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Investigating the Effect of a Prenatal Family Planning Counseling Intervention Led by Community Health Workers on Postpartum Contraceptive Use Among Women in the West Bank

Investigating the Effect of a Prenatal Family Planning Counseling Intervention Led by Community Health Workers on Postpartum Contraceptive Use Among Women in the West Bank

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01854671
Enrollment
176
Registered
2013-05-15
Start date
2013-08-31
Completion date
2014-12-31
Last updated
2015-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Focus: Contraceptive Counseling, Focus: Postpartum Contraception

Keywords

postpartum contraception, contraceptive counseling

Brief summary

The purpose of this study is to measure the difference in proportion of postpartum women using contraception after a Community Health Worker (CHW) family planning educational intervention compared to women who receive standard care in the West Bank district of Ramallah and Al-Bireh. Primary hypothesis: Postpartum contraceptive use will increase in women who receive a dedicated family planning counseling intervention delivered by CHWs during antenatal care compared to women receiving usual care.

Interventions

OTHERfamily planning counseling let by community health workers

The family planning counseling sessions led by community health workers will present advantages of birth spacing, available methods of postpartum contraception, contraindications (if any) for the method, when each method can be safely started postpartum, where each method can be obtained, and importance of 6 week postpartum clinic follow-up. There will also be a take-home contraceptive method brochure given at conclusion of information session -primarily pictorial and in Arabic, to facilitate discussion at home with husbands and family members.

Sponsors

Society for Family Planning Research Fund
CollaboratorUNKNOWN
Planned Parenthood League of Massachusetts
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Women attending the MoH Ramallah or Al-Bireh clinic for antenatal care and 34-38 weeks pregnant at enrollment * Planning delivery at an MoH hospital * Able and willing to be contacted by phone or home visit

Exclusion criteria

* Women less than 34 weeks pregnant or non-pregnant * Planning delivery at a private or NGO hospital * Unwilling to be contacted for follow-up after enrollment

Design outcomes

Primary

MeasureTime frame
Self-reported contraceptive use6 months post-partum

Secondary

MeasureTime frame
Intent to use contraception in the future6 months postpartum
Non-desire to use contraception6 months postpartum

Countries

Palestinian Territories

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026