A large proportion of persons who have had COVID-19 have reported persisted symptoms as fatigue and dyspnea months post infection which affect activities of daily living. The aim of the study is to examine the feasibility and safety of a concentrated rehabilitation program with a mobile application follow-up for persons with persistent symptoms post COVID-19 infection. We will examine recruitment availability, adherence to the program, goal achievement, and resources requirements. Methods: A feasibility study with one group pre-post test design with 10-20 persons between 18-67 years, with persistent symptoms post COVID-19 will be included. The intervention is 3+ 1-2 days concentrated rehabilitation with a mobile application follow-up for 3 months. Following assessments wil be used: Cardiopulmonary exercise testing, lung function, functional performance tests, questionnaires regarding dyspnea, fatigue, anxiety, depression, work-status, health status, sleep behavior, physical activity level. Demographic data before and after the intervention will be presented. Focus group interview will be done with the participants. The interview will be analysed using systematic text condensation.
In March 2020, the World Health Organization (WHO) declared the COVID-19 outbreak to be a pandemic, and a year later more than 120 000 000 people are confirmed with the disease. The disease has caused more than 2 700 000 deaths globally. Norway has a low mortality rate compared to rest of the world. However, a large proportion (10-33%) of the patients worldwide have reported persistent symptoms, such as dyspnea, reduced exercise capacity, loss of taste/smell and fatigue months after the infection. Persistent symptoms are also found in younger populations and in persons with an initially mild disease. The intervention will take place at "Helse i Hardanger" (HiH)(Health center in Hardanger, Norway). The participants will stay for a 3 -day rehabilitation intervention, if needed, another 1 or 2-day stay will be offered about a month later. The concentrated treatment will be given by an interdisciplinary team, including doctors, physiotherapists, nutritionists, pharmacists, psychologists/psychiatrists, and nurses. The intervention is an individualized group treatment based on behavioural change.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
3+ 1-2 days concentrated rehabilitation for patients with persistent symptoms post COVID-19 with a mobile application follow-up and physical consultations at 3 months post intervention.
Helse i Hardanger
Øystese, Kvam Herad, Norway
RECRUITINGCardiopulmonary exercise test (CPET)
CPET performed at treadmill
Time frame: 4 months
Chalder Fatigue Questionnaire (CFQ)
Assessing fatigue
Time frame: 4 months
International Physical Activity Questionnaire (IPAQ)
Assessing physical activity
Time frame: 4 months
Generalized Anxiety Disorder (GAD-7)
Evaluation of mental disorders
Time frame: 4 months
Patient Health Questionnaire (PHQ-9)
Assessing health status
Time frame: 4 months
Bergen Insomnia Scale (BIS)
Assessing sleep behavior
Time frame: 4 months
Client Satisfaction Questionnaire (CSQ-8)
Assessing client satisfaction with the treatment
Time frame: 3 months
Work and Social Adjustment Scale (WSAS)
Assessing ability to work and leisure activities.
Time frame: 4 months
The Brief Illness Perception Questionnaire (BIPQ)
Assessing the cognitive and emotional representations of illness.
Time frame: 4 months
Modified Medical Research Council Dyspnea Scale (mMRC)
Assessing dyspnea
Time frame: 4 months
Dyspnea-12
Assessing dyspnea
Time frame: 4 months
Stair Climbing Test (SCT)
Evaluation of functional exercise capacity
Time frame: 4 months
30 second sit to stand test (30STST)
Evaluation of functional exercise capacity
Time frame: 4 months
Spirometry, plethysmography and maximal voluntary ventilation
Evaluation of lung function
Time frame: 4 months
Bioimpedance measurement
Assessment of body composition
Time frame: 4 months
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