Latent Tuberculosis Clinical Trial
— TXT4MEDOfficial title:
Promoting Adherence to Treatment for Latent TB Infection Through Mobile Phone Text Messaging
NCT number | NCT02690818 |
Other study ID # | TXT4MED |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2016 |
Est. completion date | September 26, 2018 |
Verified date | April 2019 |
Source | University of Arizona |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this pilot study is to determine whether regularly scheduled medication reminder text messages (SMS) are effective in increasing latent tuberculosis infection (LTBI) treatment completion.
Status | Completed |
Enrollment | 30 |
Est. completion date | September 26, 2018 |
Est. primary completion date | September 26, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Consent to the study - Own a mobile phone which operates on a telecom provider supported by our SMS platform - Initiating or actively receiving treatment for LTBI at the Pima County TB Clinic in Tucson, AZ - Prescribed self-administered therapy - Report not having prior or current active TB disease - Know how to and are able to receive SMS messages - At least 18 years of age Exclusion Criteria: - Do not meet inclusion criteria - Do not consent to study |
Country | Name | City | State |
---|---|---|---|
United States | Pima County Health Department | Tucson | Arizona |
Lead Sponsor | Collaborator |
---|---|
University of Arizona | American Lung Association, Pima County Health Department |
United States,
Oren E, Bell ML, Garcia F, Perez-Velez C, Gerald LB. Promoting adherence to treatment for latent TB infection through mobile phone text messaging: study protocol for a pilot randomized controlled trial. Pilot Feasibility Stud. 2017 Mar 13;3:15. doi: 10.1186/s40814-017-0128-9. eCollection 2017. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Recruitment | How many approached by clinic, how many referred, how many study eligible, how many consented; why ineligible or refused; how long to recruit each patient | Ongoing | |
Secondary | Retention | How many drop out at each monthly time point, who and why | Ongoing | |
Secondary | Perceptions of Intervention through a questionnaire | Perceptions and opinions (if the intervention was helpful, non-helpful, effectiveness) in the intervention arm will be assessed after the study follow-up through a questionnaire of a subset of enrolled individuals at the completion of the participant's treatment (up to 12 months post-treatment initiation). | Once, up to 12 months post-treatment |
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