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The Periviable Birth Plan

Albany Medical College logo

Albany Medical College

Status

Unknown

Conditions

PreTerm Birth
PTSD
Parturition Complication as Antepartum Condition
Pregnancy, High Risk
Anxiety

Treatments

Behavioral: Periviable Birth Plan

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Pregnant women who are at risk of delivering their infants in the periviable period can suffer a large amount of stress and anxiety. Moreover, many women feel a loss of control over their own pregnancy. There is some evidence that more counseling and planning can help reduce maternal stress and anxiety. Patients at risk of delivering in the periviable period will be randomized to either receive standard counselling or to complete the periviable birth plan.

Enrollment

54 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years old.
  • Currently Pregnant
  • High risk of pre-term birth in the periviable period 20+0 to 25+6 wga

Exclusion criteria

  • Intrauterine Fetal Demise (prior to admission)
  • Inability to read or communicate in english

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 2 patient groups

Standard Counseling
No Intervention group
Description:
Patients at risk of delivery between 20 and 25+6 weeks gestation will receive the normal counseling from Ob/gyn and Neonatology.
Periviable Birth Plan
Experimental group
Description:
Patients at risk of delivery between 20 and 25+6 weeks gestation will receive the normal counseling from Ob/gyn and Neonatology with completion of the written periviable birth plan.
Treatment:
Behavioral: Periviable Birth Plan

Trial contacts and locations

1

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Central trial contact

Paul Burcher, MD; Devon Jacobson, MD

Data sourced from clinicaltrials.gov

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