Mode
Text Size
Log in / Sign up
N/A N=1,144 Randomized Health Services Research

Involving Men in Maternity Care in Burkina Faso

Postpartum Period

Enrolled (actual)
1,144
Serious AEs
0.0%
Results posted
Jul 2019
Primary outcome: Primary: Number of Participants Attending the Recommended Number of Postnatal Care Appointments — 342; 265 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Partner involvement (Behavioral)
Age
Pediatric, Adult, Older Adult · 16+ yrs
Sex
Female
Sponsor
London School of Hygiene and Tropical Medicine
Primary completion
Jul 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Attending the Recommended Number of Postnatal Care Appointments
342; 265
PRIMARY
Number of Participants Practicing Exclusive Breastfeeding at 3 Months Postpartum
232; 161
PRIMARY
Number of Participants Using Effective Modern Contraception at 8 Months Postpartum
330; 283
SECONDARY
Number of Participants Using Long Acting or Permanent (LA/PM) Methods of Contraception at 8 Months Postpartum
170; 122
SECONDARY
Number of Participants Using Any Contraceptive Method at 8 Months Postpartum
391; 343
SECONDARY
Number of Participants Who Initiated Postpartum Contraception in a Timely Fashion
249; 188
SECONDARY
Number of Participants With an Unmet Need for Contraception at 8 Months Postpartum
79; 101
SECONDARY
Number of Participants With High Relationship Adjustment at 8 Months Postpartum
323; 263

Summary

The uptake of postpartum contraception, postpartum care attendance and the practice of exclusive breastfeeding are low in Sub-Saharan Africa. Although the involvement of men in maternity care has been shown to be a promising strategy for the achievement of other reproductive health goals, little is known about the effect of their participation on these outcomes. This study aims to test whether the involvement of men can improve care-seeking and promote healthy behaviours among postpartum women in Burkina Faso.

Eligibility Criteria

Inclusion Criteria

  • Age 16-18, married, or
  • Age 18+, in a co-habiting relationship
  • Pregnant 24-36 weeks
  • No obstetric risk factors requiring hospital delivery
  • Lives no more than one hour away on foot, not planning to move from the city
  • Gives informed consent

Exclusion Criteria

  • Not meeting inclusion criteria
  • Declines to participate
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02309489). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search