Nutritional Support for HIV-Tuberculosis Co-infected Adults in Senegal, West Africa
Primary Purpose
HIV and Tuberculosis Co-infection
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Food basket
Ready-to-Use Therapeutic Food
Sponsored by
About this trial
This is an interventional health services research trial for HIV and Tuberculosis Co-infection
Eligibility Criteria
Inclusion Criteria:
- HIV-Tuberculosis co-infection
- Age ≥18 years
- Initiating treatment for tuberculosis
- Provide written informed consent
Exclusion Criteria:
• Unwilling or unable to provide written informed consent
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Food basket
Ready-to-Use Therapeutic Food
Arm Description
Outcomes
Primary Outcome Measures
Uptake, as determined by percent of monthly nutritional support rations received, transported, stored, and utilized by subjects.
Acceptability, as determined by patient reported perceptions of nutritional support.
Costs of monthly nutritional support rations.
Secondary Outcome Measures
Tuberculosis treatment adherence as determined by Medication Possession Ratio
Tuberculosis treatment adherence as determined by patient reported number of missed doses in the previous 7 days and 4 weeks.
Tuberculosis treatment completion defined as completing full course of prescribed therapy
Adherence to antiretroviral therapy as determined by Medication Possession Ratio
Adherence to antiretroviral therapy as determined by patient reported number of missed doses in the previous 7 days and 4 weeks
CD4 cell count
Presence of acid fast bacteria using sputum smear microscopy
Results of GeneXpert
Nutritional status as determined by Body Mass Index
Nutritional status as determined by change in weight (kg)
Food security status measured using the Household Food Insecurity Access Scale (HFIAS)
The HFIAS is a 9-item questionnaire which provides a household food insecurity score on a scale of 1-4, with 1 being not food insecure, 2 being mildly food insecure, 3 being moderately food insecure, and 4 being severely food insecure.
Hemoglobin levels (g/dl)
Full Information
NCT ID
NCT03711721
First Posted
October 8, 2018
Last Updated
October 17, 2018
Sponsor
University of Washington
Collaborators
La Clinique des Maladies Infectieuses, Centre Hospitalier National Universitaire de Fann
1. Study Identification
Unique Protocol Identification Number
NCT03711721
Brief Title
Nutritional Support for HIV-Tuberculosis Co-infected Adults in Senegal, West Africa
Official Title
Nutritional Support to Improve Adherence and Treatment Completion Among HIV-Tuberculosis Co-infected Adults in Senegal, West Africa: A Randomized Pilot Implementation Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
June 2016 (Actual)
Primary Completion Date
August 2017 (Actual)
Study Completion Date
August 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
La Clinique des Maladies Infectieuses, Centre Hospitalier National Universitaire de Fann
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
Food insecurity can contribute to poor adherence to both tuberculosis treatment and antiretroviral therapy (ART). Interventions that target food insecurity have the potential to improve treatment adherence and decrease mortality. The goals of this study were to determine the cost, feasibility, acceptability, and potential impact of implementing nutritional support to improve adherence and treatment completion among HIV-TB co-infected adults in the Casamance region of Senegal, West Africa.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV and Tuberculosis Co-infection
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Food basket
Arm Type
Experimental
Arm Title
Ready-to-Use Therapeutic Food
Arm Type
Experimental
Intervention Type
Dietary Supplement
Intervention Name(s)
Food basket
Intervention Type
Dietary Supplement
Intervention Name(s)
Ready-to-Use Therapeutic Food
Primary Outcome Measure Information:
Title
Uptake, as determined by percent of monthly nutritional support rations received, transported, stored, and utilized by subjects.
Time Frame
6 months
Title
Acceptability, as determined by patient reported perceptions of nutritional support.
Time Frame
6 months
Title
Costs of monthly nutritional support rations.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Tuberculosis treatment adherence as determined by Medication Possession Ratio
Time Frame
6 months
Title
Tuberculosis treatment adherence as determined by patient reported number of missed doses in the previous 7 days and 4 weeks.
Time Frame
6 months
Title
Tuberculosis treatment completion defined as completing full course of prescribed therapy
Time Frame
6 months
Title
Adherence to antiretroviral therapy as determined by Medication Possession Ratio
Time Frame
6 months
Title
Adherence to antiretroviral therapy as determined by patient reported number of missed doses in the previous 7 days and 4 weeks
Time Frame
6 months
Title
CD4 cell count
Time Frame
6 months
Title
Presence of acid fast bacteria using sputum smear microscopy
Time Frame
6 months
Title
Results of GeneXpert
Time Frame
6 months
Title
Nutritional status as determined by Body Mass Index
Time Frame
6 months
Title
Nutritional status as determined by change in weight (kg)
Time Frame
6 months
Title
Food security status measured using the Household Food Insecurity Access Scale (HFIAS)
Description
The HFIAS is a 9-item questionnaire which provides a household food insecurity score on a scale of 1-4, with 1 being not food insecure, 2 being mildly food insecure, 3 being moderately food insecure, and 4 being severely food insecure.
Time Frame
6 months
Title
Hemoglobin levels (g/dl)
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
HIV-Tuberculosis co-infection
Age ≥18 years
Initiating treatment for tuberculosis
Provide written informed consent
Exclusion Criteria:
• Unwilling or unable to provide written informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Noelle A Benzekri, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Moussa Seydi, MD
Organizational Affiliation
La Clinique des Maladies Infectieuses, CHNU de Fann
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
31318879
Citation
Benzekri NA, Sambou JF, Tamba IT, Diatta JP, Sall I, Cisse O, Thiam M, Bassene G, Badji NM, Faye K, Sall F, Malomar JJ, Seydi M, Gottlieb GS. Nutrition support for HIV-TB co-infected adults in Senegal, West Africa: A randomized pilot implementation study. PLoS One. 2019 Jul 18;14(7):e0219118. doi: 10.1371/journal.pone.0219118. eCollection 2019.
Results Reference
derived
Learn more about this trial
Nutritional Support for HIV-Tuberculosis Co-infected Adults in Senegal, West Africa
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