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"Conducting A Study On Video Observed Therapy In The Management Of Tuberculosis" (VOT)

Primary Purpose

Tuberculosis

Status
Not yet recruiting
Phase
Not Applicable
Locations
Malaysia
Study Type
Interventional
Intervention
VIDEO OBSERVED THERAPY
Sponsored by
University of Malaya
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Tuberculosis focused on measuring Tuberculosis, Digital health, video observed therapy, treatment adherence

Eligibility Criteria

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

Inclusion Criteria: i. All PTB smear-positive patients. ii. Patients aged 18 years and above. iii. Possess a digital phone or other equivalent gadget equipped with a WhatsApp application. iv. Able to accurately identify each TB medication. Exclusion Criteria: i. Recurrent PTB infection. ii. Patients who are extremely ill, have no proper social support, no caretakers, and are hospitalized. iii. Patients in prison during the time of diagnosis or treatment.

Sites / Locations

  • Hospital Sultanah Nur Zahira

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

CONTROL

INTERVENTION ARM (VOT)

Arm Description

The control group, traditional DOTS is the group who will be attending daily to their respective PR-1/PR-2 throughout intensive phase.

The intervention group, video observed therapy (VOT) is the group who will be teleconferencing daily with their respective PR-1/PR-2 TB team via WhatsApp throughout the intensive phase.

Outcomes

Primary Outcome Measures

Treatment adherence in percentage from both arms
Number of days medicine consumed/over 60 days intensive period

Secondary Outcome Measures

Seroconversion rate
Number of successful sero-conversion patients from sputum smear positive to sputum smear negative by the end of the intensive phase.
Side effects incidents report
Number of reported side effects detected from both arms.
Patients suffering with side effects
Number of patients having side effects detected from both arms.
Degree of patient's satisfaction
The degree of satisfaction of the participants from both arms.
Time save
Overall time spent by patients from both arms.
Cost saving
Overall money spent by patients from both arms.

Full Information

First Posted
July 19, 2023
Last Updated
August 15, 2023
Sponsor
University of Malaya
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1. Study Identification

Unique Protocol Identification Number
NCT05994144
Brief Title
"Conducting A Study On Video Observed Therapy In The Management Of Tuberculosis"
Acronym
VOT
Official Title
"Effectiveness of Video Observed Therapy in the Management of Tuberculosis"
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 1, 2023 (Anticipated)
Primary Completion Date
March 30, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Malaya

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 aim of this study is to measure the effectiveness usage of VOT in the treatment of TB in terms of treatment adherence. The study will be a randomized controlled trial and will involve 240 TB patients. The study is aimed to commence by December 2023. The study period will be for 4 months.
Detailed Description
There is an urgent need to produce an integrated e-health system in tackling the issue of remote monitoring for patient adherence. For example, in TB infection which requires close monitoring for better treatment outcomes. The usage of digital health products replacing the traditional DOTS will be a cost-effective method and will also bode convenient for patients and staff. Video Observed Therapy (VOT) usage as the alternative digital health method replacing traditional DOTS will be more effective in tackling adherence issues. This method has already been tried in many countries like the United States of America (USA), the United Kingdom (UK), Italy, and Moldova, and has proven to be more effective than traditional DOTS. For instance, a study by Story et al. reveals that a total of 70% of patients on VOT successfully completed ≥80% of a 2-month observation compared with only 31% of those on traditional DOTS (95% CI 3.10 to 9.68). A proposed intervention of adapting VOT in TB treatment is a practical move, as it can improve treatment compliance and also has the added benefit of being cost-effective. 1.4 Research Question What is the effectiveness of Video Observed Therapy (VOT) in the management of tuberculosis (TB) compared to the traditional Directly Observed Treatment Short Course Strategy (DOTS)? 1.5 Study Objectives 1.5.1 General Objective The general objective of this study is to compare the effectiveness of VOT with traditional DOTS in the management of TB. 1.5.2 Specific Objectives I. To develop VOT intervention in the management of TB. II. To compare the effectiveness of VOT as compared to traditional DOTS. III. To measure patient satisfaction using VOT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
Tuberculosis, Digital health, video observed therapy, treatment adherence

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
For all participants who are randomised into VOT arm or traditional DOTS arm. Control group : Patients allocated into the traditional DOTS arm will follow the usual protocol as all other patients assigned to DOTS under Ministry of Health Malaysia Intervention group : Patient will be observed on their daily TB medication consumption via teleconference by using WhatsApp video call.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CONTROL
Arm Type
No Intervention
Arm Description
The control group, traditional DOTS is the group who will be attending daily to their respective PR-1/PR-2 throughout intensive phase.
Arm Title
INTERVENTION ARM (VOT)
Arm Type
Active Comparator
Arm Description
The intervention group, video observed therapy (VOT) is the group who will be teleconferencing daily with their respective PR-1/PR-2 TB team via WhatsApp throughout the intensive phase.
Intervention Type
Other
Intervention Name(s)
VIDEO OBSERVED THERAPY
Intervention Description
Video-observed therapy is the usage of teleconferencing to observe anti-TB medication ingestion.
Primary Outcome Measure Information:
Title
Treatment adherence in percentage from both arms
Description
Number of days medicine consumed/over 60 days intensive period
Time Frame
60 days
Secondary Outcome Measure Information:
Title
Seroconversion rate
Description
Number of successful sero-conversion patients from sputum smear positive to sputum smear negative by the end of the intensive phase.
Time Frame
60 days
Title
Side effects incidents report
Description
Number of reported side effects detected from both arms.
Time Frame
60 days
Title
Patients suffering with side effects
Description
Number of patients having side effects detected from both arms.
Time Frame
60 days
Title
Degree of patient's satisfaction
Description
The degree of satisfaction of the participants from both arms.
Time Frame
Questionnaire using Likert scale. "Score 1:least satisfied,Score 5: most satisfied"
Title
Time save
Description
Overall time spent by patients from both arms.
Time Frame
120 days
Title
Cost saving
Description
Overall money spent by patients from both arms.
Time Frame
60 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: i. All PTB smear-positive patients. ii. Patients aged 18 years and above. iii. Possess a digital phone or other equivalent gadget equipped with a WhatsApp application. iv. Able to accurately identify each TB medication. Exclusion Criteria: i. Recurrent PTB infection. ii. Patients who are extremely ill, have no proper social support, no caretakers, and are hospitalized. iii. Patients in prison during the time of diagnosis or treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
KARTIK KALIYANA SUNDARAM, MPH
Phone
0060124975343
Email
kartik25@hotmail.com
Facility Information:
Facility Name
Hospital Sultanah Nur Zahira
City
Kuala Terengganu
State/Province
Terengganu
Country
Malaysia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD WILL NOT BE SHARED FOR UNSPECIFIED REASONS

Learn more about this trial

"Conducting A Study On Video Observed Therapy In The Management Of Tuberculosis"

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