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Mobile Health Intervention for Active Tuberculosis

Primary Purpose

Tuberculosis, Adherence, Medication

Status
Completed
Phase
Not Applicable
Locations
Argentina
Study Type
Interventional
Intervention
Mobile phone TB treatment support app plus usual care
Usual care
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Tuberculosis focused on measuring mobile Health

Eligibility Criteria

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

Inclusion Criteria:

  • Subject is starting TB treatment for the first time
  • Subject has no known TB drug resistance
  • Subject is HIV negative (self-reported or documented)
  • Subject owns or has regular access to a mobile phone that can access the Internet and is able to operate the mobile phone to communicate or have someone able to assist.

Exclusion Criteria:

  • Severely ill (i.e., requiring hospitalization)
  • Reside in the same household with another study participant
  • History of known drug resistance and HIV co-infection because their care is managed separately and the treatment regimens and duration differ.

Sites / Locations

  • Hospital Dr. Antonio A. Cetrángolo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mobile phone TB treatment support app

Usual care

Arm Description

Daily use of the mobile phone TB treatment support app plus usual care. Participants will be asked to self-report daily TB medication administration, side-effects when applicable, and complete the direct adherence paper-based test randomly on 3-4 days of the week during the intensive treatment phase (first two months) and then 1-2 times per week during the maintenance phase (about month 3-6).

Usual care consists of outpatient treatment management from the time of diagnosis (unless symptoms are severe and hospitalization is recommended), routine clinical and laboratory tests, and follow-up appointments determined by the clinician. In general, patients receive 1-2 month's supply of medication and are asked to return monthly for follow-up.

Outcomes

Primary Outcome Measures

Acceptability (perceived usefulness and ease of use)
The Mobile Application Rating Scale (MARS) is a 19-item. The scale includes three sections and a modifiable app-specific section: classification, quality and satisfaction classification section provides descriptive information about the apps. The objective app quality section includes 19-items divided into four scales: engagement, functionality, aesthetics and information quality. The subjective quality section contains 4 items evaluating the user's overall satisfaction. MARS items are scored using a 5-point Likert scale. The final MARS scores include four subscale scores, a total mean score, subjective quality score and an app-specific subscale that assesses perceived impact on the user's knowledge, attitudes, and intentions to change as well as likelihood of changing targeted behaviors.
Feasibility of implementation
Semi-structured interview with participants to understand challenges, recommendations for improvement. Observations
Initial efficacy - Treatment outcome
Treatment outcomes will be measured using standard definitions set by the World Health Organization (WHO) Standards of TB treatment. Treatment success based on WHO definitions: completed (without bacteriological confirmation) or cured (negative sputum smear at 6 months and at least once prior to 6 months)). Other treatment outcomes include: failed (sputum smear positive at 5 months or later), died, defaulted (treatment interruption for ≥ 2 months), lost to follow-up (diagnosed, treatment outcome not documented), or transferred out (transferred to another reporting unit and treatment outcome is unknown).

Secondary Outcome Measures

Global Health Patient-Reported Outcomes Measurement Information System (PROMIS) short form
The Global Health short form (SF) is a recommended outcome measure for self-management, includes 10 items
Tuberculosis Knowledge Assessment Questionnaire
Items include questions focused on exploring knowledge about: causes and symptoms of TB (5 items), TB transmission (4 items), TB treatment (2 items), and TB prevention (5 items). The questions are structured to answer (yes, no, I don't know).
Engagement
Level of engagement using the app will be measured by percentage of notification without a reminder, number of questions, number of reported side effects.

Full Information

First Posted
May 21, 2018
Last Updated
December 8, 2020
Sponsor
University of Washington
Collaborators
National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT03544476
Brief Title
Mobile Health Intervention for Active Tuberculosis
Official Title
Interactive Mobile Health Intervention to Support Patients With Active Tuberculosis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
April 9, 2019 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
July 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Institute of Nursing Research (NINR)

4. Oversight

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

5. Study Description

Brief Summary
The purpose of this study is to evaluate and further refine a mobile support tool for patients receiving treatment for active tuberculosis. Half of participants will receive support and monitoring using a mobile phone software application and usual care, while the other half will receive usual care.
Detailed Description
Tuberculosis (TB) remains a top ten leading cause of death globally despite it being a largely curable disease. New effective treatment supervision strategies are needed particularly in low-resource high TB burden settings and a potential solution is in the hands of nearly every patient - a mobile phone. Modern modular design mobile phone software applications ("apps") hold great promise to address this unmet need. Current technologies allows for rapid design modification based on end user needs, implementation of native operating system (e.g., Android) versions for users with inconsistent internet access, and the integration of the patients' experiences with electronic health records using industry standards. Apps can perform multiple functions (e.g., automated reminders, symptom tracking, secure messaging, multi-media education). To date, few TB related apps have focused on patients as users, and none support patient engagement in self-management of their care or direct adherence monitoring. The research objectives are to understand end user needs and other stakeholder needs to build, refine, and pilot test an app to support patients self-administering treatment for active TB.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis, Adherence, Medication
Keywords
mobile Health

