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Link4Health: A Combination Strategy for Linkage and Retention, Swaziland (L4H)

Primary Purpose

HIV (Human Immunodeficiency Virus)

Status
Completed
Phase
Not Applicable
Locations
Swaziland
Study Type
Interventional
Intervention
POC (point-of-care) CD4+ (cluster of differentiation 4) Count
Accelerated ART (antiretroviral therapy) Initiation
Basic Care and Prevention Package
Cellular Appointment Reminders and Follow-Up
Financial Incentive
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV (Human Immunodeficiency Virus) focused on measuring HIV (Human Immunodeficiency Virus), ART (antiretroviral therapy), financial incentive, linkage, retention, SMS (Short Message Service) appointment reminder, accelerated ART, CD4+ count

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years
  • Testing HIV-positive at an HTC (HIV testing and counseling) site within a SU (study unit)
  • Willing to be referred to an HIV care clinic associated with the SU
  • Willing to provide locator information
  • Willing to adhere to study procedures, including a baseline interview, home-based interviews at 1 and 12 months after study enrollment; home-based CD4+ count assessment 12 months after enrollment, and abstraction of data from their medical records.
  • Able to provide informed consent

Exclusion Criteria:

  • Planning on leaving the community where they currently reside in the next 12 months for a period greater than 6 months
  • Enrolled in HIV (Human immunodeficiency virus) care in the past 6 months at any HIV care clinic
  • Currently on ART (antiretroviral therapy)
  • Initiated ART (for any duration) in the past 6 months at any HIV care clinic
  • Does not speak or understand English or si-Swati
  • Reports being currently pregnant at time of study enrollment

Sites / Locations

  • Bhalekane Clinic
  • Dvokolwako
  • Good Shepherd Hospital
  • Hlatikhulu Hospital
  • Horo
  • Kamfishane
  • Lamvelase
  • Luyengo Clinic
  • Mangweni Clinic
  • Mankayane Hospital
  • Mashobneni Clinic
  • Mbabane Government Hospital
  • Mkhuzweni Health Center
  • Motshane
  • Mpolenjeni Clinic
  • Nhlangano Health Center
  • Piggs Peak
  • Raleigh Fitkin Memorial Hospital
  • Siphofaneni Clinc
  • Sithobeloa Rural Health Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard of Care

Combined Intervention Strategy

Arm Description

Participants will be managed per standard of care following prevailing Swaziland Ministry of Health guidelines.

Point-of-care (POC) CD4+ (cluster of differentiation 4) Count Accelerated ART initiation for ART eligible participants Basic care and prevention package Cellular Appointment Reminders and Follow-Up Financial Incentives

Outcomes

Primary Outcome Measures

Change in proportion of participants who both link to care at assigned study unit within 1 month and are retained in care at the designated study unit 12 months after HIV (Human Immunodeficiency Virus) diagnosis
Combined outcome of linkage to HIV care within 1 month after testing HIV positive and retention in care 12 months after testing. Participants are considered to achieve this outcome if they successfully link to the HIV clinic at their study unit (SU) within 1 month of testing HIV positive and are retained in care at the HIV clinic at their SU 12 months after testing HIV positive, as measured from medical records.

Secondary Outcome Measures

Proportion of participants successfully linked to care at designated study unit within 1 month of HIV diagnosis
Linkage to care within 1 month of HIV testing (at any clinic within the assigned study unit).
Proportion of participants retained in care at designated study unit 12 months after HIV diagnosis.
Retention in care 12 months after HIV testing, independent of linkage at 1 month (at any clinic within the assigned study unit).
Change in proportion of participants successfully linked to care at any HIV care clinic within one month of HIV diagnosis
Proportion of participants successfully linked to care at any HIV care clinic within one month of HIV diagnosis
Median time from HIV testing to initial assessment of ART (antiretroviral) eligibility
Time from linkage to ART eligibility assessment
Median time from HIV testing to ART eligibility
Time from HIV testing to ART eligibility
Proportion of participants who consistently engage in care (attend > 75% of scheduled appointments)
Proportion of participants who consistently engage in care, defined as attend > 75% of scheduled appointments
Change in proportion of participants with new World Health Organization (WHO) Stage III/IV event or hospitalization
Proportion of participants with new WHO Stage III/IV event or hospitalization
Median CD4+ (cluster difference 4) count and viral load 12 months after HIV diagnosis
Median CD4+ cell count 12 months after HIV diagnosis, median viral load 12 months after HIV diagnosis
Change in Mortality rate
Mortality rate 12 months after HIV diagnosis
Change in proportion of participants reporting interventions were received
Proportion of participants, who are randomized to study units receiving CIS, reporting receipt of each intervention
Proportion of participants reporting that interventions were highly acceptable
Proportion of participants, who are randomized to study units receiving CIS, reporting that interventions were highly acceptable

