NCT02432573

Brief Summary

In postpartum hospitalized women, does delayed morning rounding improve patient satisfaction?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started May 2015

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 9, 2015

Completed
22 days until next milestone

Study Start

First participant enrolled

May 1, 2015

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 4, 2015

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2015

Completed
Last Updated

February 12, 2016

Status Verified

February 1, 2016

Enrollment Period

2 months

First QC Date

April 9, 2015

Last Update Submit

February 11, 2016

Conditions

Physician RoundsPostpartum

Keywords

timing

Outcome Measures

Primary Outcomes (1)

  • score on Hospital Consumer Assessment of Healthcare Provers and Systems (HCAPS) survey

    Patient will be give a modified version of the validated HCAPS survey at discharge from the hospital to assess patient satisfaction and the scores will be compared between the 2 groups.

    2 months

Secondary Outcomes (1)

  • score on Edinburgh Postnatal Depression Scale

    2 months

Study Arms (2)

Standard care

NO INTERVENTION

Postpartum patients that receive physician rounding at current time

Delayed rounding

EXPERIMENTAL

Postpartum patients that receive physician rounding at a delayed time

Behavioral: Delayed rounds

Interventions

Delayed roundsBEHAVIORAL
Delayed rounding

Eligibility Criteria

Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Delivered between 0600 and 0000
  • Admitted to Memorial Hermann postpartum unit
  • Patient managed by the University of Texas Physicians Group and/or obstetrics-gynecology residents

You may not qualify if:

  • \- None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Texas Medical Center, Memorial Hermann Hospital

Houston, Texas, 77030, United States

Location

Related Publications (1)

  • Roberts RP, Blackwell SC, Brown KM, Pedroza C, Sibai BM, Tyson JE. Early Compared With Delayed Physician Rounds on Patient Satisfaction of Postpartum Women: A Randomized Controlled Trial. Obstet Gynecol. 2016 Aug;128(2):381-386. doi: 10.1097/AOG.0000000000001528.

    PMID: 27400002DERIVED

Study Officials

  • Robyn P Roberts, MD

    University of Texas

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Fellow

Study Record Dates

First Submitted

April 9, 2015

First Posted

May 4, 2015

Study Start

May 1, 2015

Primary Completion

July 1, 2015

Study Completion

July 1, 2015

Last Updated

February 12, 2016

Record last verified: 2016-02

Locations

US(1)