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NCT04694768 Clinical Trial

Implementation of Rehabilitation Program for Post COVID-19

Rehabilitation Clinical Trial

Official title:
The Effect of Implementing a Nursing Program Intervention on Improvement of Health Quality of Post Covid-19 Patients

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04694768
Other study ID # AssiutU19
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2020
Est. completion date January 31, 2021

Study information
Verified date January 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date January 31, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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 Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Rehabilitation
Rehabilitation program

Locations
Country Name City State
Egypt Aliae AR Mohamed-Hussein Assiut
Egypt Aliae AR Mohamed-Hussein Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Optimizing health and functioning outcomes decrease intensive care acquired weakness 6 months
Primary improve recovery and reduce disability decrease dyspnea, fatigue, anxiety and sleep disturbance 6 months
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