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Symptom-based Rehabilitation Compared to Usual Care in Post-COVID - a Randomized Controlled Trial

Not Applicable
Completed
Conditions
Long-COVID
COVID-19
Interventions
Other: symptom-focused rehabilitation
Other: usual care
Registration Number
NCT05172206
Lead Sponsor
Schön Klinik Berchtesgadener Land
Brief Summary

Inpatient, multimodal rehabilitation represents one of the most important interventions in the disease management of post/long COVID. Different professional societies, including the German Society of Pneumology and the European Respiratory Society, recommend rehabilitation intervention to reduce the sequelae of COVID-19. However, from the perspective of science and practice, there are relevant areas that have been insufficiently investigated and are essential for the treatment success of post/long COVID patients:

* Differentiation of rehabilitation effects from natural recovery after COVID-19.

* Lack of personalized and symptom-based treatment approaches that can address the heterogeneity of symptoms in post/long COVID

* Lack of uniform, high-quality rehabilitation standards in post-/long-COVID.

Therefore, post-COVID patients will be recruited at several post-COVID practices around Germany and randomized to receive (A) a rehabilitation program or (B) usual care. The primary objective of this randomized controlled trial (RCT) is to investigate whether a 3-week symptom-oriented, inpatient, multidisciplinary rehabilitation intervention, whose content focus is standardized according to cluster assignment (fatigue, cognition, soma), has a positive effect on the quality of life (primary outcome) in post-COVID syndrome patients compared to a usual care group (standard outpatient care). All study participants will be provided with a continuous telemonitoring system (SaniQ app) throughout the study period. After the interventional phase, there will be a 3 months follow-up assessment to evaluate the maintenance effects of COVID rehabilitation.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
132
Inclusion Criteria
  • Post-COVID Syndrome according to World Health Organisation definition (persistent symptoms for at least 3 months after PCR-test confirmed SARS-CoV 2 infection)
Exclusion Criteria
  • no walking ability
  • not able to operate smartphone apps
  • rehabilitation program within the previous 6 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Symptom-focused Rehabilitationsymptom-focused rehabilitationPatients in this arm will be referred to a 3-week inpatient comprehensive rehabilitation program. Initially, patients will be classified into one out of three clusters namely: Cluster A (Fatigue), Cluster B (cognition), or Cluster C (physical). The content of the rehabilitation program will be individually adapted according to the patient's most relevant symptom cluster.
Usual Careusual carePatients in this arm do not receive any intervention beyond usual care during the study phase. However, all patients in this group will get the opportunity to also receive a rehabilitation program after the study phase.
Primary Outcome Measures
NameTimeMethod
Change from baseline Quality of life assessed by Short Form - 12 Questionnaire at week 4 and week 12baseline, week 4, week 12

the scale of the physical and mental Health component summary score ranges from minimum 0 to maximum 100 points with higher scores indicating better quality of life

Secondary Outcome Measures
NameTimeMethod
Change from baseline COVID-related symptoms at week 4 and week 12baseline, week 4, week 12

the number of COVID-symptoms will recorded as well as their intensity will be rated on a scale from 0 \[not relevant\] until 10 \[very severe symptom\].

Change from baseline lung function at week 4 and week 12baseline, week 4, week 12

following Parameters will be collected: forced expiratory volume in 1 sec, peak flow, forced vital capacity, total lung capacity, diffusion lung capacity for carbonmonoxide

Change from baseline blood gas analysis at week 4 and week 12baseline, week 4, week 12

following parameters will be collected at rest and at the end of an incremental cycle test: partial pressure for oxygen and carbon dioxide

Change from baseline Cardiac Doppler echocardiography at week 4 and week 12baseline, week 4, week 12

Left and right heart echocardiography will be performed

Change from baseline laboratory parameters at week 4 and week 12baseline, week 4, week 12

blood samples will be taken from venous blood

Change from baseline exercise performance at week 4 and week 12baseline, week 4, week 12

incremental cardiopulmonary exercise testing will be performed with spirometry

Change from baseline health care service needs at week 4 and week 12baseline, week 4, week 12

Number of visits at the general practitioner, pulmonologist, psychologist, physiotherapist, COVID-ambulance, hospital admission until the last visit will be recorded

Change from baseline working capability at week 4 and week 12baseline, week 4, week 12

number of days of incapacity to work until the last visit will be recorded

Change from baseline sleep quality at week 4 and week 12baseline, week 4, week 12

daytime sleepiness will be assessed by using the Epworth Sleepiness Scale (total score ranges from 0 to 24 with higher scores indicating higher impairment)

Change from baseline Depression status assessed by Patient Health Questionnaire 9baseline, week 4, week 12

the total score ranges from 0 to 27 points with higher scores indicating worse Depression symptoms

Change from baseline Anxiety status assessed by Generalized Anxiety Disorder Scale 7baseline, week 4, week 12

the total score ranges from 0 to 21 points with higher scores indicating more anxiety symptoms

Change from baseline resilience assessed by resilience scale 13baseline, week 4, week 12

the total score ranges from 13 to 91 points with higher scores indicating higher resilience

Change from baseline cognitive status assessed by Montreal Cognitive Assessment Testbaseline, week 4, week 12

the total score ranges from 0 to 30 points with higher scores indicating a better cognitive status

Change from baseline dyspnea assessed by Modified Medical Research Counsil score at week 4 and week 12baseline, week 4, week 12

the total score ranges from 0 to 4 points with higher scores indicating more dyspnea

Change from baseline dysfunctional breathing assessed by Nijmegen breathing questionnaire at week 4 and week 12baseline, week 4, week 12

the total score ranges from 0 to 64 points with higher scores indicating hyperventilation

Change from baseline chronic fatigue syndrome assessed by fatigue assessment scale at week 4 and week 12baseline, week 4, week 12

the total score ranges from 10 to 50 points with higher scores indicating more fatigue

Change from baseline chronic fatigue syndrome assessed by canadian consensus criteria at week 12baseline, week 12

the canadian consensus criteria indicate if patients developed a chronic fatigue syndrome/myalgic encephalomyelitis

Change from baseline functional status assessed by post-COVID functional status scale at week 4 and week 12baseline, week 4, week 12

the total score ranges from 0 to 4 points with higher scores indicating more impairment

Change from baseline physical activity assessed by Garmin watch at week 4 and week 12baseline, week 4, week 12

daily total steps per day will be recorded by a Garmin watch linked to the SaniQ App

Change from baseline blood pressure assessed at week 4 and week 12baseline, week 4, week 12

blood pressure will be measured at the upper arm using the Aponorm device

Change from baseline oxygen saturation assessed by pulse oximeter at week 4 and week 12baseline, week 4, week 12

Beurer pulse oximeter

Change from baseline peak flow assessed by peak flow meter at week 4 and week 12baseline, week 4, week 12

peak flow will be assessed by smart one spirometer

Trial Locations

Locations (8)

University Hospital Augsburg

🇩🇪

Augsburg, Germany

Praxis Dr. Schrag

🇩🇪

Bad Reichenhall, Germany

Pneumopraxis Marburg

🇩🇪

Marburg, Germany

Pneumologen Lichterfelde Berlin

🇩🇪

Berlin, Germany

Praxis im Zentrum Erlangen

🇩🇪

Erlangen, Germany

Lungenärzte am Rundfunkplatz, München

🇩🇪

Munich, Germany

COVID ambulance Prof. Koczulla

🇩🇪

Schönau am Königssee, Germany

Praxis Dr. Roch

🇩🇪

Schwabach, Germany

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