Full Information

First Posted
July 16, 2013
Last Updated
October 20, 2021
Sponsor
Columbia University
Collaborators
National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases (NIAID), Centers for Disease Control and Prevention, New York University
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1. Study Identification

Unique Protocol Identification Number
NCT01904994
Brief Title
Link4Health: A Combination Strategy for Linkage and Retention, Swaziland
Acronym
L4H
Official Title
LINK4HEALTH: A Combination Approach to Linkage and Retention for HIV (Human Immunodeficiency Virus) Infected Individuals in Swaziland
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
August 2013 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
October 12, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Columbia University
Collaborators
National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases (NIAID), Centers for Disease Control and Prevention, New York University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Despite increased HIV (Human Immunodeficiency Virus) infection testing in Africa, many patients never enroll in subsequent HIV care after testing or remain in care after an initial enrollment. This study's aim is to improve linkage to HIV care and retention in HIV care through the use of feasible, evidence-based, and practical interventions. The study takes place in Swaziland, the country with the highest HIV prevalence (24%) in sub-Saharan Africa. The study will randomize groups of HIV testing sites and affiliated clinics to either standard of care or a combined intervention strategy (CIS) which consists of point-of care CD4 (cluster differentiation 4 (CD4)) testing at time of HIV testing, fast-track HIV medications for those who are eligible for treatment,mobile phone appointment reminders, care bags filled with health prevention materials, and financial incentives. The study outcomes are linkage to and retention in care as well as cost effectiveness, feasibility of interventions, and patient acceptability of interventions.
Detailed Description
Linkage of patients from HIV testing to HIV care programs and their retention once enrolled in care are essential to HIV program effectiveness in terms of prevention of HIV;related morbidity and mortality and prevention of HIV transmission. Linkage and retention rates in HIV programs in sub-Saharan Africa (SSA) are suboptimal, with less than half of patients who test positive successfully linking and remaining in care at 1 year. This study is a two-arm cluster site;randomized trial to compare the effectiveness of a novel combination package of evidence;based interventions, the combination intervention strategy (CIS), compared to standard of care (SOC) on linkage and retention of HIV;positive patients from point of testing to retention in care. CIS will include 1) point of care CD4+ count assays at HIV testing sites; 2) accelerated antiretroviral therapy (ART) initiation for eligible patients; 3) provision of a basic care and prevention package (BCPP); 4) short message service (SMS) reminders for clinic appointments; and 5) financial incentives for linkage and retention. The primary aim is to evaluate the effectiveness of CIS as compared to SOC on the combined outcome of rapid linkage to HIV care within 1 month and retention in care at 12 months among adults testing positive for HIV. Secondary aims include evaluation of the effectiveness of CIS compared to SOC on each of linkage to HIV; retention in care; time to ART initiation; HIV disease progression and mortality; patient acceptability; association between baseline characteristics and outcomes, and comparison of cost effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV (Human Immunodeficiency Virus)
Keywords
HIV (Human Immunodeficiency Virus), ART (antiretroviral therapy), financial incentive, linkage, retention, SMS (Short Message Service) appointment reminder, accelerated ART, CD4+ count

