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Integrating Family Planning Services Into HIV Care and Treatment in Nyanza Province, Kenya

Primary Purpose

Unintended Pregnancy, HIV Infections

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Integrated family planning/HIV care and treatment services
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Unintended Pregnancy focused on measuring Family planning, HIV, Integrated services, Unintended pregnancy, Kenya

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

For health facilities:

  • Each site must be providing HIV care and treatment services

For participants:

  • Women aged 18-45, not pregnant, HIV+, receiving HIV care at that health facility
  • Men aged 18 and above, HIV+, receiving HIV care at that health facility

Exclusion Criteria:

For health facilities

  • If they do not meet the inclusion criteria listed above
  • If they are already providing integrated comprehensive HIV care and treatment that includes on-site family planning counseling and provision

For participants:

  • Participants are excluded if they do not meet the inclusion criteria listed above.

Sites / Locations

  • Migori District Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Integrated HIV/FP services

Standard (non-integrated), referral-based, services

Arm Description

Family planning services are integrated into HIV care and treatment services at this facility.

Patients from the HIV care and treatment clinic will be referred for family planning services, and will not receive FP services by the HIV care provider

Outcomes

Primary Outcome Measures

Prevalence More Effective Contraception (defined as hormonal methods, intrauterine devices, and permanent methods)
Pregnancy rate

Secondary Outcome Measures

Knowledge of contraceptive methods among HIV-positive women
Knowledge of contraceptive methods among providers
Acceptability of family planning services
Feasibility of providing family planning services at HIV care and treatment centers
Reproductive intentions of HIV-infected women receiving care and treatment

Full Information

First Posted
October 22, 2009
Last Updated
December 6, 2013
Sponsor
University of California, San Francisco
Collaborators
Ibis Reproductive Health, Kenya Medical Research Institute, Tides, Bill and Melinda Gates Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01001507
Brief Title
Integrating Family Planning Services Into HIV Care and Treatment in Nyanza Province, Kenya
Official Title
Cluster Randomized Trial of Integration of Family Planning Services Into HIV Care and Treatment in Suba, Kisumu East, Rongo and Migori Districts of Nyanza Province
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
October 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Ibis Reproductive Health, Kenya Medical Research Institute, Tides, Bill and Melinda Gates Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a cluster randomized trial comparing the integration of family planning services into HIV care and treatment programs versus the standard referral for family planning services outside of HIV care and treatment programs within Suba, Kisumu East, Rongo and Migori districts in Nyanza province.
Detailed Description
The study will have three parts. During the first part (3 months), baseline data on contraceptive prevalence and unintended pregnancy will be collected at 18 PSCs that are supported by the FACES program in Suba, Kisumu East, Nyatike, Rongo and Migori Districts. Also during this first part, information about knowledge, attitudes and practices related to family planning will be obtained from patients and from clinicians at the sites. During the second part (3 months), an intervention consisting of integrating family planning services will be designed and implemented at twelve of the 18 FACES-supported PSCs. We aim to utilize a 2:1 integration:control model, with delayed integration so as to gradually expand the integration of FP and HIV services throughout the 18 sites, while maintaining the ability to test hypotheses on the effects of integration on health outcomes. After collecting the baseline data, we plan to stratify the clinics into two categories based on the overall patient volume and differences in the structure of family planning provision, i.e., whether or not there is a specific MCH division providing family planning at the site or not. Randomization of sites will then occur among clinics in each of these strata, with a ratio of two intervention sites (integrated model) to one control site (family planning provided in the standard manner at the site). During the third and last part (12 months), data on prevalence more effective contraception and unintended pregnancy will be collected from each of the 18 sites. At the end of part three, information about knowledge, attitudes and practices related to family planning again will be obtained from patients and from clinicians at the sites. In addition, we will administer questionnaires assessing the acceptability of family planning services to patients, and in addition clinic staff will be answer a questionnaire assessing the feasibility of providing integrated family planning services. After 12 months of data collection, the 6 control sites were integrated and data were collected for an additional 11 months from all 18 sites to assess the sustainability of the intervention under the Ministry of Health. The study population will primarily consist of HIV-positive men and non-pregnant, HIV-positive women of reproductive age who obtain care at the FACES-supported PSCs in Suba, Kisumu East, Rongo and Migori Districts in Nyanza Province, Kenya. In addition, study subjects will also include clinic staff at the FACES centers included in the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unintended Pregnancy, HIV Infections
Keywords
Family planning, HIV, Integrated services, Unintended pregnancy, Kenya

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5040 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Integrated HIV/FP services
Arm Type
Experimental
Arm Description
Family planning services are integrated into HIV care and treatment services at this facility.
Arm Title
Standard (non-integrated), referral-based, services
Arm Type
No Intervention
Arm Description
Patients from the HIV care and treatment clinic will be referred for family planning services, and will not receive FP services by the HIV care provider
Intervention Type
Procedure
Intervention Name(s)
Integrated family planning/HIV care and treatment services
Intervention Description
Family planning services will be provided during the patient's HIV care visit.
Primary Outcome Measure Information:
Title
Prevalence More Effective Contraception (defined as hormonal methods, intrauterine devices, and permanent methods)
Time Frame
1 year post integration/site initiation and 2 years post integration/site initiation
Title
Pregnancy rate
Time Frame
1 year post integration/study initiation and 2 years post integration/site initiation
Secondary Outcome Measure Information:
Title
Knowledge of contraceptive methods among HIV-positive women
Time Frame
baseline (months 1-3); post-intervention (months 9-12)
Title
Knowledge of contraceptive methods among providers
Time Frame
baseline (months 1-3); post-intervention (months 9-12)
Title
Acceptability of family planning services
Time Frame
baseline (months 1-3); post-intervention (months 9-12)
Title
Feasibility of providing family planning services at HIV care and treatment centers
Time Frame
months 9-12
Title
Reproductive intentions of HIV-infected women receiving care and treatment
Time Frame
months 1-3

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: For health facilities: Each site must be providing HIV care and treatment services For participants: Women aged 18-45, not pregnant, HIV+, receiving HIV care at that health facility Men aged 18 and above, HIV+, receiving HIV care at that health facility Exclusion Criteria: For health facilities If they do not meet the inclusion criteria listed above If they are already providing integrated comprehensive HIV care and treatment that includes on-site family planning counseling and provision For participants: Participants are excluded if they do not meet the inclusion criteria listed above.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Craig Cohen, MD, MPH
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Daniel Grossman, MD
Organizational Affiliation
Ibis Reproductive Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Elizabeth Bukusi, MBChB, PhD
Organizational Affiliation
Kenya Medical Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sara Newmann, MD, MPH
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
Migori District Hospital
City
Migori
Country
Kenya

12. IPD Sharing Statement

Citations:
PubMed Identifier
28328966
Citation
Cohen CR, Grossman D, Onono M, Blat C, Newmann SJ, Burger RL, Shade SB, Bett N, Bukusi EA. Integration of family planning services into HIV care clinics: Results one year after a cluster randomized controlled trial in Kenya. PLoS One. 2017 Mar 22;12(3):e0172992. doi: 10.1371/journal.pone.0172992. eCollection 2017.
Results Reference
derived

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Integrating Family Planning Services Into HIV Care and Treatment in Nyanza Province, Kenya

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