ClinicalTrials.gg
CompletedNCT01854671Updated Aug 17, 2015

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

An interventional study of family planning counseling let by community health workers in Focus: Contraceptive Counseling and Focus: Postpartum Contraception, sponsored by Planned Parenthood League of Massachusetts. Completed at 1 site in Palestinian Territories. Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-08-17.

Sponsored by Planned Parenthood League of Massachusetts · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
176
Allocation
Non-randomized
Sex
Female
01

Study 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.

02

Conditions studied

  • Focus: Contraceptive Counseling
  • Focus: Postpartum Contraception

Keywords

  • postpartum contraception
  • contraceptive counseling
03

In context

Lead sponsor

Planned Parenthood League of Massachusetts is the lead sponsor of 17 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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
05

Study design

Phase
Not applicable
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
176 participants (actual)

Study arms

  • No intervention
    standard care
  • Experimental
    family planning counseling led by community health worker

    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.

    Other: family planning counseling let by community health workers

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.

06

What researchers measure

Primary outcomes

  1. Self-reported contraceptive use

    Time frame: 6 months post-partum

Secondary outcomes

  1. Intent to use contraception in the future

    Time frame: 6 months postpartum

  2. Non-desire to use contraception

    Time frame: 6 months postpartum

07

Study locations

1 site
  • Palestinian Ministry of Health Maternal Child Health Clinics (Ramallah and Al-Bireh)
    Ramallah and Al-Bireh, West Bank, Palestinian Territories
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Aug 2013, a primary completion of Dec 2014 and a completion of Dec 2014. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
May 13, 2013
First posted
May 15, 2013
Start
Aug 2013
Primary completionActual
Dec 2014
CompletionActual
Dec 2014
Last update
Aug 17, 2015
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 17, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01854671
Lead sponsor
Planned Parenthood League of Massachusetts
Collaborators
Society for Family Planning Research Fund
Responsible party
Sponsor
First posted
May 15, 2013
Start date
Aug 2013
Primary completion
Dec 2014
Completion
Dec 2014
Last update
Aug 17, 2015

Study contacts

Principal Investigator, MD, MPH
principal investigator · Planned Parenthood League of Massachusetts

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2015. You cannot join it, but the record below documents what was studied.

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