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Integrating Hypertension and Cardiovascular Diseases Care Into Existing HIV Services Package in Botswana (InterCARE) (InterCARE)

Primary Purpose

HIV Infections, Hypertension

Status
Recruiting
Phase
Not Applicable
Locations
Botswana
Study Type
Interventional
Intervention
InterCARE package
Sponsored by
University of Botswana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for HIV Infections

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria for participants:

  • Adults aged 20-75 years old
  • Documented HIV-infection on ART
  • Confirmed diagnosis of hypertension or elevated blood pressure >140/90mmHg versus >130/80mmHg if they have underlying Diabetes Mellitus or Chronic Kidney Disease
  • Receiving regular care at the selected clinics

Exclusion Criteria:

● Positive for HIV-related dementia

Inclusion criteria for participants' treatment partners:

  • Adults aged 18 years of age or older
  • Selected to be a treatment partner by participant.

Sites / Locations

  • Phitsane-Molopo IDCC ClinicRecruiting
  • Tonota IDCC Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

InterCARE package

Arm Description

Outcomes

Primary Outcome Measures

Primary quantitative implementation outcome 1a
Change from baseline in % of patients with HIV who are aware of their hypertension
Primary quantitative implementation outcome 1b
Change from baseline in % of patients with HIV who are aware of their hypertension
Primary quantitative implementation outcome 2a
Effectiveness - The proportion with controlled blood pressure as measured by blood pressure readings taken at the 6 months study visit
Primary quantitative implementation outcome 2b
Effectiveness - The proportion with controlled blood pressure as measured by blood pressure readings taken at the 6 months study visit
Primary quantitative implementation outcome 3a
Adoption - The proportion of clinic encounters in EHR where anti-hypertensive medications are prescribed if indicated, as attainted from EHR proportion of clinic encounters in EHR where 10-year CVD risk is calculated
Primary quantitative implementation outcome 3b
Adoption - The proportion of clinic encounters in EHR where anti-hypertensive medications are prescribed if indicated, as attainted from EHR proportion of clinic encounters in EHR where 10-year CVD risk is calculated
Primary quantitative implementation outcome 3c
Adoption - The proportion of clinic encounters in which 10-year CVD risk is calculated, data obtained from the EHR
Primary quantitative implementation outcome 3d
Adoption - The proportion of clinic encounters in which 10-year CVD risk is calculated, data obtained from the EHR
Co-primary qualitative implementation outcome 1
Fidelity - Audit of intervention implementation as designed as measured by weekly research assistant auditing checklist
Co-primary qualitative implementation outcome 2a
Maintenance - Provider perceptions of ability to maintain plus change in blood pressure control at 12 months as measured by providers qualitative interviews
Co-primary qualitative implementation outcome 2b
Maintenance - Patients perceptions of ability to maintain plus change in blood pressure control at 12 months as measured by patients qualitative interviews

Secondary Outcome Measures

Secondary implementation outcome 1a
Feasibility - The ability to implement integrated HIV/HTN care, HIV/HTN/CVD care, clinic viral suppression as measured by clinics-administered interviews at baseline
Secondary implementation outcome 1b
Feasibility - The ability to implement integrated HIV/HTN care, HIV/HTN/CVD care, clinic viral suppression as measured by clinics-administered interviews at 12 months
Secondary implementation outcome 2a
Acceptability - The patient perception of acceptability of the interCARE intervention package measured by survey and interviews at baseline
Secondary implementation outcome 2b
Acceptability - The provider perception of acceptability of the interCARE intervention package measured by survey and interviews at baseline
Secondary implementation outcome 2c
Acceptability - The provider perception of acceptability of the interCARE intervention package measured by survey and interviews at 12 months
Secondary implementation outcome 2d
Acceptability - The patient perception of acceptability of the interCARE intervention package measured by survey and interviews at 12 months
Exploratory secondary outcomes 3a
Change from baseline in % PLWHIV and HTN screened for any CVD risk factors, data collected from the EHR at 6 months
Exploratory secondary outcomes 3b
Change from baseline in % PLWHIV and HTN screened for any CVD risk factors, data collected from the EHR at 12 months

Full Information

First Posted
May 18, 2022
Last Updated
June 21, 2023
Sponsor
University of Botswana
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1. Study Identification

