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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04639349
Other study ID # P.T.REC/012/002897
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 19, 2020
Est. completion date March 1, 2021

Study information

Verified date November 2020
Source Cairo University
Contact Ali Ismail, lecturer
Phone 02 01005154209
Email allooka2012@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

exercise activity during the COVID pandemic is appreciated to be conducted in home especially for chronic chest diseases as chronic obstructive pulmonary disease (COPD) to reduce the chance of viral contamination during the COVID-19 pandemic.


Description:

40 COPD men will be divided to exercise group (20 patients) and control group (20 patients): the exercise group will receive a exercise session contains a fifty minutes exercise training at home with moderate intensity on the available training devices as bicycle or treadmill in addition to 30 minutes of exercising of upper and lower limb, the session will be repeated three times per week for eight weeks. The control group will not be trained


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date March 1, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers No
Gender Male
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria: - stable COPD patients - patients who will have a training device as bicycle or treadmill in home Exclusion Criteria: - diabetic patients - renal patients. - liver diseases

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
exercise group
the exercise group (20 patients) will receive a exercise session contains a fifty minutes exercise training at home with moderate intensity on the available training devices as bicycle or treadmill in addition to 30 minutes of exercising of upper and lower limb, the session will be repeated three times per week for eight weeks.
Other:
control group
the control group will not be trained

Locations

Country Name City State
Egypt Faculty of Physical Therapy Cairo University Giza Dokki

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary cortisol it will be measured in plasma It will be measured after eight weeks of training
Primary hospital anxiety and depression scale this a questionnaire that will assess anxiety and depression in COPD patients It will be measured after eight weeks of training
Secondary pulmonary function test it will be a measurement for lung volume and capacities It will be measured after eight weeks of training
Secondary Interleukin-8 It is an inflammatory marker in plasma It will be measured after eight weeks of training
Secondary body mass index it will measure body mass changes It will be measured after eight weeks of training
Secondary six minute walking test it assess functional capacity It will be measured after eight weeks of training
Secondary St. George's respiratory questionnaire It assess the effect of COPD on general quality of life It will be measured after eight weeks of training
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