Vitamin D Deficiency Clinical Trial
Official title:
Effect of Aerobic Interval Training Combined With Vitamin D Supplement on Functional Capacity and Perceived Myalgia in Middle Aged Obese Women
NCT number | NCT04319289 |
Other study ID # | 2020HAAE |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 12, 2020 |
Est. completion date | May 20, 2020 |
Verified date | May 2020 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aimed to investigate whether there will be an effect of adding a program of aerobic interval training in managing patients suffering from myalgia associated with vitamin D deficiency.
Status | Completed |
Enrollment | 45 |
Est. completion date | May 20, 2020 |
Est. primary completion date | May 15, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 30 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Forty five sedentry women with non specific myalgia pain. - The patients' ages ranged from 30 -40 years. - All patients have non specific muscle pain for more than 2 months. - They have vitamin D deficiency. - All patients have BMI from 25 to 34.9 kg/m2. - All patients were clinically and medically stable when attending the study. Exclusion Criteria: - Unstable cardiovascular and chest problems. - Patients with diseases which affect vitamin D level as a history of rheumatic or metabolic bone diseases and diabetes. - Patients taking drugs which affect vitamin D level as steroids and anticonvulsants drugs . - Musculoskeletal disorders which may affect their physical ability to do the exercises. |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Physical Therapy | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Concentration of Plasma Serum vitamin D level (25OHD) | It is performed by Laboratory BioPlex® 2200 System | It is performed before and after the study(12 weeks interval) for all groups | |
Primary | Description of Functional capacity efficiency | Cooper 12-Minute Walk Test (12MWT) | It is performed before and after the study(12 weeks interval) for all groups | |
Primary | Intensity of non specific muscle pain (myalgia) | A 10-cm Visual Analogue Scale (VAS) was used to evaluate the patients' pain , with 0 representing no pain and 10 representing the worst pain imaginable | It is performed before and after the study(12 weeks interval) for all groups | |
Primary | Description of the improvement in Quality of life | The Short form health survey (SF-12)is often used to compare health status between groups of patients, to indentify predictors of health status | It is performed before and after the study(12 weeks interval) for all groups |
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