Unique Protocol Identification Number
NCT05414526
Brief Title
Integrating Hypertension and Cardiovascular Diseases Care Into Existing HIV Services Package in Botswana (InterCARE)
Acronym
InterCARE
Official Title
Integrating Hypertension and Cardiovascular Diseases Care Into Existing HIV Services Package in Botswana (InterCARE)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2020 (Actual)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Botswana

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
The InterCARE research project proposes to leverage a successful national ART program to develop an effective package to improve the uptake of established effective hypertension and CVD risk factors management interventions among PLWHIV in Botswana and other low- and middle-income countries. Being the first project of its kind in Botswana, if successful, the InterCARE package could be readily rolled out to health facilities nationwide to diagnose, treat, track, and support the estimated 25-30% Batswana with hypertension.
Detailed Description
The InterCARE research project is in 2 phases: Phase 1 is a pilot study to refine the 3 interventions mentioned above will take place until November 2022. Clinics staff will receive training on the management of CVD (and hypertension in particular) in-person or online. Attendees feedback will be sought to improve the curriculum prior to being rolled-out in the next phase of this research project. In parallel, the InterCARE Study Team will work with the 2 clinics Information Technology teams to adapt the existing electronic health records with CVD-specific flags, medication lists and laboratory panels. Finally, up to 288 participants (PLWHIV) and their treatment partners will be enrolled from those 2 clinics patients lists to pilot the overall InterCARE package. The results and experiences from the pilot stage will be assessed and collated to make improvements to each of the 3 intervention in the package. This final set of improved interventions will be the basis of the second phase of the InterCARE research project. Phase 1 is anticipated to last until November 2022. The InterCARE package will be tested as a cluster randomised trial in 14 clinics around Botswana: 7 clinics will receive the InterCARE package while the remaining 7 clinics will not received any intervention, continuing with the local standard of care, with a target combined recruitment target of 4652 participants overall, to be followed up for 24 months. Phase 2 is anticipated to take place from January 2023 to July 2025.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Hypertension

