TB Treatment Support Tool Interactive Mobile App and Direct Adherence Monitoring on TB Treatment Outcomes (TB-TST)
Primary Purpose
Tuberculosis, Treatment Adherence
Status
Active
Phase
Not Applicable
Locations
Argentina
Study Type
Interventional
Intervention
TB treatment assistant
Sponsored by
About this trial
This is an interventional treatment trial for Tuberculosis focused on measuring treatment supervision, success default
Eligibility Criteria
Inclusion Criteria:
- Participants must be at least 16 years old,
- have a new diagnosis of drug-susceptible TB,
- First treatment
- have regular access to a smartphone, and
- be able to operate the phone or have someone able to assist.
Exclusion Criteria:
- Children up to 15 years old
- Retreatment (default or previous treatment failure)
- Patients who are severely ill (i.e., requiring hospitalization)
- Patients who reside in the same household with another study participant
- Inability to operate a smartphone
- Illiteracy (inability to read and write)
- Patients with known drug resistance
- Patients with known HIV co-infection will be excluded because their care is managed separately.
- Screened patients who do not meet study eligibility will have specific screening data (including gender, age and reason for exclusion) entered into the study database to examine reasons for exclusion and feasibility of enrollment criteria.
Case definition: Patients at least 16 year old with TB confirmed by smear-positive sputum or diagnosis of pulmonary TB based on radiological findings and clinical signs and symptoms but with negative sputum smear. The diagnosis may be confirmed by other methods, such as, MGIT960, BACTEC 9000 or MB Bact, nucleic acid amplification (PCR) or ELISA.
Sites / Locations
- IECS
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
intervention: TB treatment assistant
Control
Arm Description
Patients receiving instructions to use phone application
Patients receiving instructions for usual care self administered treatment
Outcomes
Primary Outcome Measures
Treatment success
Completion of treatment and or cure
Treatment default
Abandonment of treatment for at least 2 months
Secondary Outcome Measures
Full Information
NCT ID
NCT04221789
First Posted
January 6, 2020
Last Updated
April 28, 2023
Sponsor
Institute for Clinical Effectiveness and Health Policy
Collaborators
University of Washington
1. Study Identification
Unique Protocol Identification Number
NCT04221789
Brief Title
TB Treatment Support Tool Interactive Mobile App and Direct Adherence Monitoring on TB Treatment Outcomes
Acronym
TB-TST
Official Title
TB Treatment Support Tools: Refinement and Evaluation of an Interactive Mobile App and Direct Adherence Monitoring on TB Treatment Outcomes
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 17, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
June 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute for Clinical Effectiveness and Health Policy
Collaborators
University of Washington
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The overall goal of this study is to conduct a Randomized Clinical Trial (RCT) to evaluate a tuberculosis treatment support tool (TB-TST), a cellular phone app developed using user-centered design principles and a paper-based drug metabolite urine test strip modified for home use for testing the presence of isoniazid drug metabolites in urine to directly monitor adherence to treatment, to improve treatment outcomes for patients with TB receiving self-administered treatment (SAT).
Poor medication adherence to TB regimens, along with challenges in monitoring patients and returning them to treatment, are important contributing factors to poor outcomes and the development of drug resistance. With advances and proliferation of mobile technology platforms, there is substantial interest in the possible use of mobile health (mHealth) interventions to address these challenges. Of the mHealth approaches under investigation for TB adherence monitoring, drug metabolite testing has been identified as the most promising, ethical, and accurate, and the least intrusive and stigmatizing strategy compared to other mobile solutions, yet its potential remains largely unexplored. Additionally, mobile applications (apps) may provide personalized treatment supervision, increase patients' self-management and improve patient-provider communication by offering more advanced functionalities for patient support and monitoring.
The existing version of the TB-TST app offers education on TB and its treatment, communication with a care-coordinator, tracks treatment adherence (both by self-reporting and direct metabolite test strip images), self-reports treatment side-effects, and retains patient's "diary" notes. This proposal builds on preliminary work to: 1) Refine the TB-TST intervention based on pilot study findings and apply principles of user-centered design; 2) Evaluate the impact of the TB-TST on treatment outcomes compared to usual care; 3) Assess patient and provider perceptions of the facilitators and barriers to implementation of the TB-TST and synthesize lessons learned with stakeholders and policy makers. Primary outcome will be treatment success. Secondary outcomes will include: treatment default rates, self-reported adherence, technology use and usability. Findings have broader implications not only for TB adherence but disease management more generally and will improve our understanding of how to support patients facing challenging treatment regimens
Detailed Description
Tuberculosis remains one of the top ten causes of death globally despite it being largely curable. Patients face many challenges to adhere to treatment and mobile health (mHealth) interventions may address these challenges and support patients to complete their treatment. We will improve an interactive intervention based on the combined input from patients and TB experts and evaluate the intervention's impact on treatment outcomes in a randomized clinical trial. Findings have broader implications not only for TB adherence but disease management more generally and will improve our understanding of how to support patients in challenging treatment regimens.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis, Treatment Adherence
Keywords
treatment supervision, success default
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Data analysts will not be aware of group allocation
Allocation
Randomized
Enrollment
555 (Actual)
8. Arms, Groups, and Interventions
Arm Title
intervention: TB treatment assistant
Arm Type
Experimental
Arm Description
Patients receiving instructions to use phone application
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients receiving instructions for usual care self administered treatment
Intervention Type
Other
Intervention Name(s)
TB treatment assistant
Other Intervention Name(s)
TB-TST (Treatment Support Tools)
Intervention Description
Cell phone app to support self administered treatment and monitor adherence
Primary Outcome Measure Information:
Title
Treatment success
Description
Completion of treatment and or cure
Time Frame
6 months
Title
Treatment default
Description
Abandonment of treatment for at least 2 months
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Participants must be at least 16 years old,
have a new diagnosis of drug-susceptible TB,
First treatment
have regular access to a smartphone, and
be able to operate the phone or have someone able to assist.
Exclusion Criteria:
Children up to 15 years old
Retreatment (default or previous treatment failure)
Patients who are severely ill (i.e., requiring hospitalization)
Patients who reside in the same household with another study participant
Inability to operate a smartphone
Illiteracy (inability to read and write)
Patients with known drug resistance
Patients with known HIV co-infection will be excluded because their care is managed separately.
Screened patients who do not meet study eligibility will have specific screening data (including gender, age and reason for exclusion) entered into the study database to examine reasons for exclusion and feasibility of enrollment criteria.
Case definition: Patients at least 16 year old with TB confirmed by smear-positive sputum or diagnosis of pulmonary TB based on radiological findings and clinical signs and symptoms but with negative sputum smear. The diagnosis may be confirmed by other methods, such as, MGIT960, BACTEC 9000 or MB Bact, nucleic acid amplification (PCR) or ELISA.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fernando A Rubinstein, MD MPH
Organizational Affiliation
Institute for Clinical Effectiveness and Health Policy
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sarah Iribarren, RN PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
IECS
City
Buenos Aires
ZIP/Postal Code
1414
Country
Argentina
12. IPD Sharing Statement
Plan to Share IPD
No
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TB Treatment Support Tool Interactive Mobile App and Direct Adherence Monitoring on TB Treatment Outcomes
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