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Clinical Trials/ISRCTN95243114
ISRCTN95243114
Completed
未知

Intervening with a Manualised Package to achieve treatment adherence in people with Tuberculosis: the IMPACT study

Joint Research Office0 sites79 target enrollmentFebruary 14, 2018
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ConditionsTuberculosis, improving adherence to treatment.Infections and InfestationsTuberculosis

Overview

Phase
未知
Intervention
Not specified
Conditions
Tuberculosis, improving adherence to treatment.
Sponsor
Joint Research Office
Enrollment
79
Status
Completed
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2019 Protocol article in https://pubmed.ncbi.nlm.nih.gov/31852704/ protocol (added 12/11/2020) 2021 Interim results article in https://pubmed.ncbi.nlm.nih.gov/33898764/ Qualitative study (added 14/11/2022) 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34049611/ Scoping review (added 14/11/2022) 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34584407/ Scoping review (added 14/11/2022)

Registry
who.int
Start Date
February 14, 2018
End Date
May 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Joint Research Office

Eligibility Criteria

Inclusion Criteria

  • •1\. Individuals aged over 18 being started on treatment for TB affecting any site.
  • •2\. Migrants newly arrived in the UK
  • •3\. People whose first language is not English
  • •4\. Woman who are pregnant
  • •5\. People with a mental health disorder
  • •6\. People taking immunosuppressive therapy or known to have immunodeficiency
  • •7\. Those with a previous history of treatment for TB or non\-adherence with anti\-TB medication
  • •8\. People with a current or previous history of drug or alcohol misuse

Exclusion Criteria

  • •1\. Patients already on treatment for TB at the point they attend the TB services in the study
  • •2\. If the patient is not expected to live for the duration of treatment (that is a minimum of six months from starting treatment)
  • •3\. Age under 16

Outcomes

Primary Outcomes

Not specified

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