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Package of Care to Improve Retention in ART and Mortality Among Treatment Naive HIV Infected Individuals (PRAN)

Primary Purpose

HIV

Status
Completed
Phase
Phase 4
Locations
Nepal
Study Type
Interventional
Intervention
Package of HIV care
Standard HIV care
Sponsored by
National Centre for AIDs and STD Control, Nepal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV focused on measuring Package of care, Rapid Initiation of antiretroviral therapy, Advanced HIV disease, mHealth, Acquired Immunodeficiency Syndrome, Management of advance HIV disease

Eligibility Criteria

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

Inclusion Criteria:

  • Age greater than or equal to 16 years
  • Diagnosed with HIV-infection
  • ART-naive
  • Consent for study participation

Exclusion Criteria:

  • Age less than or equal to 15 years
  • Any previous use of ART

Sites / Locations

  • Sukraraj Tropical & Infectious Disease Control Hospital
  • Bharatpur District Hospital
  • Rapti Sub Regional Hospital
  • Seti Zonal Hospital
  • Tikapur Hospital
  • Mahakali Zonal Hospital
  • National Academy of Medical Science (NAMS), Bir Hospital
  • Tribhuvan University Teaching Hospital
  • Western Regional Hospital
  • B.P. Koirala Institute of Health Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Package of HIV care

Standard HIV care

Arm Description

Screening and management (Preventive / Pre-emptive therapies dosages) of different opportunistic infections (OI), Rapid antiretroviral therapy (ART) initiation and Enhanced adherence support.

Screening and management of common OIs, basic health assessment (CD4, viral load and other tests), ARV drugs and follow up.

Outcomes

Primary Outcome Measures

Mortality
All-cause mortality over the first 24 weeks after starting ART

Secondary Outcome Measures

Retention in treatment
PLHIV alive and on ART over the first 48 weeks after starting ART
Adherence to ART
Adherence will be assessed on a monthly basis (total pills taken by patient in last month/ total pills prescribed to patient in last month).
Morbidity
Incidence of opportunistic infection and immune reconstitution inflammatory syndrome (IRIS)
Viral load suppression
PLHIV and on ART who have a suppressed viral load (<1000 copies/mL)
Cost effectiveness of Package of care
Intervention cost will be calculated from estimates of the per-patient quantity of services used in delivery of package of care. Cost per death prevented and cost per DALY gained.
Mortality
All-cause mortality over the first 96 weeks after starting ART
Hospitalization
Hospital inpatient episodes and total days admitted

Full Information

First Posted
October 11, 2018
Last Updated
September 18, 2020
Sponsor
National Centre for AIDs and STD Control, Nepal
Collaborators
Sukraraj Tropical and Infectious Disease Hospital, National Academy of Medical Sciences, Nepal, Tribhuvan University Teaching Hospital, Institute Of Medicine., Rapti Sub-regional Hospital, Western Regional Hospital, Seti Zonal Hospital, Tikapur Hospital, Mahakali Zonal Hospital, Bharatpur Eye Hospital, B.P. Koirala Institute of Health Sciences, Expertise France, Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT03723525
Brief Title
Package of Care to Improve Retention in ART and Mortality Among Treatment Naive HIV Infected Individuals
Acronym
PRAN
Official Title
Evaluation of World Health Organization (WHO) Recommendations on Test and Treat Strategy, Managing Advanced HIV Disease and Rapid Initiation of ART Among People Living With HIV in Nepal: A Cluster Randomized Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
January 22, 2018 (Actual)
Primary Completion Date
December 24, 2019 (Actual)
Study Completion Date
December 24, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Centre for AIDs and STD Control, Nepal
Collaborators
Sukraraj Tropical and Infectious Disease Hospital, National Academy of Medical Sciences, Nepal, Tribhuvan University Teaching Hospital, Institute Of Medicine., Rapti Sub-regional Hospital, Western Regional Hospital, Seti Zonal Hospital, Tikapur Hospital, Mahakali Zonal Hospital, Bharatpur Eye Hospital, B.P. Koirala Institute of Health Sciences, Expertise France, Karolinska Institutet

