Philadelphia Preterm Prevention Project

NACompletedINTERVENTIONAL
Enrollment

1,136

Participants

Timeline

Start Date

November 30, 2004

Primary Completion Date

August 31, 2008

Study Completion Date

September 30, 2008

Conditions
Preterm Birth
Interventions
OTHER

Psychological intervention

Subjects will be randomized into either usual care or interconceptional intervention groups. If the subject is randomized into the intervention group, she will receive targeted interventions to reduce one of several risk factors: smoking, depression, infectious disease burden and maternal stress, and achieving an appropriate BMI. A woman who is randomized to the intervention group may receive interventions on one, two, three, four, or five of the targeted intervention methods, depending on her needs.

OTHER

Usual Care Group

Trial Locations (1)

19104

Children's Hospital of Philadelphia, Philadelphia

All Listed Sponsors
lead

Children's Hospital of Philadelphia

OTHER

NCT01117922 - Philadelphia Preterm Prevention Project | Biotech Hunter | Biotech Hunter