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Nursing Student for Work Injury

N/A
Recruiting
Led By Dre. Michelle Cardoso, PhD, Doctorate
Research Sponsored by University of New Brunswick
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre-intervention and post-intervention (within 2 weeks after intervention)
Awards & highlights

Study Summary

This trial aims to study a technology called Vendlet that helps with in-bed patient handling. The goal is to see if using Vendlet on a SAMS bed can reduce the physical strain on healthcare providers

Who is the study for?
This trial is for healthcare workers who haven't had pain or injury in their lower back or shoulders for at least a month. It's not open to those who've already been trained in proper patient handling techniques.Check my eligibility
What is being tested?
The study tests the Vendlet, a technology designed to help with moving patients in bed. It will be compared with standard patient handling on an adjustable SAMS bed, looking at how well it reduces physical strain on health care workers.See study design
What are the potential side effects?
Since this trial involves ergonomic training and use of a mechanical device rather than medication, traditional side effects are not applicable. However, participants may experience discomfort or muscle strain from using new equipment.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-intervention and post-intervention (within 2 weeks after intervention)
This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-intervention and post-intervention (within 2 weeks after intervention) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Bed Pressure Distribution: Average pressure distribution will be outcome measures to assess the safe placement of the patient.
Bed Pressure Distribution: Peak pressure distribution will be outcome measures to assess the safe placement of the patient.
Foot Pressure Distribution: Contact area will be the outcome measure of interest to assess postural balance and stability of the participant performing the patient handling technique.
+6 more
Secondary outcome measures
Exit Survey
Rating of Perceived Exertion (RPE)
Self Reported Questionnaires

Trial Design

1Treatment groups
Experimental Treatment
Group I: Nursing StudentExperimental Treatment1 Intervention
The study involves 1 single arm. A single group of participants will experience all experimental conditions. From an ergonomic standpoint, it has been recognized that providing patient-handling ergonomics training is crucial to their safety. This project will compare the same group performing patient handling tasks without training versus training while utilizing both long term care beds.

Find a Location

Who is running the clinical trial?

University of New BrunswickLead Sponsor
22 Previous Clinical Trials
2,528 Total Patients Enrolled
Dre. Michelle Cardoso, PhD, DoctoratePrincipal InvestigatorUniversite de Moncton
Dr. Wayne J Albert, PhD., DoctoratePrincipal InvestigatorUniversity of New Brunswick

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are patients currently eligible to enroll in this research study?

"Indeed, the information available on clinicaltrials.gov confirms that recruitment for this trial is ongoing. The trial was initially posted on September 20th, 2023 and last revised on February 27th, 2024. Enrollment targets are set at 30 participants from a single site."

Answered by AI

What is the current number of participants who are being recruited for this research study?

"Affirmative. Information on clinicaltrials.gov indicates that this trial is actively seeking participants. The study was initially listed on September 20, 2023 and most recently revised on February 27, 2024. They aim to recruit a total of 30 individuals from one designated site."

Answered by AI

Are individuals who are 85 years old and above eligible to participate in this study?

"Participants aged between 17 and 40 are eligible for this research project. There are separate studies available for individuals under 18 years old as well as those above 65."

Answered by AI

Is there a possibility for me to participate in this medical study?

"Individuals eligible for this study must have sustained a workplace injury and fall between the ages of 17 and 40. The trial has capacity for 30 participants in total."

Answered by AI
~19 spots leftby Apr 2025