise on the drug therapy. The SuperDOT C study will examine the impact of pharmacy led Directly Observed Therapy (DOT) for HCV treatment in patients attending Community Pharmacies in participating Health Boards within NHS Scotland. The impact of this approach will be compared with those referred to standard care pathways on how well participants clear their HCV infection.
Detailed Description
The SuperDOT-C study will evaluate a new pathway of care for patients on OST who are already receiving OST therapy on a daily basis from a pharmacist. Newer therapies for HCV have recently become much simpler to initiate and supervise with much improved effectiveness and as described below it is now proposed to extend the role of community pharmacists into initiating HCV therapy alongside the existing OST The SuperDOT-C study will utilise this existing environment and relationship to smooth the pathway into HCV therapy with co-administration of OST alongside the anti-HCV therapy under the supervision of the pharmacist compared with the established pathway of referral to another site and treatment with a nurse led ant-HCV treatment program. This new pathway may have positive effects on the movement towards HCV cure at multiple levels. The planned pathway is different to current care at each point, from testing and diagnosis through adherence to cure. In the planned pathway, the patient interacts with the pharmacist on a daily basis, as compared to intermittent interaction with a secondary care team member. The result being that the patient has a shorter care pathway, with less travelling and better access to anti-HCV treatment. The daily interaction with the pharmacy provides opportunities to assess and support the patient, provide sound advice and care, with the added benefit of being able to directly observe treatment, (DOT), thus potentially improving adherence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
356 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pharmacist Led
Arm Type
Experimental
Arm Description
This arm involved subjects following pathway of care and treatment delivery delivered by community pharmacists
Arm Title
Nurse Led
Arm Type
Experimental
Arm Description
This arm involved subjects following the conventional pathway of care and treatment delivery delivered by specialist secondary care nurses
Intervention Type
Other
Intervention Name(s)
Pharmacist Led
Intervention Description
Trial of administering established, licensed treatments by a novel pathway, ie Community Pharmacists, which is hypothesized to improve treatment and retention in treatment of difficult to engage subjects
Intervention Type
Other
Intervention Name(s)
Nurse led
Intervention Description
Trial of administering established, licensed treatments by the conventional clinical care pathway, ie Specialist nurses
Primary Outcome Measure Information:
Title
Rate of Sustained Viral Response at 12 weeks, (SVR12), in pharmacy pathway compared with that of the current treatment pathway 12 weeks after completion of HCV therapy
Description
Blood test result; PCR - based measurement of levels of hepatitis C virus.
Time Frame
12 week SVR, (12 weeks post completion of HCV treatment)
Secondary Outcome Measure Information:
Title
Cost effectiveness of the pharmacist pathway as compared with the conventional care pathway
Description
Health economics analysis
Time Frame
Span of study ie 24 months
Title
To determine whether the Pharmacist-led pathway compared with the Conventional Pathway leads to more people on OST being tested and initiating treatment
Description
Comparison of rate of HCV testing rates in pharmacist pathway compared with current pathway
Time Frame
Span of study ie 24 months
Title
To explore whether adherence and persistence to HCV therapy in the pharmacy setting is at least similar to that in the Conventional pathway
Description
Comparison of compliance rates of antiviral medications between pharmacist and conventional pathway.
Time Frame
Span of study ie 24 months
Title
To compare the acceptability of the Pharmacist-led pathway versus the conventional treatment pathway for OST clients
Description
Compare the acceptability of the pharmacist pathway as compare to conventional pathway of care
Time Frame
Span of study ie 24 months
Title
To measure re-infection rate at 1 year after end of treatment in patients with SVR
Description
Comparison of the rate of reinfections with HCV between pharmacist and conventional pathways
Time Frame
Span of study ie 24 months
Title
To compare the number of patients who drop out of the study between the two pathways
Description
Comparison of subject drop out rates between pharmacist and conventional pathways
Time Frame
Span of study ie 24 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HCV PCR positive, Stable OST dose for greater than 12 weeks prior to study enrolment Exclusion Criteria: Evidence of current or previous decompensated liver disease, Currently receiving HCV eradication treatment HIV infection, HBsAg positive with detectable HBV DNA, Pregnancy Cirrhosis or high fibrosis score Genotype deemed unsuitable for treatment with available study drugs Unable or unwilling to provide informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John F Dillon, MD
Organizational Affiliation
University of Dundee
Official's Role
Principal Investigator
Facility Information:
Facility Name
NHS Grampian
City
Aberdeen
ZIP/Postal Code
AB25 2ZN
Country
United Kingdom
Facility Name
NHS Tayside
City
Dundee
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
Facility Name
NHS Greater Glasgow and Clyde
City
Glasgow
ZIP/Postal Code
G$ 0SF
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32526210
Citation
Radley A, de Bruin M, Inglis SK, Donnan PT, Hapca A, Barclay ST, Fraser A, Dillon JF. Clinical effectiveness of pharmacist-led versus conventionally delivered antiviral treatment for hepatitis C virus in patients receiving opioid substitution therapy: a pragmatic, cluster-randomised trial. Lancet Gastroenterol Hepatol. 2020 Sep;5(9):809-818. doi: 10.1016/S2468-1253(20)30120-5. Epub 2020 Jun 8.
Results Reference
derived
PubMed Identifier
31551376
Citation
Hickman M, Dillon JF, Elliott L, De Angelis D, Vickerman P, Foster G, Donnan P, Eriksen A, Flowers P, Goldberg D, Hollingworth W, Ijaz S, Liddell D, Mandal S, Martin N, Beer LJZ, Drysdale K, Fraser H, Glass R, Graham L, Gunson RN, Hamilton E, Harris H, Harris M, Harris R, Heinsbroek E, Hope V, Horwood J, Inglis SK, Innes H, Lane A, Meadows J, McAuley A, Metcalfe C, Migchelsen S, Murray A, Myring G, Palmateer NE, Presanis A, Radley A, Ramsay M, Samartsidis P, Simmons R, Sinka K, Vojt G, Ward Z, Whiteley D, Yeung A, Hutchinson SJ. Evaluating the population impact of hepatitis C direct acting antiviral treatment as prevention for people who inject drugs (EPIToPe) - a natural experiment (protocol). BMJ Open. 2019 Sep 24;9(9):e029538. doi: 10.1136/bmjopen-2019-029538.
Results Reference
derived
PubMed Identifier
30552244
Citation
Radley A, de Bruin M, Inglis SK, Donnan PT, Dillon JF. Clinical effectiveness of pharmacy-led versus conventionally delivered antiviral treatment for hepatitis C in patients receiving opioid substitution therapy: a study protocol for a pragmatic cluster randomised trial. BMJ Open. 2018 Dec 14;8(12):e021443. doi: 10.1136/bmjopen-2017-021443.
Results Reference
derived

Learn more about this trial

Testing and Treating Hepatitis C in Community Pharmacies

We'll reach out to this number within 24 hrs