- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04694768
Implementation of Rehabilitation Program for Post COVID-19
The Effect of Implementing a Nursing Program Intervention on Improvement of Health Quality of Post Covid-19 Patients
Many people who have suffered from the effects of this disease might now be at risk of long-term impairment and disability. The extent of this impairment and disability is yet unknown, but it is clear from early research that these patients will be in need of rehabilitation in all phases of the disease - acute, post-acute and long-term.
Rehabilitation is defined as "a set of interventions designed to reduce disability and optimize functioning in individuals with health conditions in interaction with their environment." Rehabilitation might very well be a key strategy to reduce the impact of COVID-19 on the health and function of people.
A team work is needed to implement this programs which are essential in all phases to facilitate early discharge, but even more to support and empower patients.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Assiut, Egypt, 71515
- Recruiting
- Aliae AR Mohamed-Hussein
-
Contact:
- Aliae A Mohamed-Hussein, MD
- Phone Number: 0122202352
- Email: aliaehussein@aun.edu.eg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Post acute COVID-19 patients
Exclusion Criteria:
- Acute COVID-10
- Non- COVID-19 patients
- Recent myocardial infarction
- Recent pulmonary embolism
- Neurologic diseases
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Optimizing health and functioning outcomes
Time Frame: 6 months
|
decrease intensive care acquired weakness
|
6 months
|
improve recovery and reduce disability
Time Frame: 6 months
|
decrease dyspnea, fatigue, anxiety and sleep disturbance
|
6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
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
- AssiutU19
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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