- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06175585
Construction of Theoretical Model of Medical Treatment Behavior of Patients With Chronic Kidney Disease
Construction of a Theoretical Model of Medical Behavior of Patients With Chronic Kidney Disease From the Perspective of Supply: An Empirical Analysis Based on Andersen Behavior Model
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Jie Zheng, Associate professor
- Phone Number: +8618636667799
- Email: zhengjie@sxmu.edu.cn
Study Locations
-
-
Shanxi
-
Taiyuan, Shanxi, China, 030001
- Recruiting
- The Second Hospital of Shanxi Medical University
-
Contact:
- Zheng Jie, Associate professor
- Phone Number: +8618636667799
- Email: zhengjie@sxmu.edu.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria:
- Patients diagnosed with ESRD and treated with dialysis for more than 3 months;
- Patients aged ≥18 years old;
- Patients with complete clinical data;
- Patients who are clearly conscious and can accurately express their willingness;
- Patients who have signed informed consent and are willing to cooperate with the study.
Exclusion criteria:
- Patients with other serious systemic diseases, such as severe cardiovascular and cerebrovascular diseases, severe diabetes, etc.;
- Patients with mental disorder, such as cognitive or intellectual disability;
- Patients with a history of anxiety and depression;
- Patients with intermittent loss of consciousness or are unable to understand the questions in the questionnaire.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
traditional nursing group
|
Patients undergoing MHD received traditional nursing interventions, encompassing various aspects such as dietary advice, instructions on medication usage, health education, emphasis on precautions during dialysis, and guidelines for vascular access care.
Additionally, the nurses proactively inquired about patients' emotional well-being during the nursing shift change, actively engaged and uplifted patients experiencing low spirits, and encouraged family members to provide emotional support.
|
narrative nursing group
|
The narrative nursing process is based on the practice of "two-line system" proposed by Jiang, which is carried out in a separate classroom, office or ward with sufficient space and good lighting. The environment is set to the right temperature and humidity for comfortable face-to-face conversation. This process is done in stages, depending on how often the patient is dialysis three or more times a week. Each session lasts about 30 minutes and the whole process lasts four weeks. Adjust to the specific needs of each patient . |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Zung's Self-Rating Anxiety Scale
Time Frame: one week
|
assess the anxiety and depression levels of patients
|
one week
|
Self-rating Depression Scale
Time Frame: one week
|
assess the anxiety and depression levels of patients
|
one week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019041044-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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