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Digital Multimodal Rehabilitation for People With Post-acute COVID-19 Syndrome. (REHABCOVID)

Primary Purpose

Post-COVID Syndrome

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
RehabCovid_Telematic
RehabCovid_ImmersiveVR
Control_Condition
Sponsored by
Consorci Sanitari de Terrassa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-COVID Syndrome focused on measuring COVID-19, Immersive Virtual Reality, Cognition, Cognitive Training, Physical Exercise, Mindfulness

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Over 18 years old. Participants with a diagnosis of COVID-19 presenting persistent neurological symptoms at least 12 weeks after acute infection. They will have objective cognitive impairment (1.5 SD below estimated premorbid IQ on one or more neuropsychological tests) Consent from a physician to engage in an exercise intervention Exclusion Criteria: Established diagnosis before COVID-19 disease of psychiatric, neurological, developmental disorder, or systemic pathologies are known to cause cognitive deficits. Motor or sensory alterations that impede the rehabilitation program.

Sites / Locations

  • Consorci Sanitari de TerrassaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Telematic group

Immersive Virtual Reality group

Active control program

Arm Description

This program combines cognitive training, physical exercise, and mindfulness tasks delivered remotely to participants. The cognitive training includes 24 interactive sessions over 12 weeks aimed at training attention, memory, and executive function. The physical exercise program is personalized and includes balance work, stretching, and muscle strengthening exercises, with two sessions per week for 12 weeks. The mindfulness component adapts the Mindfulness-Based Stress Reduction program, including body scanning, seated meditation, and gentle Hatha yoga, with one supervised session per week via video call over 12 weeks. The program is designed for autonomous use by participants.

The sessions will consist of carrying out a face-to-face multimodal stimulation program with the application of MK360 immersive technology for the cognitive, emotional, behavioral, physical, functional - social areas. The multimodal intervention includes 24 interactive sessions two sessions per week, over 12 weeks. They will follow the following scheme: Welcome and awareness of the here and now. Physical activation. Cognitive stimulation. Relaxation techniques and Mindfulness. Feedback and end of session. During the intervention period, patients will be provided with a downloadable App with a username and password, so they can access it. From the App, they will view the tests to answer according to tempos and therapeutic direction.

In paper or pdf format, patients in the active control group will receive guidelines for physical and cognitive stimulation to do autonomously at home. Patients in the active control group will receive guidelines for cognitive and physical stimulation and meditation exercises in paper or pdf format, to be done independently at home. They will be encouraged to do physical exercises, meditation, and cognitive activities two times a week.

