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TB mHealth Study - Use of Cell Phones to Improve Compliance in Patients on LTBI Treatment

Primary Purpose

Latent Tuberculosis Infection

Status
Unknown status
Phase
Early Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Cell phone text messages
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Latent Tuberculosis Infection focused on measuring latent tuberculosis, text message interventions, medication adherence

Eligibility Criteria

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

Inclusion Criteria:

  1. Are initiating treatment for latent TB infection;
  2. Are over the age of 18 years old;
  3. Own a mobile phone or share access mobile phone access with a household member who consents to participate; AND
  4. Demonstrate sufficient ability to communicate via text messaging in English or have a family member or friend that is able to provide translation and assistance with text messaging for the duration of the study

Exclusion Criteria:

  1. Individuals under the age of 18;
  2. Unable to adequately send and receive text messages for any reason OR
  3. Enrolled in another clinical trial that may assess or influence treatment adherence.

Sites / Locations

  • New Westminster TB Control Clinic
  • Vancouver Downtown TB Control Clinic
  • Vancouver TB Control Clinic (VTC),

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Non-intervention

Cell phone intervention arm

Arm Description

Participants will only receive standard of care

Upon consent, participants will be randomly assigned to receive either 1) standard of care (9 months of INH or 4 months of RIF) and weekly SMS text messages via mobile phone or 2) standard of care (9 months of INH or months of RIF) without weekly SMS text messages via mobile phone.

Outcomes

Primary Outcome Measures

Successful completion of LTBI treatment regimens.
Successful treatment completion is defined as taking at least 80% of the doses of INH prescribed within 12 months or at least 80% of RIF prescribed within 6 months.

Secondary Outcome Measures

Full Information

First Posted
March 6, 2012
Last Updated
October 7, 2015
Sponsor
University of British Columbia
Collaborators
British Columbia Cancer Agency
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1. Study Identification

Unique Protocol Identification Number
NCT01549457
Brief Title
TB mHealth Study - Use of Cell Phones to Improve Compliance in Patients on LTBI Treatment
Official Title
The Effect of Weekly Text-message Communication on Treatment Completion Among Patients With Latent Tuberculosis Infection: a Randomised Controlled Trial (WelTel LTBI)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
April 2012 (undefined)
Primary Completion Date
October 2016 (Anticipated)
Study Completion Date
October 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia
Collaborators
British Columbia Cancer Agency

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will examine the impact of use of mobile phones and text messaging on adherence to treatment for patients with latent TB infection. Half (50%) of the 350 anticipated study participants will receive weekly text messages inquiring on their health status in relation to their prescribed treatment, while the other half (50%) will not receive weekly text messages at all. Medical adherence will be assessed by monthly blood-work, clinic visits and by interviewing patients at each of these visits. The investigators hypothesis is that enhanced communication with a health care provider, via a structured cell phone SMS text messaging based program (WelTel), will result in a 15% improvement in the proportion of patients who successfully complete their LTBI treatment regimens.
Detailed Description
Purpose The purpose of this study is to compare the proportion of patients who are adherent to their TB medications among those receiving weekly text messages plus standard of care and those who receive standard of care only. Justification: Previous research has shown that weekly text messages from a health care provider increases medication adherence for HIV patients. The investigators would like to determine if a similar effect in terms of adherence can be seen in patients receiving medication for latent tuberculosis infection Objectives Primary Objective: 1) To compare successful treatment completion rates for patients treated with 9 months of INH or 4 months of RIF between those receiving weekly SMS text messages via mobile phone plus standard of care to those receiving standard care. The standard of care at the TB clinics for all LTBI patients includes provision of a 30 day supply of medications - isoniazid 300mg daily for 9 months months or rifampin 600mg daily for 4 months - at a time, monthly blood-work and monthly clinic visits. Successful treatment completion is defined as taking at least 80% of the doses of INH prescribed within 12 months or at least 80% of the doses of RIF prescribed within 6 months. Secondary Objectives: To compare the proportion of prescribed doses taken on schedule (daily adherence) prior to medication discontinuation or interruption on medical advice between those receiving weekly SMS text messages via mobile phone to those receiving standard care; To measure patient satisfaction with the SMS intervention using a provider administered questionnaire including a series of Likert questions. 4) Research Method This study is a prospective open-label multicentre randomized controlled trial of a clinical intervention. It is estimated that 350 study participants will be required to have 80% power to detect a 15% difference in adherence at a .05 level of significance. In addition to recruiting English-speaking participants, the investigators will also be recruiting participants that have Chinese and Punjabi as their first language. Upon consent, participants will be randomly assigned to receive either 1) standard of care (9 months of INH or 4 months of RIF) and weekly SMS text messages via mobile phone or 2) standard of care (9 months of INH or 4 months of RIF) without weekly SMS text messages via mobile phone. The clinicians, pharmacists and researchers involved in evaluating compliance will not be blinded to the allocation of the intervention and control groups, as they will be required to review patients charts periodically, respond to patients text messages when they are experiencing difficulty in taking medications or side effects, as well as to ensure the successful operation of the SMS technology platform.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Latent Tuberculosis Infection
Keywords
latent tuberculosis, text message interventions, medication adherence

