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Behavioural Intervention
NGAGE Tool for Family Engagement in Acute Cardiac Care (NGAGE Trial)
N/A
Recruiting
Research Sponsored by Lady Davis Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 48-hours of hospital discharge
Awards & highlights
NGAGE Trial Summary
This trial will test if a tool can improve family engagement in people hospitalized in an acute cardiac ward.
Who is the study for?
This trial is for adults over 18 who are family members of patients in acute cardiac care expected to stay longer than 48 hours. Participants must be able to communicate in English or French and willing to complete study questionnaires.Check my eligibility
What is being tested?
The NGAGE Trial tests a real-time feedback tool designed to improve family engagement during a loved one's hospitalization in an acute cardiac unit. Family members will either use the NGAGE tool or receive usual care, with outcomes measured at discharge.See study design
What are the potential side effects?
Since this trial involves using a feedback tool rather than medication, traditional side effects are not applicable. However, participants may experience emotional or psychological impacts from increased involvement in their loved one's care.
NGAGE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within 48-hours of hospital discharge
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 48-hours of hospital discharge
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Family Engagement (FAME) score
Secondary outcome measures
Family satisfaction
Mental health
NGAGE Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: NGAGE tool groupExperimental Treatment1 Intervention
Will have access to the NGAGE tool to learn about engaging in care and to request engagement activities.
Group II: Non-InterventionActive Control1 Intervention
Will receive usual care standards.
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Who is running the clinical trial?
Lady Davis InstituteLead Sponsor
44 Previous Clinical Trials
5,432 Total Patients Enrolled
2 Trials studying Family Engagement
270 Patients Enrolled for Family Engagement
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am willing to complete the study questionnaires.I cannot communicate in English or French.I am 18 years old or older.
Research Study Groups:
This trial has the following groups:- Group 1: Non-Intervention
- Group 2: NGAGE tool group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this research study still accepting participants?
"As per clinicaltrials.gov, the trial is currently open for enrollment and was originally published on April 1st 2023 with edits made as recently as July 2nd 2023."
Answered by AI
What is the aggregate number of individuals enrolled in this trial?
"Affirmative. Clinicaltrials.gov reveals that this clinical trial, which was initially published on April 1st 2023, is actively seeking participants. 88 individuals are required from a single site."
Answered by AI
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