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2201 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Participants will be managed per standard of care following prevailing Swaziland Ministry of Health guidelines.
Arm Title
Combined Intervention Strategy
Arm Type
Experimental
Arm Description
Point-of-care (POC) CD4+ (cluster of differentiation 4) Count Accelerated ART initiation for ART eligible participants Basic care and prevention package Cellular Appointment Reminders and Follow-Up Financial Incentives
Intervention Type
Procedure
Intervention Name(s)
POC (point-of-care) CD4+ (cluster of differentiation 4) Count
Other Intervention Name(s)
PIMA
Intervention Description
Each HIV testing and counseling (HTC) site will be equipped with POC CD4+ testing using PIMA™ Analyser (Inverness), test strips, and reagents. Study staff will obtain 25 microliters of blood via finger prick and process the POC (point-of-care) CD4+ (cluster of differentiation 4) Count' test immediately following the baseline interview. Test results will be recorded on study forms including a referral form that has multiple copies, one copy to be given to the participant, the second sent to the affiliated HIV (Human immunodeficiency virus)care clinic in the study unit, and the third kept by study staff in a locked cabinet with other confidential material. All participants, regardless of the CD4+ result, will be encouraged to enroll in HIV care as soon as they can.
Intervention Type
Procedure
Intervention Name(s)
Accelerated ART (antiretroviral therapy) Initiation
Intervention Description
Accelerated ART initiation for patients with POC CD4+ < 350 cells/uL (micro-liter) within 1 week from testing. 2 counseling sessions (one at time of HTC and other at first HIV clinic visit), and collection of blood for other baseline lab tests, but initiation prior to return of results for patients who do not meet criteria for waiting
Intervention Type
Behavioral
Intervention Name(s)
Basic Care and Prevention Package
Other Intervention Name(s)
BCPP
Intervention Description
Basic care and prevention package (BCPP) provided approximately every three months that includes: condoms; soap, pill box and pictorial education about use of materials and HIV, such as family testing tools and information. Information on BCPP contents and review the educational materials will be provided. An example of educational materials is a family-testing tool to encourage the participant to have all family members tested for HIV. All BCPP items will be replenished every 3 months for all participants, regardless of ART status, beginning at linkage to HIV care.
Intervention Type
Behavioral
Intervention Name(s)
Cellular Appointment Reminders and Follow-Up
Intervention Description
SMS (short messaging service) appointment reminders for follow-up appointments. Telephone call within 7 days of missed appointment for all patients.
Intervention Type
Other
Intervention Name(s)
Financial Incentive
Other Intervention Name(s)
FI (Financial Incentive)
Intervention Description
Participants will receive a series of financial incentives to support linkage into care within 1 month and retention in care at 6 months and 12 months after testing HIV positive. The value of the financial incentive (FI) will be 80 Swaziland Rand, calculated based on the associated financial costs of traveling to clinic. These incentives will be distributed by through mobile airtime. Participants without mobile phones will be given an alternative incentive of equal value, such as a store voucher.
Primary Outcome Measure Information:
Title
Change in proportion of participants who both link to care at assigned study unit within 1 month and are retained in care at the designated study unit 12 months after HIV (Human Immunodeficiency Virus) diagnosis
Description
Combined outcome of linkage to HIV care within 1 month after testing HIV positive and retention in care 12 months after testing. Participants are considered to achieve this outcome if they successfully link to the HIV clinic at their study unit (SU) within 1 month of testing HIV positive and are retained in care at the HIV clinic at their SU 12 months after testing HIV positive, as measured from medical records.
Time Frame
one month after enrollment, 12 months after enrollment
Secondary Outcome Measure Information:
Title
Proportion of participants successfully linked to care at designated study unit within 1 month of HIV diagnosis
Description
Linkage to care within 1 month of HIV testing (at any clinic within the assigned study unit).
Time Frame
12 months after enrollment
Title
Proportion of participants retained in care at designated study unit 12 months after HIV diagnosis.
Description
Retention in care 12 months after HIV testing, independent of linkage at 1 month (at any clinic within the assigned study unit).
Time Frame
12 months after enrollment
Title
Change in proportion of participants successfully linked to care at any HIV care clinic within one month of HIV diagnosis
Description
Proportion of participants successfully linked to care at any HIV care clinic within one month of HIV diagnosis
Time Frame
one month after enrollment, 12 months after enrollment
Title
Median time from HIV testing to initial assessment of ART (antiretroviral) eligibility
Description
Time from linkage to ART eligibility assessment
Time Frame
12-months after enrollment
Title
Median time from HIV testing to ART eligibility
Description
Time from HIV testing to ART eligibility
Time Frame
12 months after enrollment
Title
Proportion of participants who consistently engage in care (attend > 75% of scheduled appointments)
Description
Proportion of participants who consistently engage in care, defined as attend > 75% of scheduled appointments
Time Frame
12-months after enrollment
Title
Change in proportion of participants with new World Health Organization (WHO) Stage III/IV event or hospitalization
Description
Proportion of participants with new WHO Stage III/IV event or hospitalization
Time Frame
1 month after enrollment,12 months after enrollment
Title