Outcomes

Primary Outcome Measures

Differences between groups in scores of global cognition
Global cognition was assessed with the Montreal Cognitive Assessment (MoCA) a screening tool designed to identify mild cognitive impairment (MCI) and other cognitive deficits. The MoCA takes around 10-15 minutes to complete and consists of 30 items (range=0-30). Higher scores mean a better outcome.
Differences between groups in scores of selective attention, inhibition, and processing speed
Selective attention, inhibition, and processing speed are measured with the Stroop Color and Word Test. Participants are asked to name the color of a series of color patches (Stroop Color Naming), read a series of color words (Stroop Word Reading), and name the color of a series of color words where the word and color do not match (e.g., the word "red" written in blue ink), Stroop Color-Word Interference. Higher scores mean a better outcome.
Differences between groups in scores of Visual scanning and processing speed
Visual scanning and processing speed are measured with the Trail-Making Test-A version. Participants are asked to connect a series of numbered circles on a page in numerical order. Higher scores mean a better outcome.
Differences between groups in scores of Executive functioning and cognitive flexibility
Executive functioning and cognitive flexibility are measured with the Trail-Making Test-B version. Participants are asked to connect a series of circles that contain both numbers and letters in alternating numerical and alphabetical order. Higher scores mean a better outcome.
Differences between groups in scores of auditory attention
Auditory attention is measured with Digit Span Forward from WAIS-IV. Participants are asked to repeat numbers in the same order as read aloud by the examiner. Higher scores mean a better outcome.
Differences between groups in scores of working memory_DSB
Working memory is measured with Digit Span Backward from WAIS-IV. Participants are asked to repeat the numbers in the reverse order of that presented by the examiner. Higher scores mean a better outcome.
Differences between groups in scores of Perceptual Reasoning
Perceptual Reasoning is measured with Matrices from the WAIS-IV. Participants are presented with a pattern or design with one missing piece and are asked to select the correct piece from a set of options to complete the pattern. Higher scores on the Perceptual Reasoning Index mean a better outcome.
Differences between groups in scores of sustained attention and impulsivity
Conners Continuous Performance Test - 2nd edition (CPT-II) is task-oriented computerised assessment of attention-related problems. Participants are presented with a repetitive array of visual stimuli on a computer screen for 14 min. Participants are instructed to press the space bar every time a letter other than "X" appears and to not press the space bar when "X" appears. The rate of stimulus presentation varies according to 1, 2, and 4 s intervals throughout the task. Measures: Correct Detection (Higher rates indicate better outcome), Reaction times (Lower scores indicate better outcome), Omission errors (Lower rates indicate better outcome), and Commission errors (Lower rates indicate better outcome).
Differences between groups in scores of processing speed
The Digit Symbol Coding subtest from the WAIS-III is a neuropsychological assessment instrument for the detection of brain dysfunction in children and adults. It consists of replacing symbols that lack verbal meaning with numbers based on a key. Higher scores indicate better outcomes.
Differences between groups in scores of verbal memory and learning
Verbal memory and learning are measured with the Rey Auditory Verbal Learning Test (RAVLT). It is a word-learning test where five presentations of a 15-word list are given, each followed by an attempted recall. This is followed by a second 15-word interference list (list B), followed by a recall of list A. Delayed recall and recognition are also tested. Higher scores mean a better outcome.
Differences between groups in scores of phonetic fluency
Phonetic fluency is measured with the FAS test. It consists of saying words that start with a certain letter, as many words as possible must be mentioned during a specific time of 1 minute. The standard administration of the test provides three letters, the most used are the letters F, A, and S. Higher scores indicate better performance.
Differences between groups in scores of semantic verbal fluency
Semantic verbal fluency is measured with the ANIMAL test. It consists of generating the name of as many species of animals as possible within 1min. Higher scores indicate better performance.
Differences between groups in scores of memory and everyday forgetfulness
Memory and everyday forgetfulness are measured with The Memory Failures of Everyday-MFE Questionnaire is a self-reported test that allows an assessment of memory and everyday forgetfulness. It is a unifactorial questionnaire and consists of 30 items. The total score results from the sum of the scores in each item, from 1 to 30. The MFE can assess the current situation of the patients and their evolution long-term or changes due to treatment. Scores <8 represent an optimal memory function. Lower scores indicate better outcomes.

Secondary Outcome Measures

Differences between groups in scores of anxiety
Anxiety is measured with the 7-item Generalized Anxiety Disorder Scale (GAD-7), a Likert-type scale with questions ranging from "not at all" (0 points) to "nearly every day" (3 points). The maximum score is 24. Higher scores mean a worse outcome.
Differences between groups in scores of depression
Depression is measured with the Patient Health Questionnaire-9 (PHQ-9) which scores each of the 9 DSM-IV criteria as "not at all" (0 points) to "nearly every day" (3 points). Higher scores mean a worse outcome.
Differences between groups in scores of Mindfulness levels
Mindfulness levels are measured with The Mindful Attention Awareness Scale (MAAS) assesses an individual's level of mindfulness, including attention, awareness, and non-judgment. The 15-item self-report questionnaire uses a 6-point Likert scale to measure an individual's general tendency to be aware of and attentive to their current experience. Scores on the MAAS range from 15 to 90, with higher scores indicating greater levels of mindfulness. A higher score suggests better outcome.
Differences between groups in scores of Fatigue
Fatigue is measured with the Chalder Fatigue Scale, an 11-item questionnaire measuring the severity of physical and mental fatigue on two separate subscales. Seven items represent physical fatigue (items 1-7) and 4 represent mental fatigue (items 8-11). Each item " less than usual" (0) to " much more than usual" (3). The ratings of items are added together to calculate the total score (range=0-33). High scores represent high levels of fatigue.
Differences between groups in scores of psychological flexibility
Psychological flexibility is measured with the Acceptance and Action Questionnaire, a 7-point Likert scale, ranging from 1 ("never true") to 7 ("always true"), indicating how frequently they experience the described behavior or feeling in their daily lives. The scale has 9 items and the total score ranges from 9 to 63, with higher scores indicating greater levels of psychological flexibility (better outcome).
Differences between groups in Functionality
Functionality is measured with a 12-item World Health Organization Disability Assessment Schedule-II (WHODAS-II). Patients are asked to state the level of difficulty experienced, considering how they usually do the activity. The scale scores each item as "none" (1) to "cannot do" (5). The total score is calculated with an SPSS syntax, and the range varies from 0 to 100, with higher scores reflecting more significant disability.
Differences between groups in scores of Sleep Quality
Sleep Quality is measured with The Pittsburgh Sleep Quality Index (PSQI). This test presents 24 items, although only 19 are taken into account for the correction. This test is divided into 7 dimensions, namely, sleep quality, sleep onset latency, sleep duration, sleep efficiency, sleep disturbances, hypnotic drugs, and daytime dysfunction. Higher scores indicate worse sleep quality.
Differences between groups in scores of Quality of Life
Quality of Life is measured with EuroQol a self-completion questionnaire, which consists of five questions: covering mobility, hygiene, activities, pain, and anxiety. The descriptive system divides each of the 5 dimensions into three levels of response: the absence of a problem, some problem, and extreme problem. Lower scores indicate better outcomes. In addition, the questionnaire has a plus scale where the participants rated their health state on a scale of 0-100. In this scale, higher scores indicate better outcome.
Differences between groups in scores of performed physical activity
Performed physical activity is measured with The International Physical Activity Questionnaire (IPAQ) is a questionnaire composed of 7 questionsin order to assessthe frequency, duration, and intensity (vigorous or moderate) of the performed physical activity, walking, and sitting time during a business day for the last 7 days. Later, from the minutes obtained from the participant's answers, the METS (metabolic equivalent tasks) conversion is performed, allowing a classification, depending on the energy consumption obtained for each activity, into three categories (low, medium, high). Higher score indicate better outcome.
Differences between groups in White Matter integrity
White matter integrity: tractography measured by MRI
Differences between groups in brain Volumetry
Grey and white matter volume measured by MRI
Differences between groups in Resting-state connectivity
Resting state brain activity using fMRI
Differences between groups in plasmatic Interleukin- 6 (IL-6)
The plasma levels of IL-6 are measured with enzyme-linked immunosorbent assay (ELISA) Kit
Differences between groups in plasmatic Nerve Growth Factor (NGF)
The plasma levels of NGF are measured with ELISA Kit
Differences between groups in plasmatic Glial Fibrillary Acidic Protein (GFAp) and neurofilament light chain- NFL
The plasma levels of GFAp are measured with ELISA Kit
Differences between groups in plasmatic lipid peroxidation products
The plasma levels of malondialdehyde are measured with TBARS assay method
Differences between groups in plasmatic Ferritin
The plasma levels of Ferritin are measured with biochemical assay
Differences between groups in plasmatic C-Reactive Protein (CRP)
The plasma levels of CRP are measured with high sensitivity c-reactive protein ELISA Kit
Differences between groups in rate of expression analysis of Sirt-1 levels
Sirt-1 levels are measured with the Sirtuin-1 ELISA Kit
Differences between groups in rate of expression analysis of different microRNAs
microRNAs are measured with TaqMan miRNA qRT-PCR

Full Information

First Posted
May 4, 2023
Last Updated
May 5, 2023
Sponsor
Consorci Sanitari de Terrassa
Collaborators
University of Barcelona, Universitat de Girona, Unitat Assistencial i Preventiva de l'Esport- Centre d'Alt rendiment, Politecnic University of Catalonia, Corporación Fisiogestión
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1. Study Identification

Unique Protocol Identification Number
NCT05846126
Brief Title
Digital Multimodal Rehabilitation for People With Post-acute COVID-19 Syndrome.
Acronym
REHABCOVID
Official Title
Digital Rehabilitation With Cognitive Training, Physical Activity and Mindfulness for People With Post-acute COVID-19 Syndrome With Cognitive Impairment. REHABCOVID Project.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2023 (Actual)
Primary Completion Date
September 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Consorci Sanitari de Terrassa
Collaborators
University of Barcelona, Universitat de Girona, Unitat Assistencial i Preventiva de l'Esport- Centre d'Alt rendiment, Politecnic University of Catalonia, Corporación Fisiogestión

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Although most infected people survive the infection, many have persistent sequelae or symptoms, which cause disability or decreased quality of life. The World Health Organization has called on countries to prioritize the rehabilitation of the consequences of COVID-19 in both the medium and long term, as this chronicity is expected to impact the health public and the economy in the coming years. RehabCOVID (also referred to as RehabNautilus) is born from the need to provide solutions to persistent cognitive impairment symptoms of people who have suffered from COVID-19. Thus, we will offer people with long COVID that accomplish inclusion/exclusion criteria to participate in a randomized clinical trial to evaluate the effectiveness of cognitive stimulation therapy combined with physical exercise and mindfulness. The current project is a single-blind randomized control study, where we will compare two combined interventions with a control group that will encompass different functional, structural, and biochemical changes and interactions in the brain. We will study the effects that this combined intervention produces in the brain. We expect to gain more insight into the specific neuroplasticity mechanisms of cognitive persistent COVID symptoms.
Detailed Description
The current project is a single-blind randomized clinical study, where we will compare two combined interventions with a control group that will encompass different functional, structural, and biochemical changes and interactions in the brain. We will study the effects that this combined intervention produces in the brain. We expect to gain more insight into the specific neuroplasticity mechanisms of cognitive persistent COVID symptoms. Specifically, we aim to: Examine the effects of a combined intervention in a population of long-COVID patients on various domains: cognition; emotion; physical health and quality of life. Study the molecular mechanisms (biomarkers of inflammation, vascular risk, growth factors, angiogenesis, neurogenesis, and cellular metabolism markers of neural plasticity) by which the combined interventions influence brain functions. Compare the levels of neural plasticity-related miRNAs and Sirt-1 protein in the plasma of long-COVID patients of the experimental groups versus the active control group. Examine specific plasticity effects of each of the two interventions regarding structural magnetic resonance imaging (MRI) combined with volumetry and morphometry, resting-state functional MRI. Determine the influence that demographic characteristics, previous pathologies, lifestyle, baseline brain state, and genetic polymorphisms can have on neuroplasticity. We hypothesize that we will find recovery in our three groups, although it will be enhanced in the two experimental groups (those that combine cognitive training with physical activity and mindfulness) compared to our control group. Post-COVID patients of the experimental groups will perform better than those patients of the active control group in cognition (episodic memory tests, executive function, attention, and speed processing), functional capacity, mental health, and quality of life measures at the end of the intervention. Post-COVID patients of the experimental groups will show greater changes in biomarkers than those patients of the active control group at the end of the intervention. These changes will include higher levels of Sirt-1 and regulation of neural plasticity-related miRNAs in plasma from patients in the experimental group. We will find an association between changes in biomarkers and cognitive, functional capacity and mental health outcomes in individuals of the experimental groups. Post-COVID patients of the experimental groups will show greater improvements in grey and white matter structural data and functional connectivity than those patients of the active control group at the end of the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-COVID Syndrome
Keywords
COVID-19, Immersive Virtual Reality, Cognition, Cognitive Training, Physical Exercise, Mindfulness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
158 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Telematic group
Arm Type
Experimental
Arm Description
This program combines cognitive training, physical exercise, and mindfulness tasks delivered remotely to participants. The cognitive training includes 24 interactive sessions over 12 weeks aimed at training attention, memory, and executive function. The physical exercise program is personalized and includes balance work, stretching, and muscle strengthening exercises, with two sessions per week for 12 weeks. The mindfulness component adapts the Mindfulness-Based Stress Reduction program, including body scanning, seated meditation, and gentle Hatha yoga, with one supervised session per week via video call over 12 weeks. The program is designed for autonomous use by participants.
Arm Title
Immersive Virtual Reality group
Arm Type
Experimental
Arm Description
The sessions will consist of carrying out a face-to-face multimodal stimulation program with the application of MK360 immersive technology for the cognitive, emotional, behavioral, physical, functional - social areas. The multimodal intervention includes 24 interactive sessions two sessions per week, over 12 weeks. They will follow the following scheme: Welcome and awareness of the here and now. Physical activation. Cognitive stimulation. Relaxation techniques and Mindfulness. Feedback and end of session. During the intervention period, patients will be provided with a downloadable App with a username and password, so they can access it. From the App, they will view the tests to answer according to tempos and therapeutic direction.
Arm Title
Active control program
Arm Type
Active Comparator
Arm Description
In paper or pdf format, patients in the active control group will receive guidelines for physical and cognitive stimulation to do autonomously at home. Patients in the active control group will receive guidelines for cognitive and physical stimulation and meditation exercises in paper or pdf format, to be done independently at home. They will be encouraged to do physical exercises, meditation, and cognitive activities two times a week.
Intervention Type
Behavioral
Intervention Name(s)
RehabCovid_Telematic
Intervention Description
A multimodal and digitally-based cognitive training, physical exercise, and mindfulness intervention delivered remotely.
Intervention Type
Behavioral
Intervention Name(s)
RehabCovid_ImmersiveVR
Intervention Description
A multimodal and digitally-based cognitive training, physical exercise and mindfulness intervention delivered face to face and through 360MK Virtual Reality technology
Intervention Type
Behavioral
Intervention Name(s)
Control_Condition
Intervention Description
Traditional paper or pdf format multimodal intervention that will combine cognitive, mediation and physical activities.
Primary Outcome Measure Information:
Title
Differences between groups in scores of global cognition
Description
Global cognition was assessed with the Montreal Cognitive Assessment (MoCA) a screening tool designed to identify mild cognitive impairment (MCI) and other cognitive deficits. The MoCA takes around 10-15 minutes to complete and consists of 30 items (range=0-30). Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of selective attention, inhibition, and processing speed
Description
Selective attention, inhibition, and processing speed are measured with the Stroop Color and Word Test. Participants are asked to name the color of a series of color patches (Stroop Color Naming), read a series of color words (Stroop Word Reading), and name the color of a series of color words where the word and color do not match (e.g., the word "red" written in blue ink), Stroop Color-Word Interference. Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Visual scanning and processing speed
Description
Visual scanning and processing speed are measured with the Trail-Making Test-A version. Participants are asked to connect a series of numbered circles on a page in numerical order. Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Executive functioning and cognitive flexibility
Description
Executive functioning and cognitive flexibility are measured with the Trail-Making Test-B version. Participants are asked to connect a series of circles that contain both numbers and letters in alternating numerical and alphabetical order. Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of auditory attention
Description
Auditory attention is measured with Digit Span Forward from WAIS-IV. Participants are asked to repeat numbers in the same order as read aloud by the examiner. Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of working memory_DSB
Description
Working memory is measured with Digit Span Backward from WAIS-IV. Participants are asked to repeat the numbers in the reverse order of that presented by the examiner. Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Perceptual Reasoning
Description
Perceptual Reasoning is measured with Matrices from the WAIS-IV. Participants are presented with a pattern or design with one missing piece and are asked to select the correct piece from a set of options to complete the pattern. Higher scores on the Perceptual Reasoning Index mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of sustained attention and impulsivity
