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Evaluating the Effectiveness of Interactive SMS Reminders on TB Treatment Outcomes

I

Interactive Research and Development

Status

Completed

Conditions

Tuberculosis

Treatments

Other: Interactive Reminders

Study type

Interventional

Funder types

Other

Identifiers

NCT01690754
IRD_IRB_2011_03_002

Details and patient eligibility

About

In this study, Interactive Research and Development (IRD) in Karachi, Pakistan is evaluating the impact of Interactive Reminders on drug compliance and treatment outcomes. Interactive Reminders is an interactive SMS reminder system to help patients remember to take their TB medication. In this system, patients receive daily SMS reminders for the duration of their treatment at a pre-specified time, reminding them to take their medication. Patients are asked to reply back to the system, either through SMS or a missed call, with the time they took their medicine that day. If a response is not received within two hours, a second reminder is sent. If a response is still not received in a further two hours, a third and final reminder for the day is sent. Non-responsive patients are followed up with phone calls and a list of non-responsive patients is shared with clinics based on the parameters of non-responsiveness that they specify.

IRD seeks to determine the impact of this system on treatment outcomes and compliance to prescribed medication through administering a randomized control trial among newly diagnosed TB patients in Karachi, Pakistan.

Enrollment

2,207 patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • New, smear-positive drug susceptible TB who have been on treatment for less than two weeks
  • Access to a mobile phone (self-reported)
  • Intending to reside in Karachi for the duration of their treatment

Exclusion criteria

  • Patients who do not have regular access to a mobile phone
  • Patients who have previously received TB treatment
  • Patients who have another member in their household who is already a part of the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

2,207 participants in 2 patient groups

Control
No Intervention group
Description:
This arm will receive the regular standard of care given by TB clinics.
Interactive Reminders
Experimental group
Description:
Patients randomized to this arm will receive Interactive SMS reminders daily.
Treatment:
Other: Interactive Reminders

Trial contacts and locations

11

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Data sourced from clinicaltrials.gov

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