Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
301 participants
INTERVENTIONAL
2014-10-31
2016-12-31
Brief Summary
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Detailed Description
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Because of the high risk of both TB and HIV among the household contacts of TB patients and the importance of early case detection for both diseases and especially for DR-TB, improving TB case finding is a high priority. Recent studies have shown that having healthcare workers make multiple visits to the homes of TB patients in order to screen household contacts is a logistically challenging and resource- intensive strategy, and it is not routinely undertaken in most public sector settings in South Africa. One alternative to home visits that could prove effective and affordable is to offer small economic rewards to the household contacts of TB patients who voluntarily present at a healthcare facility for TB symptom screening and optional HIV testing. Economic incentives have been successful in increasing demand for healthcare in a variety of settings, but they have not been tried before as a way to increase uptake of services among patients' contacts, rather than among the diagnosed patients themselves.
This pilot project is an evaluation of the feasibility and results of offering an economic reward, in the form of a shopping voucher, to the household contacts of index patients (outpatient drug-susceptible and drug-resistant TB patients) who present at the study clinic for TB screening and optional HIV testing, providing a reward to the index patients for participating, and entering index patients whose contacts do present into a lottery to win a prize. The effectiveness of the intervention in screening a high proportion of contacts will be compared to existing published data from studies of active case-finding through home visits and of the status quo passive case finding. If successful, this pilot project will create a demand for screening among high risk patients, who will be rewarded for identifying themselves to the healthcare system, and could prove to be an affordable alternative to resource-intensive home visits. It will also shift responsibility for contact tracing from overburdened clinic staff to those who have the most to gain from early case detection-the patients and their families.
Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Contacts
Contacts are the household contacts of confirmed TB and drug-resistant TB patients.
Contacts
Household contacts who come to the study clinic, present a referral card, and complete TB symptom screening will receive a shopping voucher of $5-10 value.
Index
Index subjects are confirmed TB and drug-resistant TB patients who distribute referral cards to their household contacts.
Index
Index subjects will be entered in a prize lottery if any of their contacts complete TB symptom screening at the study clinic.
Interventions
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Contacts
Household contacts who come to the study clinic, present a referral card, and complete TB symptom screening will receive a shopping voucher of $5-10 value.
Index
Index subjects will be entered in a prize lottery if any of their contacts complete TB symptom screening at the study clinic.
Eligibility Criteria
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Inclusion Criteria
* Newly diagnosed with pulmonary TB (drug-susceptible or drug-resistant) or initiating treatment for TB at one of the study sites
* Usually spend at least 4 nights per week in the same household as an index case
* Can provide referral card given to contact by index patient
* Experience with the intervention as provider or patient
* Written informed consent to be interviewed
Exclusion Criteria
* No household contacts (live alone)
* Admitted for inpatient care immediately following their TB diagnosis, and thus not readily able to distribute the referral cards
* Not physically, mentally, or emotionally able to participate in the study, in the view of study staff
* Previously enrolled in the same study
* Declines to provide written informed consent to participate
* Unable to speak any of the languages for which consent documents are available and not accompanied by person who can
* Currently on any type of TB treatment
* Not able to present any form of identification that matches the information on the referral card
* Previously enrolled in the same study
* Declines to provide written informed consent to participate
* Unable to speak any of the languages for which consent documents are available and not accompanied by person who can
• None
ALL
No
Sponsors
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University of Witwatersrand, South Africa
OTHER
City of Johannesburg
UNKNOWN
Helen Joseph Hospital
OTHER
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Boston University
OTHER
Responsible Party
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Principal Investigators
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Sydney Rosen
Role: PRINCIPAL_INVESTIGATOR
Boston University
Locations
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Helen Joseph Hospital
Johannesburg, , South Africa
OR Tambo Clinic
Johannesburg, , South Africa
Countries
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Other Identifiers
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M140529
Identifier Type: OTHER
Identifier Source: secondary_id
H-33047
Identifier Type: -
Identifier Source: org_study_id
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