COVID-19 Respiratory Infection, Parkinson Disease
Conditions
Keywords
pain, chest mobility, cough, muscle strength, physical activity, quality of life
Brief summary
To comparative pain intensity, chest mobility, cough strength, muscle strength, physical activity levels and quality of life in Parkinson's patients with post-COVID-19 and without post-COVID-19 was aimed in current study. Knowledge in the literature regarding this topic is still obscure.
Detailed description
Acute worsening and long-term sequelae of motor and non-motor symptoms have also been described in Parkinson's patients during and after SARS-CoV-2 infection, which is also known as prolonged COVID. The effects of COVID-19 on pain, chest mobility, cough strength, muscle strength, physical activity levels and quality of life in Parkinson's patients are still unclear today. For this reason, in this study, it was aimed to comparatively investigate pain, chest mobility, cough strength, muscle strength, physical activity levels and quality of life in Parkinson's patients with COVID-19 and without COVID-19 and to show the relationships between these outcome measures.
Interventions
In this research, the data of Parkinson's patients who have had COVID-19 will be collected face to face. Chest mobility, cough strength, muscle strength, physical activity and quality of life will be evaluated in all Parkinson's patients. The data to be obtained through all these evaluations will be collected from at one time and in a time lasting maximum of about 1 hour. Step count tracking with pedometer will be done for 3 days for each individual.
In this research, the data of Parkinson's patients who have not had COVID-19 will be collected face to face. Chest mobility, cough strength, muscle strength, physical activity and quality of life will be evaluated in all Parkinson's patients. The data to be obtained through all these evaluations will be collected from at one time and in a time lasting maximum of about 1 hour. Step count tracking with pedometer will be done for 3 days for each individual.
Sponsors
Izmir Democracy University
Study design
Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
for Parkinson's patients with post-COVID-19; * Being diagnosed with COVID-19 at least 12 weeks ago and recovered, * Being over 18 years old, * Volunteering to participate in the research, * Being diagnosed with Parkinson's disease * Comorbid conditions (such as hypertension, diabetes) are under control * Being able to perceive assessments (Standardized Mini Mental Test score of 24 and above) * Having the ability to ambulate and walk independently * Being in stage 1 - 4 according to the Modified Hoehn-Yahr Scale Inclusion criteria for Parkinson's patients without post-COVID-19; * Not being diagnosed or suspected of COVID-19 * Being over 18 years old, * Volunteering to participate in the research, * Being diagnosed with Parkinson's disease * Having comorbid conditions (such as hypertension, diabetes) which are under control * Being able to perceive assessments (Standardized Mini Mental Test score of 24 and above) * Having the ability to ambulate and walk independently * Being in stage 1 - 4 according to the Modified Hoehn-Yahr Scale
Exclusion criteria
for Parkinson's patients with and without post-COVID-19; * Sudden drug or dose change during the study period * A history of any acute/chronic orthopedic, cardiovascular, pulmonary, psychiatric or neuromuscular disease that may prevent measurements from being made. * Having had myocardial infarction and pulmonary embolism in the last 30 days, * Having a history of additional neurological (stroke, head trauma, peripheral nerve diseases, brain and spinal cord tumors, etc.) diseases other than Parkinson's disease * Having severe vision loss or vestibular dysfunction * Patients with blood pressure values above 140/90 and below 90/50 in blood pressure measurements made before the study, with arrhythmia on ECG, with a history of shortness of breath and/or palpitation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Total quality of life score evaluated by Parkinson's Disease Questionnaire (PDQ-39) questionnaire. | through study completion, an average of 1 year | The status of quality of life will be evaluated using Parkinson's Disease Questionnaire (PDQ-39) questionnaire. Parkinson's Disease Questionnaire-39 (PDQ39) is a 39-item quality of life questionnaire. Evaluation for each question item ranges from 0 (no problem) to 4 (constant problem). Low scores in total indicate an improvement in people's quality of life. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Cough Strength | through study completion, an average of 1 year | Cough Strength will be evaluated using a Peak Flow Meter. |
| Daily average step count | through study completion, an average of 1 year | Daily average step counts will be recorded via a pedometer everyday within 3 days after confirming enrolment. All individuals will be asked to carry their pedometers with them during the day and record to their diaries. |
| Hand grip strength | through study completion, an average of 1 year | Hand grip strength will be evaluated using a hand dynamometer. |
| Chest mobility | through study completion, an average of 1 year | Chest mobility will be evaluated using a tape measure. |
| Cognitive status | through study completion, an average of 1 year | Cognitive state will be evaluated using The mini-mental state examination (MMSE). It is an 11 question test. The highest score from the test is 30 points. Scores of 23 and lower indicate cognitive dysfunction, and scores of 24 and higher indicate normal cognitive level. |
Countries
Turkey (Türkiye)
Outcome results
None listed