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Community-based Provision of Urine Pregnancy Tests as Linkage to Reproductive Health Services

Primary Purpose

Prenatal Care Late, Contraceptive Usage, Pregnancy Complication

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Urine Pregnancy Test
CHV-based post-test counseling & referral
Phone-based post-test counseling & referral
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prenatal Care Late

Eligibility Criteria

15 Years - 45 Years (Child, Adult)FemaleAccepts Healthy Volunteers

CHV participants:

Inclusion:

  • Approved and designated CHV by their respective county
  • Has been in their role for at least 1 year Exclusion: if they do not meet the inclusion criteria

Women participants:

Inclusion Criteria:

  • Women aged 15-45, inclusive
  • Desire to use a urine pregnancy test for any reason.
  • Have availability of a phone.
  • Agree to enrollment in the study and to be contacted for data collection
  • Conversant in Kiswahili or English

Exclusion Criteria:

• Physical or mental illness that precludes study involvement

Sites / Locations

  • Moi University/MTRH

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

CHV-provided post-test counseling & referral

Phone-based post-test counseling & referral

Arm Description

The CHV will provide the woman with the urine pregnancy test and collect baseline information. If the woman desires enrollment in Arm 1 (CHV-provided post-test counseling and referral), the CHV will provide all post-test counseling and referral based on training provided. This may occur at the time of enrollment or at a later time, as preferred by the woman.

The CHV will provide the woman with the urine pregnancy test and collect baseline information. If the woman desires enrollment in Arm 2 (phone-based post-test counseling and referral), the CHV will provide the woman with a phone number which she may call or short message service (SMS) to receive post-test counseling and referral. If the study team does not receive a call or SMS from the woman within one week, our research assistant will phone and/or SMS the participant to provide phone-based post-test counseling and referral.

Outcomes

Primary Outcome Measures

Utilization of care
Defined as proportion of participants who self-report attendance to at least one Antenatal Care (ANC) visit for women with positive UPT or Family Planning (FP) clinic visit for women with negative UPT

Secondary Outcome Measures

Participant Satisfaction with CHV-based UPT provision
Participant self-report of satisfaction with CHV-based UPT provision on scale of very unsatisfied to very satisfied
Participant preference for CHV-based vs phone-based post-test counseling and referral
Proportion of participants who choose CHV-based vs. phone-based post-test counseling and referral
Number of UPTs provided per month
CHV self-report of total number of UPTs provided per month (including participants & women who declined enrollment or did not meet inclusion criteria)
CHV comfort with UPT provision and post-test counseling and referral
CHV self-report of of comfort with UPT provision and post-test counseling and referral on a scale from not comfortable to very comfortable
Participant utilization of phone-based post-test counseling and referral
Proportion of participants who call/SMS and respond to call/SMS for phone-based post-test counseling and referral
Results of UPTs
Proportion of negative vs. positive UPT results
Gestational age at first ANC visit
Participant self-report of gestational age at first ANC visit for women with positive UPT who attended ANC visit (reported as mean and range)
initiation of FP and method of FP
Participant self-report of initiation of family planning and method of family planning initiated (reported as proportion of women with negative UPT who initiated FP and proportion initiating each method of FP)

Full Information

First Posted
July 29, 2018
Last Updated
March 18, 2020
Sponsor
Indiana University
Collaborators
Moi University
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1. Study Identification

Unique Protocol Identification Number
NCT03626597
Brief Title
Community-based Provision of Urine Pregnancy Tests as Linkage to Reproductive Health Services
Official Title
Community-based Provision of Urine Pregnancy Tests as Linkage to Reproductive Health Services
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
October 13, 2018 (Actual)
Primary Completion Date
September 1, 2019 (Actual)
Study Completion Date
November 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Moi University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Kenyan families experience persistently high rates of maternal and neonatal mortality, which disproportionately affects women with low income and education and those who live far from health services. Key proven interventions include prevention of pregnancy and birth spacing, early entry to antenatal care, and facility delivery. However, creative, cost-effective interventions are urgently needed to link particularly vulnerable populations with these important health services. Previous research has shown that equipping community health volunteers (CHVs) with a tool as simple as a urine pregnancy test and training to provide post-test counseling is effective in improving linkages to antenatal care and family planning services. The invesitgators' proposal includes a multi-phase process to collect qualitative data through a needs assessment (Phase 1), use community input to develop (Phase 2) and implement a pilot intervention study (Phase 3) assessing the ability of CHV-based provision of urine pregnancy tests with CHV-provided and phone-based post-test counseling to link women with antenatal care and family planning services, and collect qualitative program evaluation data (Phase 4). This will provide much-needed information for how to effectively utilize and strengthen CHVs as part of a sustainable reproductive health care delivery system to improve maternal and neonatal mortality. The broad objectives are to determine whether the use of community-based provision of urine pregnancy tests with post-test counseling and referral to care is acceptable to community health volunteers (CHVs) and participants and to determine which method of post-test counseling and referral to care, CHV-provided or phone-based, is more acceptable and more effective. Participant outcomes, including the primary outcome of utilization of ANC or family planning care, will be measured by telephone questionnaires one to three months post-enrollment. CHV outcomes will be determined by telephone questionnaires as well as review of CHV log books.
Detailed Description
Kenyan families experience persistently high rates of maternal and neonatal morbidity and mortality, which disproportionately affects women with low educational attainment and income and those who live far from health services. Key proven interventions include prevention of pregnancy and birth spacing, early entry to antenatal care, and facility delivery. However, creative, cost-effective interventions are urgently needed to link particularly vulnerable populations with these important health services. Previous research has shown that equipping community health volunteers with a tool as simple as a urine pregnancy test and training to provide post-test counseling is effective in improving linkages to antenatal care and family planning services. The investigators' proposal includes a multi-phase process to collect qualitative data through a needs assessment, use community input to develop and implement a pilot study assessing the ability of CHV-based provision of urine pregnancy tests with CHV-provided and phone-based post-test counseling to link women with antenatal care and family planning services, and collect qualitative program evaluation data. This will provide much-needed information for how to effectively utilize and strengthen CHVs as part of a sustainable reproductive health care delivery system to improve maternal and neonatal mortality. Expected outcomes include important qualitative data regarding the needs and preferences of women and CHVs to improve reproductive health services. Additionally, the investigators will perform a quantitative comparison of CHV-provided and phone-based post-test counseling to inform further research projects and CHV services. The investigators will plan to publish this clinical research in international peer-reviewed journals and to host community events to share the results of the study. The investigators anticipate that the outcomes from this pilot research will allow them to apply for research funding for expansion of this intervention throughout the catchment area to evaluate its effects on key population health outcomes, including maternal and neonatal mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prenatal Care Late, Contraceptive Usage, Pregnancy Complication

