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Completion and Acceptability of Treatment Across Primary Care and the commUnity for Latent Tuberculosis (CATAPULT)

Primary Purpose

Latent Tuberculosis

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Community/Primary Care
Hospital/TB Clinic
Sponsored by
Queen Mary University of London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Latent Tuberculosis

Eligibility Criteria

16 Years - 35 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with LTBI aged 16-35 and who have entered the UK less than 5 years ago from a country with a TB incidence of greater than 150/100,000.
  • Latent Tuberculosis is defined as a positive IGRA test without any symptoms or physical signs of active Tuberculosis and no evidence of active Tuberculosis on Chest X-ray.

Exclusion Criteria:

  1. Pregnant or breastfeeding women
  2. Patients requiring medications that cannot be safely taken with Rifinah
  3. HIV infection.
  4. Individuals with known liver disease, or abnormal liver function tests (LFTs)
  5. Diagnosis of cirrhosis (jaundice, haematemesis, ascites or previous episodes of liver encephalopathy)
  6. Chronic or active hepatitis B or hepatitis C virus infection
  7. Previous treatment for TB or LTBI.
  8. Individuals who are unable to consent or who would usually be offered LTBI treatment under DOT because of their mental or social disabilities or those with drug or alcohol abuse
  9. Evidence of active TB

Sites / Locations

  • Shrewsbury Road Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention

Control

Arm Description

Participants with LTBI will be treated in the Community/Primary Care.

Participants with LTBI will be treated in the Hospital/TB Clinic

Outcomes

Primary Outcome Measures

Completion of Latent Tuberculosis Treatment
Based on patients taking at least 90 percent of doses of Rifinah during 3 months of treatment.

Secondary Outcome Measures

Complete of Latent Tuberculosis Treatment
Based on patients taking at least 80 or 85 percent of doses during 3 months of treatment.
Adherence to Treatment
To describe the proportion of individuals in the two treatment arms who adhere to LTBI treatment based on the five-point MARS5 (Medication Adherence Report Scale) questionairre, collection of prescriptions and a point of care urine testing for metabolites of isoniazid (Iso-screen) performed at monthly intervals.
Acceptability of Treatment
To describe the proportion of individuals in the two treatment arms who accept LTBI treatment. This is defined as those initiating treatment and attending TB clinics and community pharmacies on at least one occasion.
Adverse Effects of Treatment
To assess the incidence of adverse effects of treatment for LTBI, including adverse liver function tests or any other effects leading to cessation of treatment. This will be assessed using liver function test results, and a monthly questionnaire.
Active Tuberculosis
The incidence of active TB occurring within 2 years after enrolment. TB incidence in the intervention and control group will be compared and there will be a sub-analysis of examining those who did or did not accept or complete treatment. This will be performed through matching the study population with the national Enhanced TB Surveillance System, where information on all reported TB cases nationally are recorded.
Patient Satisfaction
Assessed using a standardised non-validated questionnaire (Likert scale)
Cost-effectiveness of Treatment
Assessed using a health economic model that includes locally and nationally agreed tariffs for latent tuberculosis treatment.
Patient Knowledge
The impact of patients knowledge about Latent Tuberculosis on treatment acceptance and completion will be assessed at baseline using a standardised non-validated questionnaire.

Full Information

First Posted
August 5, 2016
Last Updated
November 24, 2021
Sponsor
Queen Mary University of London
Collaborators
University College, London, Public Health England
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1. Study Identification

Unique Protocol Identification Number
NCT03069807
Brief Title
Completion and Acceptability of Treatment Across Primary Care and the commUnity for Latent Tuberculosis
Acronym
CATAPULT
Official Title
Can Latent Tuberculosis Infection (LTBI) in Recent Migrants be Treated Effectively and Safely in Primary Care? A Cluster Randomised Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
January 2017 (Actual)
Primary Completion Date
September 2019 (Actual)
Study Completion Date
March 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Queen Mary University of London
Collaborators
University College, London, Public Health England

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study investigates whether recent migrants to the United Kingdom are more likely to complete treatment for Latent Tuberculosis Infection (LTBI) if they are treated in the community (by General Practitioners/Family Doctors and pharmacists) than in a hospital TB clinic.
Detailed Description
People with dormant/latent TB (LTBI) have TB bacteria in their bodies, but do not have any symptoms because the bacteria are not active. The investigators know that recent migrants with LTBI from countries where TB is very common (incidence greater than 150 per 100 000) are at risk of developing active TB (their dormant bacteria become active) after they arrive in the UK. Active TB can be both infectious and deadly. The treatment for LTBI is three-month course of antibiotics. This significantly reduces the risk of developing active TB. This treatment is currently arranged and supervised by hospital clinics, however, many migrants do not attend and numbers of people completing antibiotics is low. This leaves many at risk of developing active TB. This study investigates whether a community (primary care) based approach to the treatment of LTBI, coordinated by general practices and local pharmacists, will achieve higher rates of antibiotic completion. The London Borough of Newham, in the UK, has amongst the highest rates of active TB in Western Europe. As part of a strategy to tackle this disease burden, an innovative model of care has been implemented in the borough in which GPs and pharmacists screen and treat migrants with LTBI. Our trial will evaluate whether primary care based management of LTBI leads to higher rates of treatment completion amongst recent migrants when compared to hospital based care. This approach would save money (both for the health service and for patients in terms of travels costs) and reduce numbers of new cases of active TB. The treatment for Latent Tuberculosis Infection will be 3 months of combined oral Rifampicin and Isoniazid with Pyridoxine. The dosage is weight dependent.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Latent Tuberculosis

