SMS-based Mobile Health Intervention for Nutritional Status and Treatment Outcome Among TB Patients
Primary Purpose
Tuberculosis, Undernutrition
Status
Unknown status
Phase
Not Applicable
Locations
Ethiopia
Study Type
Interventional
Intervention
SMS-based Mobile Health intervention
Sponsored by
About this trial
This is an interventional other trial for Tuberculosis focused on measuring Tuberculosis, Nutrition, Treatment outcome, SMS
Eligibility Criteria
Inclusion Criteria:
- Patient who is following their anti TB treatment for at most two weeks and below
- Patient who have their own mobile phone
- Patient who is able to read and understand national official language (Amharic)
Exclusion Criteria:
- Patient whose TB treatment regimen more than 6 months
- Patient who is pregnant and lactating mothers
- Patient who enrolled other Interventional research
Sites / Locations
- Addis Ababa Health Bureau
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
SMS group
Control group
Arm Description
Nutrition-related SMS messages in addition to standard of care TB treatment with directly observed therapy
Standard care of TB treatment with directly observed therapy alone
Outcomes
Primary Outcome Measures
Nutritional status change
The nutritional status of the patient will be assessed by Body Mass Index (BMI) that calculated through measuring the body weight and height of the patients using an electronic platform weight scale to the nearest 0.1 kg and height to the nearest centimeter using standardized meter.
Secondary Outcome Measures
Dietary practice change
Patient's dietary diversity practice will be assessed through a standardized tool adapted from FANTA Household Dietary Diversity Score
Treatment outcome
Treatment outcomes will be classified as per WHO Tuberculosis treatment guideline. The classification is made based on the smear sputum examination result at second, five and end of six months treatment and/or treatment completion status.
Full Information
NCT ID
NCT04242472
First Posted
January 20, 2020
Last Updated
January 23, 2020
Sponsor
Addis Ababa University
Collaborators
Fogarty International Center of the National Institute of Health
1. Study Identification
Unique Protocol Identification Number
NCT04242472
Brief Title
SMS-based Mobile Health Intervention for Nutritional Status and Treatment Outcome Among TB Patients
Official Title
SMS-based Mobile Health Intervention for Nutritional Status and Treatment Outcomes Among TB Patients in Addis Ababa, Ethiopia: A Cluster Randomized Trial (CRT)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 2020 (Anticipated)
Primary Completion Date
September 2020 (Anticipated)
Study Completion Date
March 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Addis Ababa University
Collaborators
Fogarty International Center of the National Institute of Health
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Ethiopia is one of the high burden Tuberculosis countries and Tuberculosis is still the leading cause of mortality due to communicable diseases in the country. Nutritional status is one of the predictors of TB treatment outcomes. Thus, the current practices need integration of nutritional intervention in the DOT using Mobile health intervention. However, to investigator's knowledge, there is no sufficient evidence on the effect SMS text Messaging Mobile Health intervention on nutritional status and TB treatment outcomes in Ethiopia.
Detailed Description
To ensure the quality of SMS intervention, nutritional related SMS text message will be developed systematically through reviewing literature, systematic reviews and guidelines and appropriate behavioral theories by involving experts and patients. Automated SMS will be sent from one computer database at the scheduled date and time. A validated questionnaire will be adapted and pre-tested to check for any error. Adequate sample size is calculated for both arms with the ratio of 1:1 allocation. Standardized Anthropometric measurement, FANTA Household Dietary Diversity Score and WHO TB treatment outcome classification will be used for assessing the outcome variables. The data collectors will be trained on the objective, screening of eligible participants, the procedure of data collection, and how to assure the quality and security of the data based on the protocol. Continuous supervision will be employed throughout the data collection and intervention period. The data will be collected electronically and will be exported to STATA for analysis. Intention to treat analysis and regression analysis model will be employed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis, Undernutrition
Keywords
Tuberculosis, Nutrition, Treatment outcome, SMS
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A Cluster Randomized Trial (CRT) with parallel design will be employed.
Masking
Outcomes Assessor
Masking Description
Participants and providers will not be blind to the study intervention. Nutrition and tuberculosis treatment outcomes will be assessed by two independent reviewers without knowledge of each participant's treatment allocation.
Allocation
Randomized
Enrollment
440 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
SMS group
Arm Type
Experimental
Arm Description
Nutrition-related SMS messages in addition to standard of care TB treatment with directly observed therapy
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Standard care of TB treatment with directly observed therapy alone
Intervention Type
Behavioral
Intervention Name(s)
SMS-based Mobile Health intervention
Intervention Description
Nutritional related SMS text message mobile health intervention will be provided to Tuberculosis patients.
Primary Outcome Measure Information:
Title
Nutritional status change
Description
The nutritional status of the patient will be assessed by Body Mass Index (BMI) that calculated through measuring the body weight and height of the patients using an electronic platform weight scale to the nearest 0.1 kg and height to the nearest centimeter using standardized meter.
Time Frame
Change from baseline BMI at end of 2 months and 6 months treatment
Secondary Outcome Measure Information:
Title
Dietary practice change
Description
Patient's dietary diversity practice will be assessed through a standardized tool adapted from FANTA Household Dietary Diversity Score
Time Frame
Change from baseline dietary practice at end of 6 months treatment
Title
Treatment outcome
Description
Treatment outcomes will be classified as per WHO Tuberculosis treatment guideline. The classification is made based on the smear sputum examination result at second, five and end of six months treatment and/or treatment completion status.
Time Frame
End of six months TB treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient who is following their anti TB treatment for at most two weeks and below
Patient who have their own mobile phone
Patient who is able to read and understand national official language (Amharic)
Exclusion Criteria:
Patient whose TB treatment regimen more than 6 months
Patient who is pregnant and lactating mothers
Patient who enrolled other Interventional research
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zekariyas Sa Nezenega
Phone
911072963
Ext
+251
Email
zekitiru@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Damen Haile Mariam
Phone
929438641
Ext
+251
Email
damengoog@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Damen Haile Mariam
Organizational Affiliation
Addis Ababa University School of Public Health
Official's Role
Study Chair
Facility Information:
Facility Name
Addis Ababa Health Bureau
City
Addis Ababa
Country
Ethiopia
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yohannes Dr
Phone
911384599
Ext
+251
Email
yoha2wok@yahoo.com
First Name & Middle Initial & Last Name & Degree
Zekariyas Sa Nezenega, MPH
First Name & Middle Initial & Last Name & Degree
Damen Haile Mariam, PhD
First Name & Middle Initial & Last Name & Degree
Jeffrey collins, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
SMS-based Mobile Health Intervention for Nutritional Status and Treatment Outcome Among TB Patients
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