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
This is a cluster randomized trial to determine whether a package of care including rapid antiretroviral therapy (ART) initiation, as compared to standard ART initiation, improves mortality, retention in care and viral suppression among treatment naive people living with HIV (PLHIV) in Nepal. Package of care includes immediate screening and treatment of opportunistic infections (OIs), rapid ART initiation and enhanced retention in care using mobile health (mHealth) and weekly/biweekly home-based adherence/ retention support linked to community care centre. Standard of care includes screening and management of common OIs, baseline assessment (CD4, viral load and other tests), antiretroviral drugs and ART follow up.
Detailed Description
PRAN is an open-label trial of 1000 Treatment-Naive PLHIV aged 16 years or more. To evaluate whether a package of care including rapid ART initiation [diagnosis and management of opportunistic infection (OI), rapid ART initiation and enhanced adherence support] is more effective in reducing morbidity and mortality, as compared to standard ART initiation, among ART naïve PLHIV in Nepal. To evaluate whether a package of care including rapid ART initiation is more effective in improving retention in HIV treatment, as compared to standard ART initiation, among ART naïve PLHIV in Nepal. To evaluate whether a package of care including rapid ART initiation improves viral suppression among ART naïve PLHIV in Nepal to a higher extent than standard ART initiation, To evaluate whether the different components of care act synergistically to improve mortality, retention in care and viral suppression among treatment Naive PLHIV, as compared to standard ART initiation, To assess the cost-effectiveness of this package of care intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV
Keywords
Package of care, Rapid Initiation of antiretroviral therapy, Advanced HIV disease, mHealth, Acquired Immunodeficiency Syndrome, Management of advance HIV disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1073 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Package of HIV care
Arm Type
Experimental
Arm Description
Screening and management (Preventive / Pre-emptive therapies dosages) of different opportunistic infections (OI), Rapid antiretroviral therapy (ART) initiation and Enhanced adherence support.
Arm Title
Standard HIV care
Arm Type
Experimental
Arm Description
Screening and management of common OIs, basic health assessment (CD4, viral load and other tests), ARV drugs and follow up.
Intervention Type
Combination Product
Intervention Name(s)
Package of HIV care
Other Intervention Name(s)
Screening and management of opportunistic infection, Rapid ART initiation and Enhanced adherence support
Intervention Description
A. Screening and management (Preventive / Pre-emptive therapies dosages) of different opportunistic infections (OI). Detail information mentioned in the manual (refer to uploaded protocol). B. Rapid ART Initiation PLHIV without suspicion or active OI: Initiate ART within seven days or same day after HIV serology disclosure PLHIV with suspicion or active OI: Defer initiation if clinical symptoms suggest tuberculosis or cryptococcal meningitis. Detail information mentioned in the manual (refer to uploaded protocol). C. Enhanced Adherence/Retention Support: mHealth: Receive text messages in mobile regarding appointment reminder (pill pick up, CD4 test, viral load test, early infant diagnosis (EID) test etc.) and general awareness messages (positive prevention, the importance of regular health check-up etc.). PLHIV with advanced HIV disease will also receive weekly/biweekly home-based adherence/ retention support linked to community care centre and community home-based care.
Intervention Type
Combination Product
Intervention Name(s)
Standard HIV care
Intervention Description
Standard of HIV care includes screening and management of OI (OI- tuberculosis (TB), bacterial pneumonia, herpes, and candidiasis), baseline assessment (CD4 and other blood tests- complete blood count, hemoglobin, platelets, liver function test, renal function test, urine for albumin, chest x-ray), at 6 months CD4 test, viral load (twice a year) and then on a yearly basis, additional lab test at 3 months, 6 months, antiretroviral (ARV) toxicity monitoring like hemoglobin (Zidovudine), Serum Glutamic-Pyruvic Transaminase (Nevirapine/Efavirenz), Creatinine (Tenofovir), prophylaxis (Co-trimoxazole preventive therapy CD4<350 and WHO stage III and IV and Isoniazid preventive therapy if eligible) and ART / follow up (generally monthly/ bimonthly).
Primary Outcome Measure Information:
Title
Mortality
Description
All-cause mortality over the first 24 weeks after starting ART
Time Frame
Week 24
Secondary Outcome Measure Information:
Title
Retention in treatment
Description
PLHIV alive and on ART over the first 48 weeks after starting ART
Time Frame
Week 48
Title
Adherence to ART
Description
Adherence will be assessed on a monthly basis (total pills taken by patient in last month/ total pills prescribed to patient in last month).
Time Frame
Week 0-48
Title
Morbidity
Description
Incidence of opportunistic infection and immune reconstitution inflammatory syndrome (IRIS)
Time Frame
Week 48
Title
Viral load suppression
Description
PLHIV and on ART who have a suppressed viral load (<1000 copies/mL)
Time Frame
Week 48
Title
Cost effectiveness of Package of care
Description
Intervention cost will be calculated from estimates of the per-patient quantity of services used in delivery of package of care. Cost per death prevented and cost per DALY gained.
Time Frame
Week 48
Title
Mortality
Description
All-cause mortality over the first 96 weeks after starting ART
Time Frame
Week 48
Title
Hospitalization
Description
Hospital inpatient episodes and total days admitted
Time Frame
0-48
Other Pre-specified Outcome Measures:
Title
Cryptococcal antigen
Description
Burden of serum cryptococcal antigen positive in PLHIV with CD4 < 100/mL
Time Frame
Week 48
Title
Immune Reconstitution Inflammatory Syndrome (IRIS)
Description
Burden of IRIS
Time Frame
Week 48
Title
CD4 cell count
Description
Changes in CD4 cell count
Time Frame
Week 48