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
InterCARE is the name of the package of implementation strategies proposed by the investigators that are intended to integrate cardiovascular care services into existing HIV care systems in Botswana. The InterCARE package includes 3 main interventions: a tailored inter-professional training curriculum on management of CVD risk and HIV adaptation of the existing electronic health records (PIMS) adoption of a treatment partner support system.
Masking
None (Open Label)
Allocation
N/A
Enrollment
288 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
InterCARE package
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
InterCARE package
Intervention Description
The InterCARE package includes: Healthcare Provider HTN/CVD Curriculum A new HTN curriculum will be developed in collaboration with local stakeholders using KITSO Master trainer program documents (Healthcare provider HIV curriculum), Primary Care Guidelines, HTN/CVD curriculum/protocols trialled in Kweneng District and the CDC Prevention Hypertension Management Curriculum. Adaptation of HIV care EHR for HTN/CVD care EHR modifications will be done to enhance data collection around HTN/CVD care, with input from MoH. Patient and treatment partner sessions Clinic staff will provide in-clinic education and counselling on HTN/CVD to all PLWHIV with a diagnosis of hypertension during their routine HIV clinic visit. All patients will be provided a take-home easy-to-read pamphlet on HTN/CVD risk factor management. All PLWHIV will be asked to bring a treatment partner from their social network at the 2nd study visit so that they can practice role-plays with each other.
Primary Outcome Measure Information:
Title
Primary quantitative implementation outcome 1a
Description
Change from baseline in % of patients with HIV who are aware of their hypertension
Time Frame
At 6 months
Title
Primary quantitative implementation outcome 1b
Description
Change from baseline in % of patients with HIV who are aware of their hypertension
Time Frame
At 12 months
Title
Primary quantitative implementation outcome 2a
Description
Effectiveness - The proportion with controlled blood pressure as measured by blood pressure readings taken at the 6 months study visit
Time Frame
At 6 months
Title
Primary quantitative implementation outcome 2b
Description
Effectiveness - The proportion with controlled blood pressure as measured by blood pressure readings taken at the 6 months study visit
Time Frame
At 12 months
Title
Primary quantitative implementation outcome 3a
Description
Adoption - The proportion of clinic encounters in EHR where anti-hypertensive medications are prescribed if indicated, as attainted from EHR proportion of clinic encounters in EHR where 10-year CVD risk is calculated
Time Frame
At 6 months
Title
Primary quantitative implementation outcome 3b
Description
Adoption - The proportion of clinic encounters in EHR where anti-hypertensive medications are prescribed if indicated, as attainted from EHR proportion of clinic encounters in EHR where 10-year CVD risk is calculated
Time Frame
At 12 months
Title
Primary quantitative implementation outcome 3c
Description
Adoption - The proportion of clinic encounters in which 10-year CVD risk is calculated, data obtained from the EHR
Time Frame
At 6 months
Title
Primary quantitative implementation outcome 3d
Description
Adoption - The proportion of clinic encounters in which 10-year CVD risk is calculated, data obtained from the EHR
Time Frame
At 12 months
Title
Co-primary qualitative implementation outcome 1
Description
Fidelity - Audit of intervention implementation as designed as measured by weekly research assistant auditing checklist
Time Frame
Weekly and summative at 12 months
Title
Co-primary qualitative implementation outcome 2a
Description
Maintenance - Provider perceptions of ability to maintain plus change in blood pressure control at 12 months as measured by providers qualitative interviews
Time Frame
At 12 months
Title
Co-primary qualitative implementation outcome 2b
Description
Maintenance - Patients perceptions of ability to maintain plus change in blood pressure control at 12 months as measured by patients qualitative interviews
Time Frame
At 12 months
Secondary Outcome Measure Information:
Title
Secondary implementation outcome 1a
Description
Feasibility - The ability to implement integrated HIV/HTN care, HIV/HTN/CVD care, clinic viral suppression as measured by clinics-administered interviews at baseline
Time Frame
At baseline visit
Title
Secondary implementation outcome 1b
Description
Feasibility - The ability to implement integrated HIV/HTN care, HIV/HTN/CVD care, clinic viral suppression as measured by clinics-administered interviews at 12 months
Time Frame
At 12 months
Title
Secondary implementation outcome 2a
Description
Acceptability - The patient perception of acceptability of the interCARE intervention package measured by survey and interviews at baseline
Time Frame
At baseline
Title
Secondary implementation outcome 2b
Description
Acceptability - The provider perception of acceptability of the interCARE intervention package measured by survey and interviews at baseline
Time Frame
At baseline
Title
Secondary implementation outcome 2c
Description
Acceptability - The provider perception of acceptability of the interCARE intervention package measured by survey and interviews at 12 months
Time Frame
At 12 months
Title
Secondary implementation outcome 2d
Description
Acceptability - The patient perception of acceptability of the interCARE intervention package measured by survey and interviews at 12 months
Time Frame
At 12 months
Title
Exploratory secondary outcomes 3a
Description
Change from baseline in % PLWHIV and HTN screened for any CVD risk factors, data collected from the EHR at 6 months
Time Frame
At 6 months
Title
Exploratory secondary outcomes 3b
Description
Change from baseline in % PLWHIV and HTN screened for any CVD risk factors, data collected from the EHR at 12 months
Time Frame
At 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria for participants: Adults aged 20-75 years old Documented HIV-infection on ART Confirmed diagnosis of hypertension or elevated blood pressure >140/90mmHg versus >130/80mmHg if they have underlying Diabetes Mellitus or Chronic Kidney Disease Receiving regular care at the selected clinics Exclusion Criteria: ● Positive for HIV-related dementia Inclusion criteria for participants' treatment partners: Adults aged 18 years of age or older Selected to be a treatment partner by participant.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mosepele Mosepele, MD
Phone
+26771897691
Email
mosepele.mosepele@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Nabila FJ Youssouf
Email
nabila.youssouf@LSHTM.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mosepele Mosepele, MD
Organizational Affiliation
University of Botswana
Official's Role
Principal Investigator
Facility Information:
Facility Name
Phitsane-Molopo IDCC Clinic
City
Pitsane
Country
Botswana
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matron in charge
Email
none@onfile.bw
Facility Name
Tonota IDCC Clinic
City
Tonota
Country
Botswana
Individual Site Status
Completed

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data recorded as part of the study will be anonymised and will be deposited in a secured archiving facility at the University of Botswana Health Records Unit. Researchers may request access to data as part of transparency and data sharing however this is strictly upon request and will be governed through the required legal office, with at the least, a Data Sharing Agreement in place. Further details on this can be found in our Data Management plan.

Learn more about this trial

Integrating Hypertension and Cardiovascular Diseases Care Into Existing HIV Services Package in Botswana (InterCARE)

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