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel, non-blinded, patient preference model.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
308 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CHV-provided post-test counseling & referral
Arm Type
Active Comparator
Arm Description
The CHV will provide the woman with the urine pregnancy test and collect baseline information. If the woman desires enrollment in Arm 1 (CHV-provided post-test counseling and referral), the CHV will provide all post-test counseling and referral based on training provided. This may occur at the time of enrollment or at a later time, as preferred by the woman.
Arm Title
Phone-based post-test counseling & referral
Arm Type
Active Comparator
Arm Description
The CHV will provide the woman with the urine pregnancy test and collect baseline information. If the woman desires enrollment in Arm 2 (phone-based post-test counseling and referral), the CHV will provide the woman with a phone number which she may call or short message service (SMS) to receive post-test counseling and referral. If the study team does not receive a call or SMS from the woman within one week, our research assistant will phone and/or SMS the participant to provide phone-based post-test counseling and referral.
Intervention Type
Diagnostic Test
Intervention Name(s)
Urine Pregnancy Test
Intervention Description
CHV will provide all participants with in-person urine pregnancy tests (UPTs)
Intervention Type
Behavioral
Intervention Name(s)
CHV-based post-test counseling & referral
Intervention Description
CHVs will provide in-person post-test counseling & referral to care
Intervention Type
Behavioral
Intervention Name(s)
Phone-based post-test counseling & referral
Intervention Description
Participants will call/SMS or be called/SMSed for phone-based counseling & referral to care
Primary Outcome Measure Information:
Title
Utilization of care
Description
Defined as proportion of participants who self-report attendance to at least one Antenatal Care (ANC) visit for women with positive UPT or Family Planning (FP) clinic visit for women with negative UPT
Time Frame
1-3 months post-enrollment
Secondary Outcome Measure Information:
Title
Participant Satisfaction with CHV-based UPT provision
Description
Participant self-report of satisfaction with CHV-based UPT provision on scale of very unsatisfied to very satisfied
Time Frame
1-3 months post-enrollment
Title
Participant preference for CHV-based vs phone-based post-test counseling and referral
Description
Proportion of participants who choose CHV-based vs. phone-based post-test counseling and referral
Time Frame
At the time of enrollment
Title
Number of UPTs provided per month
Description
CHV self-report of total number of UPTs provided per month (including participants & women who declined enrollment or did not meet inclusion criteria)
Time Frame
Monthly, thoughout the study period (estimated 10 months)
Title
CHV comfort with UPT provision and post-test counseling and referral
Description
CHV self-report of of comfort with UPT provision and post-test counseling and referral on a scale from not comfortable to very comfortable
Time Frame
At the time of time of UPT provision
Title
Participant utilization of phone-based post-test counseling and referral
Description
Proportion of participants who call/SMS and respond to call/SMS for phone-based post-test counseling and referral
Time Frame
1-3 months post-enrollment
Title
Results of UPTs
Description
Proportion of negative vs. positive UPT results
Time Frame
1-3 months post-enrollment
Title
Gestational age at first ANC visit
Description
Participant self-report of gestational age at first ANC visit for women with positive UPT who attended ANC visit (reported as mean and range)
Time Frame
1-3 months post-enrollment
Title
initiation of FP and method of FP
Description
Participant self-report of initiation of family planning and method of family planning initiated (reported as proportion of women with negative UPT who initiated FP and proportion initiating each method of FP)
Time Frame
1-3 months post-enrollment

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Participants must self-represent as female
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
CHV participants: Inclusion: Approved and designated CHV by their respective county Has been in their role for at least 1 year Exclusion: if they do not meet the inclusion criteria Women participants: Inclusion Criteria: Women aged 15-45, inclusive Desire to use a urine pregnancy test for any reason. Have availability of a phone. Agree to enrollment in the study and to be contacted for data collection Conversant in Kiswahili or English Exclusion Criteria: • Physical or mental illness that precludes study involvement
Facility Information:
Facility Name
Moi University/MTRH
City
Eldoret
ZIP/Postal Code
30100
Country
Kenya

12. IPD Sharing Statement

Plan to Share IPD
No

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Community-based Provision of Urine Pregnancy Tests as Linkage to Reproductive Health Services

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