NCT05211531

Brief Summary

Program studying the number of steps post-operative patients need to take to prevent post-operative complications. Also studying surgical resident wellness program that provides extra time to ambulate with inpatients.

Trial Health

57
Monitor

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2021

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
terminated

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2021

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

January 11, 2022

Completed
16 days until next milestone

First Posted

Study publicly available on registry

January 27, 2022

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 25, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 25, 2022

Completed
Last Updated

September 25, 2024

Status Verified

September 1, 2024

Enrollment Period

11 months

First QC Date

January 11, 2022

Last Update Submit

September 23, 2024

Conditions

Keywords

Resident physician wellnessPost-operative walking program

Outcome Measures

Primary Outcomes (2)

  • Total number of steps

    Total number of steps ambulated by the patient as measured by a pedometer

    From index surgery to initial post-operative office visit, up to 3 weeks

  • 30 day Post-operative complications

    30 day Post-operative complications

    30 days

Interventions

Measuring the number of post-operative steps that inpatients take.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Minimally invasive surgery patients who are admitted and undergo surgery at a single tertiary care center.

You may qualify if:

  • Post-operative surgical patient with an over 24 hour post-operative stay in the hospital
  • Safe to ambulate with/without assistance

You may not qualify if:

  • Unable to ambulate
  • Bedbound

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UMASS Memorial Medical Center

Worcester, Massachusetts, 01655, United States

Location

Study Officials

  • Richard Perugini, MD

    UMASS Memorial Healthcare

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

January 11, 2022

First Posted

January 27, 2022

Study Start

August 1, 2021

Primary Completion

June 25, 2022

Study Completion

June 25, 2022

Last Updated

September 25, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations