Physiotherapy for Persistent COVID-19 Disease Using Aerobic Exercise

Universidad Francisco de Vitoria

Status: Completed

Conditions: COVID-19; Genetic Predisposition to Disease

Treatments: Genetic: Control; Device: Experimental

Study type: Interventional

Funder types: Other

Identifiers

NCT05453188

URJCLactate

Details and patient eligibility

About

Aerobic exercise - Nordic walking in Persistent Covid (PC) vs. healthy controls.

The main objective of this study is to analyse the genes associated with increased physical performance in patients with PC vs. healthy controls and to measure the level of lactic acid in blood, pre and post exercise session in patients affected by PC.

Relevance: It is intended to be a tool for patients with CP who have not been hospitalised, nor have been offered outpatient rehabilitation treatment. They have not recovered their work, family, sporting or leisure functions. They have particular problems in returning to aerobic exercise.

We think that they may need to be accompanied in the recovery of their physical condition under the supervision of health professionals. Most of the studies offered to them are exploratory, not intervention. Our proposal is a 12-week intervention.

Our proposal, delves into the mechanisms that may underlie their fatigue and their problems in returning to aerobic exercise, in order to collaborate in approaching possible solutions.

Secondary objectives: To study in each of the patients with persistent covid, included in the aerobic Nordic walking programme, their DNA in order to, based on two candidate genes, analyse the role of genetic polymorphisms associated with increased VO2 max training, compared to a healthy control group.

To assess the blood lactic acid level pre and post exercise in a group of patients with persistent covid pre and post aerobic Nordic walking programme. Patients and Methods: 33 patients with CP and 33 healthy controls will follow a Nordic walking programme for 12 weeks. QIAGEN Cube automatic extractor and lactic acid meter will be used.

Full description

Design: Parallel non-randomized clinical trial. Study arms: Experimental group with Nordic walking programme (n=15) and healthy control group with the same programme (n=15).

Patients will be recruited by means of a mass mailing to their addresses in the Covid Persistente Madrid group. Participants must meet the inclusion criteria and sign the informed consent form. Patients will be asked to submit a recent basic blood test and an electrocardiogram if available.

Medical Rehabilitation Consultation for screening of patients It is assumed that the patient has already been diagnosed with longCOVID, so he/she should provide data from previous clinical history in relation to the process: time of evolution, characteristics of the syndrome, and treatments carried out.....

It is essential that the patient provides a recent blood test. Objectives To ascertain the main symptomatology presented by the patient, with relevance of signs and symptoms that cause functional limitation.

Determine the presence of comorbidities that may be a contraindication or precaution for the practice of the activity.

The estimated effect size for the main outcome measures established in this project was 0.25. Considering a power of the statistical test of 0.95, an alpha error of 0.05 and a total of five measurements in two participant groups, a minimum number of 30 participants is required, according to the G*Power software (version 3.1.7). Taking into account a loss rate of 10%, the sample size will finally consist of 30 subjects (15 subjects for each intervention group). In order to prevent possible losses, 17 subjects will be included in each group.

5.3. Spatial scope

The assessment will take place:

Consultations with the rehabilitation doctor will take place at the University Clinic of the Faculty of Health Sciences of the Rey Juan Carlos University, Madrid, Spain.

Genetic analysis: Faculty of Health Sciences. Francisco de Vitoria University. Lactic acid measurement: Outdoors, pre- and post-Nordic walking session. Since the measurement must be immediate.

The intervention will take place in the outdoor space of the Casa de Campo. Madrid, Spain.

The Nordic walking sessions will last 90 minutes (warm-up, exercise and cool down), and will be carried out for 12 weeks, with a frequency of once a week.

The instructor will start by designing routes without gradients during the first four sessions of intervention and will adapt the protocol for the following two months according to the evolution of the groups and adapted to the needs of the longCOVID patients.

Patients will be asked to record post-exercise fatigue and their heart rate and oxygen saturation will be monitored during the sessions.

DNA collection for the determination of polymorphisms will be performed on samples to optimize resources (samples will be anonymized and coded).

Samples will be obtained by swabbing and scraping of the buccal mucosa by the participant. DNA will be isolated by QIAGEN Cube automatic extractor. The DNA will be stored at -20º until use.

The genetic study will analyze single nucleotide polymorphisms (SNPs) related fundamentally to functions associated with:

• Polymorphisms of genes associated with muscle performance; ACE, ACTN3, AMPD1, CKM and MLCK
• Polymorphisms of genes for sensitivity and resistance to Covid-19 infection; ACE-2 The data will be entered into the SPSS statistical package (version 25) for analysis.

First, the Kolmogorov-Smirnov test will be used to determine whether the study variables show a normal distribution (p>0.05). Those quantitative variables that do not show a normal distribution will be analysed with non-parametric tests and their data will be expressed as median and interquartile range, while quantitative variables that show a normal distribution will be analysed with parametric tests and their data expressed as mean and standard deviation.

For variables with a normal distribution, a repeated measures analysis of variance (ANOVA) with Bonferroni a posteriori adjustment will be performed, establishing as an inter-subject factor the group parameter (experimental and control) and as an intra-subject factor each of the measurements.

The contrast of variables that do not follow a normal distribution will be carried out using the Mann-Whitney U test, comparing the differences between the groups in each measurement. Intra-group differences will be analysed using the Friedman test for k related samples. In case this test detects intra-group differences at follow-up, the Wilcoxon signed-rank test for two related samples will be used.

Between-group analysis of qualitative variables, expressed as proportions and percentages, will be performed using Pearson's chi-squared test. Intra-group differences of qualitative variables will be performed using McNemar's test for paired data.

The statistical analysis will be carried out with a confidence level of 95%, so that values with a p-value of less than 0.05 will be considered significant.

Enrollment: 30 patients

Sex: All

Ages: 30 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Persistent symptoms of covid for more than one year.
• Age between 30 and 60 years.
• Complete vaccination schedule (one dose is sufficient, as this was considered by the Ministry for patients who have passed the disease).
• Recent basic blood test.

Exclusion criteria

• Presence of comorbidities of musculoskeletal origin that contraindicate the practice of the proposed exercise.
• Presence of uncontrolled cardiac or respiratory disease.
• Presence of incapacitating neurological disease that significantly interferes with the proposed exercise activity Severe anaemia or other co-morbidities that significantly interfere with the proposed exercise activity
• Diagnosis or symptoms of dysautonomia
• Presence of high rates of fatigue
• Desaturations during the exercise test that imply a need for oxygen supply for exercise
• Desaturation on exertion during exercise ≥3%.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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30 participants in 2 patient groups

LongCOVID

Experimental group

Description:

Patients who have had COVID-19 and have been diagnosed with longCOVID or persistent COVID

Treatment:

Device: Experimental

Genetic: Control

Control

Active Comparator group

Description:

Patients who have had COVID-19, but have not been diagnosed with longCOVID or persistent COVID

Treatment:

Device: Experimental

Genetic: Control