Post-COVID-19 Syndrome Clinical Trial
Official title:
Effect of Intensive Combined Rehabilitation Therapy for Patients With Post COVID 19 Chronic Fatigue Syndrome
The aim of this study is to investigate the effect of intensive combined rehabilitation therapy in form of Graded Exercise Therapy (GET) , Cognitive Behavioral Therapy (CBT) to treat patients with post COVID19 chronic fatigue syndrome .
Status | Not yet recruiting |
Enrollment | 60 |
Est. completion date | October 1, 2023 |
Est. primary completion date | September 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 34 Years |
Eligibility | Inclusion Criteria: - 60 post covid patients (6 months recovery after last negative PCR diagnosis) - Patients will be selected using the Oxford diagnostic criteria for CFS which required disabling fatigue to be the primary problem, in the absence of an exclusionary medical or psychiatric diagnosis. Patients will fulfil the following criteria for CFS : - fatigue as a principal symptom. - fatigue definite onset that is not life long. - fatigue should have been present for a minimum of 6 months during which it was present for more than 50% of the time. - Other symptoms may be present, particularly myalgia, mood and sleep disturbance. - Both sexs will be included - Body mass index range from (18.5 to 24.9 kg/m2) - Patients' age range will be 18 to 34 years old . - Presence of significant fatigue since COVID-19. - Able to understand and willing to sign a written informed consent document. - Willing and able to complete study procedures. Exclusion Criteria: - On medications that would influence exercise performance such as beta blockers or antiretroviral therapy - Enrolled in another interventional clinical research trial - Pregnancy - Significant hepatic or renal dysfunction - History or cardiac condition as determined by National Institutes of Health (NIH) cardiology to be unsafe for exercise participation (e.g. ischemic heart disease, right- or left-sided heart failure, cor pulmonale or pulmonary hypertension, dilated or hypertrophic cardiomyopathy or non-idiopathic cardiomyopathy) - Patients with a current diagnosis of schizophrenia, manic depressive illness, substance abuse, eating disorder or proven organic brain disease. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Cairo University |
Deale A, Chalder T, Marks I, Wessely S. Cognitive behavior therapy for chronic fatigue syndrome: a randomized controlled trial. Am J Psychiatry. 1997 Mar;154(3):408-14. — View Citation
Dennis A, Wamil M, Alberts J, Oben J, Cuthbertson DJ, Wootton D, Crooks M, Gabbay M, Brady M, Hishmeh L, Attree E, Heightman M, Banerjee R, Banerjee A; COVERSCAN study investigators. Multiorgan impairment in low-risk individuals with post-COVID-19 syndrome: a prospective, community-based study. BMJ Open. 2021 Mar 30;11(3):e048391. doi: 10.1136/bmjopen-2020-048391. — View Citation
Elboim-Gabyzon M, Buxbaum R, Klein R. The Effects of High-Intensity Interval Training (HIIT) on Fall Risk Factors in Healthy Older Adults: A Systematic Review. Int J Environ Res Public Health. 2021 Nov 11;18(22). pii: 11809. doi: 10.3390/ijerph182211809. Review. — View Citation
Greenhalgh T, Knight M, A'Court C, Buxton M, Husain L. Management of post-acute covid-19 in primary care. BMJ. 2020 Aug 11;370:m3026. doi: 10.1136/bmj.m3026. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The fatigue severity level | The fatigue severity level will be measured via the Arabic version of the Fatigue Severity Scale (FSS) | 12 weeks | |
Primary | aerobic capacity and endurance | Aerobic capacity and endurance will be measured via The 6 Minute Walk Test. The test will be performed at Modern University for the technology and information rehabilitation center corridor. | 12 weeks | |
Primary | Maximal hand grip strength and fatigue resistance | Maximal hand grip strength and fatigue resistance will be measured using the Handgrip dynamometer | 12 weeks | |
Primary | the Fall risk | Fall risk will measure via the Biodex Balance System (BBS) (Biodex Medical Systems Inc, Shirley, NY). | 12 weeks |
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