Description
Conners Continuous Performance Test - 2nd edition (CPT-II) is task-oriented computerised assessment of attention-related problems. Participants are presented with a repetitive array of visual stimuli on a computer screen for 14 min. Participants are instructed to press the space bar every time a letter other than "X" appears and to not press the space bar when "X" appears. The rate of stimulus presentation varies according to 1, 2, and 4 s intervals throughout the task. Measures: Correct Detection (Higher rates indicate better outcome), Reaction times (Lower scores indicate better outcome), Omission errors (Lower rates indicate better outcome), and Commission errors (Lower rates indicate better outcome).
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of processing speed
Description
The Digit Symbol Coding subtest from the WAIS-III is a neuropsychological assessment instrument for the detection of brain dysfunction in children and adults. It consists of replacing symbols that lack verbal meaning with numbers based on a key. Higher scores indicate better outcomes.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of verbal memory and learning
Description
Verbal memory and learning are measured with the Rey Auditory Verbal Learning Test (RAVLT). It is a word-learning test where five presentations of a 15-word list are given, each followed by an attempted recall. This is followed by a second 15-word interference list (list B), followed by a recall of list A. Delayed recall and recognition are also tested. Higher scores mean a better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of phonetic fluency
Description
Phonetic fluency is measured with the FAS test. It consists of saying words that start with a certain letter, as many words as possible must be mentioned during a specific time of 1 minute. The standard administration of the test provides three letters, the most used are the letters F, A, and S. Higher scores indicate better performance.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of semantic verbal fluency
Description
Semantic verbal fluency is measured with the ANIMAL test. It consists of generating the name of as many species of animals as possible within 1min. Higher scores indicate better performance.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of memory and everyday forgetfulness
Description
Memory and everyday forgetfulness are measured with The Memory Failures of Everyday-MFE Questionnaire is a self-reported test that allows an assessment of memory and everyday forgetfulness. It is a unifactorial questionnaire and consists of 30 items. The total score results from the sum of the scores in each item, from 1 to 30. The MFE can assess the current situation of the patients and their evolution long-term or changes due to treatment. Scores <8 represent an optimal memory function. Lower scores indicate better outcomes.
Time Frame
Before the intervention and 12 weeks later
Secondary Outcome Measure Information:
Title
Differences between groups in scores of anxiety
Description
Anxiety is measured with the 7-item Generalized Anxiety Disorder Scale (GAD-7), a Likert-type scale with questions ranging from "not at all" (0 points) to "nearly every day" (3 points). The maximum score is 24. Higher scores mean a worse outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of depression
Description
Depression is measured with the Patient Health Questionnaire-9 (PHQ-9) which scores each of the 9 DSM-IV criteria as "not at all" (0 points) to "nearly every day" (3 points). Higher scores mean a worse outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Mindfulness levels
Description
Mindfulness levels are measured with The Mindful Attention Awareness Scale (MAAS) assesses an individual's level of mindfulness, including attention, awareness, and non-judgment. The 15-item self-report questionnaire uses a 6-point Likert scale to measure an individual's general tendency to be aware of and attentive to their current experience. Scores on the MAAS range from 15 to 90, with higher scores indicating greater levels of mindfulness. A higher score suggests better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Fatigue
Description
Fatigue is measured with the Chalder Fatigue Scale, an 11-item questionnaire measuring the severity of physical and mental fatigue on two separate subscales. Seven items represent physical fatigue (items 1-7) and 4 represent mental fatigue (items 8-11). Each item " less than usual" (0) to " much more than usual" (3). The ratings of items are added together to calculate the total score (range=0-33). High scores represent high levels of fatigue.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of psychological flexibility
Description
Psychological flexibility is measured with the Acceptance and Action Questionnaire, a 7-point Likert scale, ranging from 1 ("never true") to 7 ("always true"), indicating how frequently they experience the described behavior or feeling in their daily lives. The scale has 9 items and the total score ranges from 9 to 63, with higher scores indicating greater levels of psychological flexibility (better outcome).
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in Functionality
Description