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age greater than or equal to 16 years Diagnosed with HIV-infection ART-naive Consent for study participation Exclusion Criteria: Age less than or equal to 15 years Any previous use of ART
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Basu Dev Pandey, MD, PhD
Organizational Affiliation
National Centre for AIDS and STD Control
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bir B Rawal, MA
Organizational Affiliation
National Centre for AIDS and STD Control
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rajan K Bhattarai, MPH
Organizational Affiliation
Save the Children
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rajya Shree Nyachhyon Kunwar, MBBS, MPH
Organizational Affiliation
National Centre for AIDS and STD Control/ Global Fund Programs
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Upendra Shrestha, MPH
Organizational Affiliation
National Centre for AIDS and STD Control/ Global Fund Programs
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rajesh Khanal, MSc
Organizational Affiliation
National Centre for AIDS and STD Control/ Global Fund Programs
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marie Lagrange-Xelot, MD
Organizational Affiliation
Expertise France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tristan Delory, MD
Organizational Affiliation
Expertise France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anna Mia Ekstrom, MD, MPH, PhD
Organizational Affiliation
Dept of Infectious Diseases Karolinska University Hospital & Dept of Public Health (Global Health/IHCAR), Karolinska Institutet, Stockholm
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tara Nath Pokharel, MD, MPH
Organizational Affiliation
National Centre for AIDS and STD Control
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Keshab Deuba, MMSc, PhD
Organizational Affiliation
National Centre for AIDS and STD Control/ Global Fund Programs
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sukraraj Tropical & Infectious Disease Control Hospital
City
Kathmandu
State/Province
Bagmati
Country
Nepal
Facility Name
Bharatpur District Hospital
City
Bharatpur
Country
Nepal
Facility Name
Rapti Sub Regional Hospital
City
Dang
Country
Nepal
Facility Name
Seti Zonal Hospital
City
Kailālī
Country
Nepal
Facility Name
Tikapur Hospital
City
Kailālī
Country
Nepal
Facility Name
Mahakali Zonal Hospital
City
Kanchanpur
Country
Nepal
Facility Name
National Academy of Medical Science (NAMS), Bir Hospital
City
Kathmandu
Country
Nepal
Facility Name
Tribhuvan University Teaching Hospital
City
Kathmandu
Country
Nepal
Facility Name
Western Regional Hospital
City
Pokhara
Country
Nepal
Facility Name
B.P. Koirala Institute of Health Sciences
City
Sunsari
Country
Nepal

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29341560
Citation
Guidelines for Managing Advanced HIV Disease and Rapid Initiation of Antiretroviral Therapy. Geneva: World Health Organization; 2017. No abstract available. Available from http://www.ncbi.nlm.nih.gov/books/NBK475977/
Results Reference
background
PubMed Identifier
26192873
Citation
INSIGHT START Study Group; Lundgren JD, Babiker AG, Gordin F, Emery S, Grund B, Sharma S, Avihingsanon A, Cooper DA, Fatkenheuer G, Llibre JM, Molina JM, Munderi P, Schechter M, Wood R, Klingman KL, Collins S, Lane HC, Phillips AN, Neaton JD. Initiation of Antiretroviral Therapy in Early Asymptomatic HIV Infection. N Engl J Med. 2015 Aug 27;373(9):795-807. doi: 10.1056/NEJMoa1506816. Epub 2015 Jul 20.
Results Reference
background
PubMed Identifier
29352723
Citation
Molina JM, Grund B, Gordin F, Williams I, Schechter M, Losso M, Law M, Ekong E, Mwelase N, Skoutelis A, Wiselka MJ, Vandekerckhove L, Benfield T, Munroe D, Lundgren JD, Neaton JD; INSIGHT START study group. Which HIV-infected adults with high CD4 T-cell counts benefit most from immediate initiation of antiretroviral therapy? A post-hoc subgroup analysis of the START trial. Lancet HIV. 2018 Apr;5(4):e172-e180. doi: 10.1016/S2352-3018(18)30003-1. Epub 2018 Jan 16.
Results Reference
background

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Package of Care to Improve Retention in ART and Mortality Among Treatment Naive HIV Infected Individuals

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