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Evaluation of Patient-Reported Outcomes Measurement Information System (PROMIS)-29 v2.1 for Postpartum Women

Evaluation of Patient-Reported Outcomes Measurement Information System (PROMIS)-29 v2.1 for Postpartum Women

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06002763
Enrollment
200
Registered
2023-08-21
Start date
2025-07-09
Completion date
2026-07-31
Last updated
2025-07-15

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

Conditions

Well-Being, Psychological

Keywords

cesarean delivery, vaginal delivery, postpartum recovery

Brief summary

There is no widely used, statistically validated assessment for physical and mental health for the short- to medium-term in a postpartum population. PROMIS-29 has been validated for the assessment of these factors in a generic population, but has not been specifically evaluated for use with postpartum women. This study is a longitudinal, single center observational cohort study designed to evaluate the reliability of the Patient-Reported Outcomes Measurement Information System (PROMIS)-29 v2.1 survey in a postpartum population. PROMIS-29 is a survey designed to screen for pain, impairments in mood, physical function, and activities of daily living. While this survey has shown utility in other populations, it has yet to be assessed in an obstetric population. The investigators plan to recruit patients who are recently postpartum from vaginal or cesarean delivery to complete virtual surveys at defined time points (0, 2, 6, and 12 weeks after delivery). The investigators will subject survey data to statistical measures of validity and reliability comparing with contemporaneously collected surveys of established metrics for quality of life (WHOQoLBREF) and general (global) state of health (numerical rating score 1-100). The hypothesis is that the PROMIS-29 v2.1 questionnaire is a statistically valid and reliable means of assessing physical and mental health in a postpartum population.

Interventions

OTHERPROMIS-29 v2.1 (Patient-Reported Outcomes Measurement Information System)

PROMIS-29 is a survey designed to screen for pain, impairments in mood, physical function, and activities of daily living.

OTHERWHOQoLBREF (World Health Organization Quality of Life Brief Version)

The WHOQOL-BREF is a 26-item version of the 100-item WHOQOL-100 quality of life measure that addresses four quality of life domains: physical health, psychological health, social relationships and environment.

OTHEREQ-5D-3L1 (not an acronym)

The EQ-5D-3L1 is a generic measure of health status consisting of two parts. The first part assesses health in five dimensions: MOBILITY, SELFCARE, USUAL ACTIVITIES, PAIN / DISCOMFORT, ANXIETY/DEPRESSION. The second part of the questionnaire consists of a VAS on which the patient rates their perceived health from 0 (the worst imaginable health) to 100 (the best imaginable health).

Sponsors

Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* 18 years old and over * singleton births * 37 or more weeks gestational age * multiparous or nulliparous patients * spontaneous vaginal delivery or scheduled cesarean delivery with labor analgesia or neuraxial anesthesia * give informed written consent

Exclusion criteria

* refusal to take part * are unable to give or have withdrawn consent * patients unable to communicate fluently in English * patients who are less than 18 years old * patients who had fetal demise or severely morbid fetal conditions such as intubation, cooling, expected surgical correction of congenital anomaly during hospitalization (although NICU admissions will be included) * patients who were admitted in ICU * patients who had failed neuraxial analgesia such as replaced epidurals or failed spinal requiring conversion to general anesthesia * patients who had general anesthesia for cesarean delivery as defined by GETA, including sedatives and deep sedation if not intubated * patients who had intrapartum cesarean or had assisted/operative (i.e. vacuum, forceps) vaginal delivery.

Design outcomes

Primary

MeasureTime frameDescription
PROMIS-29 v2.1 (Patient-Reported Outcomes Measurement Information System) survey score24 hoursThe PROMIS survey score at 24 hours postpartum
WHOQoLBREF (World Health Organization Quality of Life Brief Version) survey score24 hoursThe WHOQoLBREF survey score at 24 hours postpartum
EQ-5D-3L1 (not an acronym) survey score24 hoursThe EQ-5D-3L1 survey score at 24 hours postpartum

Countries

Canada

Contacts

Primary ContactRonald George, MD
ron.george@uhn.ca416-586-4800

Outcome results

None listed

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