NCT06698315

Brief Summary

The project aims to promote patient safety and quality care by reducing preventable falls and falls with injuries using an evidence-based solution.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

July 23, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

November 18, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

November 20, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2025

Completed
Last Updated

November 20, 2024

Status Verified

August 1, 2024

Enrollment Period

11 months

First QC Date

November 18, 2024

Last Update Submit

November 18, 2024

Conditions

Falls with Injuries

Outcome Measures

Primary Outcomes (1)

  • Determine if the Fall TIPS initiative is effective at reducing falls at MRMC.

    Data will be collected from Verge and EPIC reports. To ensure intervention effectiveness, monitoring will be done through chart audits and staff reporting. EPIC slicer dicer generates customized reports, enhancing EHR effectiveness (Ayaad et al., 2022).

    through study completion, up to 18 months

Interventions

ObservationOTHER

Medical Records Chart Review

Eligibility Criteria

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

Patients with psychiatric conditions and cognitive impairments will be excluded from the project. This assessment is routine.

You may qualify if:

  • Adult (≥18 years) inpatients admitted for various medical-surgical conditions in 3 Medical unit at MRMC. All patients will be included in the project except those diagnosed with psychiatric conditions and cognitive impairments.

You may not qualify if:

  • Patients with psychiatric conditions and cognitive impairments will be excluded from the project. This assessment is routine.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Methodist Dallas Medical Center- Clinical Research Institute

Dallas, Texas, 75203, United States

RECRUITING

MeSH Terms

Interventions

Observation

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • ELIZABETH D AARON, MSN

    METHODIST RICHARDSON MEDICAL CENTER

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jeff Wilson, BS

CONTACT

2149471279JeffreyWilson@mhd.com

Colette Ngo Ndjom, MS

CONTACT

(214) 947-1289ColetteNgoNdjom@mhd.com

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 18, 2024

First Posted

November 20, 2024

Study Start

July 23, 2024

Primary Completion

July 1, 2025

Study Completion

July 1, 2025

Last Updated

November 20, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations

US(1)