- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02447913
Integrating Family Planning With Immunization to Improve Maternal and Child Health
To Observe the Effectiveness of a Demand-Side Financing Project in Increasing Demand and Utilization of Contraceptives for Birth Spacing Among Women From Poorest Two Quintiles in Faisalabad District of Pakistan
Study Overview
Detailed Description
Study hypothesis: Contraceptive Prevalence Rate will increase up to 20% from the baseline to end line survey in the intervention area .Contraceptive Prevalence Rate will increase by 5% between baseline and end line survey in the control area.
Ethics approval: The study has been approved by Population Services International Research Ethics Board.
Study design: This is a quasi experimental design. The study is a single center.
Primary study design: Interventional Trial setting: Community. Interventions: Introduction of vouchers will improve uptake of family method as well as child immunization.
Incentivizing the providers to improve their counseling skills will improve the provider client relationship and better compliance of Family planning method.
Intervention Type: Behavioral Primary outcome measures: Number of women who took up modern, reversible contraceptive methods ,number of women who availed postnatal care and number of women whose infants were immunized among the two poorest quintiles.
Secondary outcome measures: Improve the quality of family planning service provision in private sector health facilities serving low-income women.
Eligibility
Participant inclusion criteria - Participant type: Other. Participant inclusion criteria - Description: Women who are married in their reproductive age group i-e 15 to 49 years and who have given birth to a child within past one month.
Participant inclusion criteria - Target number of participants: 28000. Participant exclusion criteria: Women who are not married and are not in their reproductive age group i-e 15-49 years and who has not given birth within past 1 month.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Zahid Memon
- Phone Number: +923085550859
- Email: zahidmemon@greenstar.org.pk
Study Contact Backup
- Name: Wajiha Javed
- Email: wajihajaved@greenstar.org.pk
Study Locations
-
-
Punjab
-
Faisalabad, Punjab, Pakistan
- Recruiting
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Women who are married in their reproductive age group i-e 15 to 19 years and who have given birth to a child within past one month
Exclusion Criteria:
- Women who are not married and are not in their reproductive age group i-e 15-49 years and who has not given birth within past 1 month
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
|
|
Experimental: Voucher
|
Introduction of vouchers will improve uptake of family method as well as child immunization. Incentivizing the providers to improve their counseling skills will improve the provider client relationship and better compliance of Family planning method |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
number of women who used modern,reversible contraceptive methods
Time Frame: 2-3 years
|
2-3 years
|
number of women who had postnatal care
Time Frame: 2-3 years
|
2-3 years
|
number of women whose infants had immunizations
Time Frame: 2-3years
|
2-3years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Improve the quality of family planning service provision in private sector health facilities as judged by client satisfaction criteria
Time Frame: 2-3 years
|
2-3 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Zahid Memon, Greenstar Social Marketing
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Grant #2011-37081
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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