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mobile phone TB treatment support app
Arm Type
Experimental
Arm Description
Daily use of the mobile phone TB treatment support app plus usual care. Participants will be asked to self-report daily TB medication administration, side-effects when applicable, and complete the direct adherence paper-based test randomly on 3-4 days of the week during the intensive treatment phase (first two months) and then 1-2 times per week during the maintenance phase (about month 3-6).
Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
Usual care consists of outpatient treatment management from the time of diagnosis (unless symptoms are severe and hospitalization is recommended), routine clinical and laboratory tests, and follow-up appointments determined by the clinician. In general, patients receive 1-2 month's supply of medication and are asked to return monthly for follow-up.
Intervention Type
Behavioral
Intervention Name(s)
Mobile phone TB treatment support app plus usual care
Intervention Description
The behavioral intervention is delivered through a mobile phone TB support app. The functions allow the participant to: self-report daily administration of their TB medication, self-report side effects if applicable, review educational material on TB disease and its treatment, complete a treatment adherence monitoring test (urine drug metabolite test), take notes, and review their treatment progress/report. The drug metabolite test will require that the participant place a small amount of urine on the end of the paper strip, wait for results, and take a picture of the paper using the app. The purpose of this test is to confirm that medication was correctly taken within the past 24 hours.
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
Usual care consists of outpatient treatment management from the time of diagnosis (unless symptoms are severe and hospitalization is recommended), routine clinical and laboratory tests, and follow-up appointments determined by the clinician. In general, patients receive 1-2 month's supply of medication and are asked to return monthly for follow-up.
Primary Outcome Measure Information:
Title
Acceptability (perceived usefulness and ease of use)
Description
The Mobile Application Rating Scale (MARS) is a 19-item. The scale includes three sections and a modifiable app-specific section: classification, quality and satisfaction classification section provides descriptive information about the apps. The objective app quality section includes 19-items divided into four scales: engagement, functionality, aesthetics and information quality. The subjective quality section contains 4 items evaluating the user's overall satisfaction. MARS items are scored using a 5-point Likert scale. The final MARS scores include four subscale scores, a total mean score, subjective quality score and an app-specific subscale that assesses perceived impact on the user's knowledge, attitudes, and intentions to change as well as likelihood of changing targeted behaviors.
Time Frame
6 months
Title
Feasibility of implementation
Description
Semi-structured interview with participants to understand challenges, recommendations for improvement. Observations
Time Frame
6 months
Title
Initial efficacy - Treatment outcome
Description
Treatment outcomes will be measured using standard definitions set by the World Health Organization (WHO) Standards of TB treatment. Treatment success based on WHO definitions: completed (without bacteriological confirmation) or cured (negative sputum smear at 6 months and at least once prior to 6 months)). Other treatment outcomes include: failed (sputum smear positive at 5 months or later), died, defaulted (treatment interruption for ≥ 2 months), lost to follow-up (diagnosed, treatment outcome not documented), or transferred out (transferred to another reporting unit and treatment outcome is unknown).
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Global Health Patient-Reported Outcomes Measurement Information System (PROMIS) short form
Description
The Global Health short form (SF) is a recommended outcome measure for self-management, includes 10 items
Time Frame
day 1 and 6 months
Title
Tuberculosis Knowledge Assessment Questionnaire
Description
Items include questions focused on exploring knowledge about: causes and symptoms of TB (5 items), TB transmission (4 items), TB treatment (2 items), and TB prevention (5 items). The questions are structured to answer (yes, no, I don't know).
Time Frame
day 1 and 6 months
Title
Engagement
Description
Level of engagement using the app will be measured by percentage of notification without a reminder, number of questions, number of reported side effects.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject is starting TB treatment for the first time Subject has no known TB drug resistance Subject is HIV negative (self-reported or documented) Subject owns or has regular access to a mobile phone that can access the Internet and is able to operate the mobile phone to communicate or have someone able to assist. Exclusion Criteria: Severely ill (i.e., requiring hospitalization) Reside in the same household with another study participant History of known drug resistance and HIV co-infection because their care is managed separately and the treatment regimens and duration differ.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah Iribarren, PhD, RN
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Dr. Antonio A. Cetrángolo
City
Vicente López
State/Province
Province Of Buenos Aires
ZIP/Postal Code
1602
Country
Argentina

12. IPD Sharing Statement

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Mobile Health Intervention for Active Tuberculosis

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