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster-randomised trial evaluating treatment completion (the primary outcome), uptake, acceptability, safety and cost-effectiveness of treating latent tuberculosis infection (LTBI) in migrants in primary care, compared with secondary care.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
362 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Participants with LTBI will be treated in the Community/Primary Care.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Participants with LTBI will be treated in the Hospital/TB Clinic
Intervention Type
Other
Intervention Name(s)
Community/Primary Care
Intervention Description
The treatment of Latent Tuberculosis Infection (LTBI) in the community by General Practitioners (Family Doctors) and Pharmacists
Intervention Type
Other
Intervention Name(s)
Hospital/TB Clinic
Intervention Description
The treatment of Latent Tuberculosis Infection (LTBI) in the Hospital TB Clinic by specialist doctors and nurses
Primary Outcome Measure Information:
Title
Completion of Latent Tuberculosis Treatment
Description
Based on patients taking at least 90 percent of doses of Rifinah during 3 months of treatment.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Complete of Latent Tuberculosis Treatment
Description
Based on patients taking at least 80 or 85 percent of doses during 3 months of treatment.
Time Frame
3 months
Title
Adherence to Treatment
Description
To describe the proportion of individuals in the two treatment arms who adhere to LTBI treatment based on the five-point MARS5 (Medication Adherence Report Scale) questionairre, collection of prescriptions and a point of care urine testing for metabolites of isoniazid (Iso-screen) performed at monthly intervals.
Time Frame
3 months
Title
Acceptability of Treatment
Description
To describe the proportion of individuals in the two treatment arms who accept LTBI treatment. This is defined as those initiating treatment and attending TB clinics and community pharmacies on at least one occasion.
Time Frame
3 months
Title
Adverse Effects of Treatment
Description
To assess the incidence of adverse effects of treatment for LTBI, including adverse liver function tests or any other effects leading to cessation of treatment. This will be assessed using liver function test results, and a monthly questionnaire.
Time Frame
3 months
Title
Active Tuberculosis
Description
The incidence of active TB occurring within 2 years after enrolment. TB incidence in the intervention and control group will be compared and there will be a sub-analysis of examining those who did or did not accept or complete treatment. This will be performed through matching the study population with the national Enhanced TB Surveillance System, where information on all reported TB cases nationally are recorded.
Time Frame
2 years
Title
Patient Satisfaction
Description
Assessed using a standardised non-validated questionnaire (Likert scale)
Time Frame
3 months
Title
Cost-effectiveness of Treatment
Description
Assessed using a health economic model that includes locally and nationally agreed tariffs for latent tuberculosis treatment.
Time Frame
2 years
Title
Patient Knowledge
Description
The impact of patients knowledge about Latent Tuberculosis on treatment acceptance and completion will be assessed at baseline using a standardised non-validated questionnaire.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with LTBI aged 16-35 and who have entered the UK less than 5 years ago from a country with a TB incidence of greater than 150/100,000. Latent Tuberculosis is defined as a positive IGRA test without any symptoms or physical signs of active Tuberculosis and no evidence of active Tuberculosis on Chest X-ray. Exclusion Criteria: Pregnant or breastfeeding women Patients requiring medications that cannot be safely taken with Rifinah HIV infection. Individuals with known liver disease, or abnormal liver function tests (LFTs) Diagnosis of cirrhosis (jaundice, haematemesis, ascites or previous episodes of liver encephalopathy) Chronic or active hepatitis B or hepatitis C virus infection Previous treatment for TB or LTBI. Individuals who are unable to consent or who would usually be offered LTBI treatment under DOT because of their mental or social disabilities or those with drug or alcohol abuse Evidence of active TB
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heinke Kunst, MD MSc
Organizational Affiliation
Queen Mary University of London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shrewsbury Road Health Centre
City
London
ZIP/Postal Code
E7 8QP
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31783742
Citation
Burman M, Copas A, Zenner D, Hickson V, Gosce L, Trathen D, Ashcroft R, Martineau AR, Abubakar I, Griffiths C, Kunst H. Protocol for a cluster randomised control trial evaluating the efficacy and safety of treatment for latent tuberculosis infection in recent migrants within primary care: the CATAPuLT trial. BMC Public Health. 2019 Nov 29;19(1):1598. doi: 10.1186/s12889-019-7983-7.
Results Reference
derived

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Completion and Acceptability of Treatment Across Primary Care and the commUnity for Latent Tuberculosis

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