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

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

Study Locations

    • Guizhou
      • Zunyi, Guizhou, China, 563000
        • Recruiting
        • Zunyi Medical College
        • Contact:

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:

  1. Family members of trauma patients scheduled to be transferred from the EICU to a general unit within 24h;
  2. Family members of patients aged ≥ 18 years;
  3. Family members who are responsible for the main care tasks and medical decisions of the patient during hospitalisation;
  4. Family members of patients with clear language and good communication skills;
  5. Families of patients who volunteered to participate in this study.

Exclusion Criteria:

  1. Family members of patients temporarily transferred out of the EICU or temporarily discharged from trauma
  2. Families of patients who voluntarily request termination of treatment;
  3. 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.

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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