Functionality is measured with a 12-item World Health Organization Disability Assessment Schedule-II (WHODAS-II). Patients are asked to state the level of difficulty experienced, considering how they usually do the activity. The scale scores each item as "none" (1) to "cannot do" (5). The total score is calculated with an SPSS syntax, and the range varies from 0 to 100, with higher scores reflecting more significant disability.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Sleep Quality
Description
Sleep Quality is measured with The Pittsburgh Sleep Quality Index (PSQI). This test presents 24 items, although only 19 are taken into account for the correction. This test is divided into 7 dimensions, namely, sleep quality, sleep onset latency, sleep duration, sleep efficiency, sleep disturbances, hypnotic drugs, and daytime dysfunction. Higher scores indicate worse sleep quality.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of Quality of Life
Description
Quality of Life is measured with EuroQol a self-completion questionnaire, which consists of five questions: covering mobility, hygiene, activities, pain, and anxiety. The descriptive system divides each of the 5 dimensions into three levels of response: the absence of a problem, some problem, and extreme problem. Lower scores indicate better outcomes. In addition, the questionnaire has a plus scale where the participants rated their health state on a scale of 0-100. In this scale, higher scores indicate better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in scores of performed physical activity
Description
Performed physical activity is measured with The International Physical Activity Questionnaire (IPAQ) is a questionnaire composed of 7 questionsin order to assessthe frequency, duration, and intensity (vigorous or moderate) of the performed physical activity, walking, and sitting time during a business day for the last 7 days. Later, from the minutes obtained from the participant's answers, the METS (metabolic equivalent tasks) conversion is performed, allowing a classification, depending on the energy consumption obtained for each activity, into three categories (low, medium, high). Higher score indicate better outcome.
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in White Matter integrity
Description
White matter integrity: tractography measured by MRI
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in brain Volumetry
Description
Grey and white matter volume measured by MRI
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in Resting-state connectivity
Description
Resting state brain activity using fMRI
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in plasmatic Interleukin- 6 (IL-6)
Description
The plasma levels of IL-6 are measured with enzyme-linked immunosorbent assay (ELISA) Kit
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in plasmatic Nerve Growth Factor (NGF)
Description
The plasma levels of NGF are measured with ELISA Kit
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in plasmatic Glial Fibrillary Acidic Protein (GFAp) and neurofilament light chain- NFL
Description
The plasma levels of GFAp are measured with ELISA Kit
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in plasmatic lipid peroxidation products
Description
The plasma levels of malondialdehyde are measured with TBARS assay method
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in plasmatic Ferritin
Description
The plasma levels of Ferritin are measured with biochemical assay
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in plasmatic C-Reactive Protein (CRP)
Description
The plasma levels of CRP are measured with high sensitivity c-reactive protein ELISA Kit
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in rate of expression analysis of Sirt-1 levels
Description
Sirt-1 levels are measured with the Sirtuin-1 ELISA Kit
Time Frame
Before the intervention and 12 weeks later
Title
Differences between groups in rate of expression analysis of different microRNAs
Description
microRNAs are measured with TaqMan miRNA qRT-PCR
Time Frame
Before the intervention and 12 weeks later

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Over 18 years old. Participants with a diagnosis of COVID-19 presenting persistent neurological symptoms at least 12 weeks after acute infection. They will have objective cognitive impairment (1.5 SD below estimated premorbid IQ on one or more neuropsychological tests) Consent from a physician to engage in an exercise intervention Exclusion Criteria: Established diagnosis before COVID-19 disease of psychiatric, neurological, developmental disorder, or systemic pathologies are known to cause cognitive deficits. Motor or sensory alterations that impede the rehabilitation program.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maite Garolera
Phone
+34937310007
Email
mgarolera@cst.cat
Facility Information:
Facility Name
Consorci Sanitari de Terrassa
City
Terrassa
ZIP/Postal Code
08227
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maite Garolera
Phone
+34937310007
Email
mgarolera@cst.cat

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Digital Multimodal Rehabilitation for People With Post-acute COVID-19 Syndrome.

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