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Non-intervention
Arm Type
No Intervention
Arm Description
Participants will only receive standard of care
Arm Title
Cell phone intervention arm
Arm Type
Experimental
Arm Description
Upon consent, participants will be randomly assigned to receive either 1) standard of care (9 months of INH or 4 months of RIF) and weekly SMS text messages via mobile phone or 2) standard of care (9 months of INH or months of RIF) without weekly SMS text messages via mobile phone.
Intervention Type
Other
Intervention Name(s)
Cell phone text messages
Intervention Description
Participants in the intervention arm will receive weekly text messages from the TB control clinic asking how they are.
Primary Outcome Measure Information:
Title
Successful completion of LTBI treatment regimens.
Description
Successful treatment completion is defined as taking at least 80% of the doses of INH prescribed within 12 months or at least 80% of RIF prescribed within 6 months.
Time Frame
4 or 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Are initiating treatment for latent TB infection; Are over the age of 18 years old; Own a mobile phone or share access mobile phone access with a household member who consents to participate; AND Demonstrate sufficient ability to communicate via text messaging in English or have a family member or friend that is able to provide translation and assistance with text messaging for the duration of the study Exclusion Criteria: Individuals under the age of 18; Unable to adequately send and receive text messages for any reason OR Enrolled in another clinical trial that may assess or influence treatment adherence.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Richard Lester, MD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
New Westminster TB Control Clinic
City
New Westminster
State/Province
British Columbia
Country
Canada
Facility Name
Vancouver Downtown TB Control Clinic
City
Vancouver
State/Province
British Columbia
Country
Canada
Facility Name
Vancouver TB Control Clinic (VTC),
City
Vancouver
State/Province
British Columbia
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
34702229
Citation
El Joueidi S, Bardosh K, Musoke R, Tilahun B, Abo Moslim M, Gourlay K, MacMullin A, Cook VJ, Murray M, Mbaraga G, Nsanzimana S, Lester R. Evaluation of the implementation process of the mobile health platform 'WelTel' in six sites in East Africa and Canada using the modified consolidated framework for implementation research (mCFIR). BMC Med Inform Decis Mak. 2021 Oct 26;21(1):293. doi: 10.1186/s12911-021-01644-1.
Results Reference
derived
PubMed Identifier
29437940
Citation
Johnston JC, van der Kop ML, Smillie K, Ogilvie G, Marra F, Sadatsafavi M, Romanowski K, Budd MA, Hajek J, Cook V, Lester RT. The effect of text messaging on latent tuberculosis treatment adherence: a randomised controlled trial. Eur Respir J. 2018 Feb 7;51(2):1701488. doi: 10.1183/13993003.01488-2017. Print 2018 Feb.
Results Reference
derived
PubMed Identifier
24719431
Citation
van der Kop ML, Memetovic J, Patel A, Marra F, Sadatsafavi M, Hajek J, Smillie K, Thabane L, Taylor D, Johnston J, Lester RT. The effect of weekly text-message communication on treatment completion among patients with latent tuberculosis infection: study protocol for a randomised controlled trial (WelTel LTBI). BMJ Open. 2014 Apr 9;4(4):e004362. doi: 10.1136/bmjopen-2013-004362.
Results Reference
derived

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TB mHealth Study - Use of Cell Phones to Improve Compliance in Patients on LTBI Treatment

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