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Behavioural Intervention
Nurse-Led Care Coordination for Multi-Morbidity
N/A
Waitlist Available
Led By Binu Koirala, PhD
Research Sponsored by Johns Hopkins University
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 baseline, 6 weeks, and after completion of intervention up to 3 months
Awards & highlights
Study Summary
This trial aims to reduce symptom burden & improve quality of life for people with multiple chronic conditions. A nurse-led intervention w/ telephone support is proposed.
Who is the study for?
This trial is for English-speaking patients at Johns Hopkins Hospital's IMCU who are about to be discharged and have two or more chronic conditions. It's not open to those unable to consent or with cognitive impairments.Check my eligibility
What is being tested?
The CO-ORDINATE program, a nurse-led intervention combined with telephone support aimed at improving care coordination and symptom management for people living with multiple chronic illnesses.See study design
What are the potential side effects?
Since this is a non-medical intervention focusing on care coordination and symptom management, traditional side effects associated with medications are not applicable.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 6 weeks, and after completion of intervention up to 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6 weeks, and after completion of intervention up to 3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Quality of Life assessed by Short Form Survey (SF-36) score
Change in Symptom burden assessed by Edmonton Symptom Assessment System (ESAS) score
Secondary outcome measures
Change in Health-care utilization
Trial Design
1Treatment groups
Experimental Treatment
Group I: InterventionExperimental Treatment1 Intervention
A patient-centered Care cO-ORDInatioN And sympTom managEment (CO-ORDINATE) intervention
Find a Location
Who is running the clinical trial?
Johns Hopkins UniversityLead Sponsor
2,266 Previous Clinical Trials
14,837,472 Total Patients Enrolled
National Institute of Nursing Research (NINR)NIH
580 Previous Clinical Trials
10,376,536 Total Patients Enrolled
Binu Koirala, PhDPrincipal InvestigatorJohns Hopkins School of Nursing
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am able to understand and consent to participate in the trial.
Research Study Groups:
This trial has the following groups:- Group 1: Intervention
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.
Are there still opportunities for recruitment into this research endeavor?
"Evidenced on clinicaltrials.gov, this research venture is presently enrolling participants and has done so since November 22nd 2022 with the latest update occurring August 2nd 2023."
Answered by AI
How many participants are engaged in this clinical investigation?
"Affirmative. Clinicaltrials.gov affirms that this clinical trial, which was initially introduced on November 22nd 2022, is presently enrolling patients - 25 to be exact from a single site."
Answered by AI
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