Median CD4+ (cluster difference 4) count and viral load 12 months after HIV diagnosis
Description
Median CD4+ cell count 12 months after HIV diagnosis, median viral load 12 months after HIV diagnosis
Time Frame
12 months after testing HIV-positive
Title
Change in Mortality rate
Description
Mortality rate 12 months after HIV diagnosis
Time Frame
1 month after enrollment, 12 months after enrollment
Title
Change in proportion of participants reporting interventions were received
Description
Proportion of participants, who are randomized to study units receiving CIS, reporting receipt of each intervention
Time Frame
1 month after enrollment, 12 months after enrollment
Title
Proportion of participants reporting that interventions were highly acceptable
Description
Proportion of participants, who are randomized to study units receiving CIS, reporting that interventions were highly acceptable
Time Frame
12 months after enrollment
Other Pre-specified Outcome Measures:
Title
Change in adjusted risk ratio comparing proportion of participants who both link to care at assigned study unit within one month and are retained in care at designated study unit twelve months after HIV diagnosis
Description
Adjusted risk ratio comparing proportion of participants who both link to care at assigned study unit within one month and are retained in care at designated study unit twelve months after HIV diagnosis, by strata of age, sex, and other socio-demographic variables
Time Frame
at enrollment, one month after enrollment, 12 months after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years Testing HIV-positive at an HTC (HIV testing and counseling) site within a SU (study unit) Willing to be referred to an HIV care clinic associated with the SU Willing to provide locator information Willing to adhere to study procedures, including a baseline interview, home-based interviews at 1 and 12 months after study enrollment; home-based CD4+ count assessment 12 months after enrollment, and abstraction of data from their medical records. Able to provide informed consent Exclusion Criteria: Planning on leaving the community where they currently reside in the next 12 months for a period greater than 6 months Enrolled in HIV (Human immunodeficiency virus) care in the past 6 months at any HIV care clinic Currently on ART (antiretroviral therapy) Initiated ART (for any duration) in the past 6 months at any HIV care clinic Does not speak or understand English or si-Swati Reports being currently pregnant at time of study enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wafaa El-Sadr, MD MPH
Organizational Affiliation
ICAP Columbia University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Charles Azih, MD MPH
Organizational Affiliation
Swaziland MOH
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Scott Braithwaite, MD MSc
Organizational Affiliation
New York University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Batya Elul, PhD MD
Organizational Affiliation
ICAP Columbia University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Peter Ehrenkranz, MD MPH
Organizational Affiliation
Centers for Disease Control and Prevention
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Matthew Lamb, PhD MPH
Organizational Affiliation
ICAP Columbia University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Margaret McNairy, MD MSc
Organizational Affiliation
ICAP Columbia University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Phumzile Mndzebele
Organizational Affiliation
Swaziland MOH
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ruben Sahabao, MD
Organizational Affiliation
ICAP Swaziland
Official's Role
Study Director
Facility Information:
Facility Name
Bhalekane Clinic
City
Swaziland
Country
Swaziland
Facility Name
Dvokolwako
City
Swaziland
Country
Swaziland
Facility Name
Good Shepherd Hospital
City
Swaziland
Country
Swaziland
Facility Name
Hlatikhulu Hospital
City
Swaziland
Country
Swaziland
Facility Name
Horo
City
Swaziland
Country
Swaziland
Facility Name
Kamfishane
City
Swaziland
Country
Swaziland
Facility Name
Lamvelase
City
Swaziland
Country
Swaziland
Facility Name
Luyengo Clinic
City
Swaziland
Country
Swaziland
Facility Name
Mangweni Clinic
City
Swaziland
Country
Swaziland
Facility Name
Mankayane Hospital
City
Swaziland
Country
Swaziland
Facility Name
Mashobneni Clinic
City
Swaziland
Country
Swaziland
Facility Name
Mbabane Government Hospital
City
Swaziland
Country
Swaziland
Facility Name
Mkhuzweni Health Center
City
Swaziland
Country
Swaziland
Facility Name
Motshane
City
Swaziland
Country
Swaziland
Facility Name
Mpolenjeni Clinic
City
Swaziland
Country
Swaziland
Facility Name
Nhlangano Health Center
City
Swaziland
Country
Swaziland
Facility Name
Piggs Peak
City
Swaziland
Country
Swaziland
Facility Name
Raleigh Fitkin Memorial Hospital
City
Swaziland
Country
Swaziland
Facility Name
Siphofaneni Clinc
City
Swaziland
Country
Swaziland
Facility Name
Sithobeloa Rural Health Center
City
Swaziland
Country
Swaziland

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29112963
Citation
McNairy ML, Lamb MR, Gachuhi AB, Nuwagaba-Biribonwoha H, Burke S, Mazibuko S, Okello V, Ehrenkranz P, Sahabo R, El-Sadr WM. Effectiveness of a combination strategy for linkage and retention in adult HIV care in Swaziland: The Link4Health cluster randomized trial. PLoS Med. 2017 Nov 7;14(11):e1002420. doi: 10.1371/journal.pmed.1002420. eCollection 2017 Nov.
Results Reference
derived
PubMed Identifier
26189154
Citation
McNairy ML, Gachuhi AB, Lamb MR, Nuwagaba-Biribonwoha H, Burke S, Ehrenkranz P, Mazibuko S, Sahabo R, Philip NM, Okello V, El-Sadr WM. The Link4Health study to evaluate the effectiveness of a combination intervention strategy for linkage to and retention in HIV care in Swaziland: protocol for a cluster randomized trial. Implement Sci. 2015 Jul 19;10:101. doi: 10.1186/s13012-015-0291-4.
Results Reference
derived

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Link4Health: A Combination Strategy for Linkage and Retention, Swaziland

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