- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05834387
The Impact of a Transitional Care Management Programme on the Migration Stress of Family Members of Patients
July 9, 2023 updated by: Xu Ren, Zunyi Medical College
The Impact of a Transitional Care Management Programme on the Migration Stress of Family Members of Patients Transferred Out of the EICU Under the "Health Care-family-environment" Linkage Model
This study investigated the impact of the establishment and application of the "health care-family-environment" linkage mechanism on the level of migration stress, coping styles and care satisfaction of families of patients transferred from the EICU, in order to provide a reference for improving the physical and psychological health of families and to promote the role of family members in the social support of patients transferred out of this category.
Study Overview
Status
Recruiting
Conditions
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xu Ren
- Phone Number: 18311639591
- Email: r19921115x@qq.com
Study Locations
-
-
Guizhou
-
Zunyi, Guizhou, China, 563000
- Recruiting
- Zunyi Medical College
-
Contact:
- Xu Ren
- Phone Number: 18311639591
- Email: r19921115x@qq.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Family members of trauma patients scheduled to be transferred from the EICU to a general unit within 24h;
- Family members of patients aged ≥ 18 years;
- Family members who are responsible for the main care tasks and medical decisions of the patient during hospitalisation;
- Family members of patients with clear language and good communication skills;
- Families of patients who volunteered to participate in this study.
Exclusion Criteria:
- Family members of patients temporarily transferred out of the EICU or temporarily discharged from trauma
- Families of patients who voluntarily request termination of treatment;
- Family members of patients with cognitive impairment, speech impairment or mental abnormalities.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
|
Nursing interventions in the experimental group The interventions were based on the "health care-family-environment" linkage
|
|
Experimental: Control group
|
EICU Transfer Routine Care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress assessment
Time Frame: 48 hours
|
Stress assessment assessed by ICU Transfer Stress Assessment Scale for Families of Patients Transferring Out
|
48 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Xu Ren, Zunyi Medical College
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2023
Primary Completion (Estimated)
November 1, 2023
Study Completion (Estimated)
May 1, 2024
Study Registration Dates
First Submitted
April 11, 2023
First Submitted That Met QC Criteria
April 25, 2023
First Posted (Actual)
April 28, 2023
Study Record Updates
Last Update Posted (Actual)
July 11, 2023
Last Update Submitted That Met QC Criteria
July 9, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Zunyi001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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