usual care and follow-up by a nursePersonalized Multifactorial Intervention (IMP)
usual care and follow-up by a nurse: follow-up by a nurse and referral to a specialist(s) according to symptoms
Personalized Multifactorial Intervention (IMP): The content of the intervention is defined according to the result of the initial assessment in relation to the person's needs and the nature of his or her persistent symptoms. The patient, depending on his or her needs, may choose to participate in the following workshops :
* Knowledge of the disease and specific management, (led by the nurse)
* Covid-19 and anxiety/depression, (psychologist)
* Fatigue and adapted physical activities (video capsules)
* Covid-long and social link (professional and voluntary activities...) (social worker and/or nurse)
* The Recovery Café aims to provide a space for patients to listen to each other and share their experiences around themes related to the different dimensions of recovery: medical and psychological, economic, professional, social and existential.
Study summary
People with persistent symptoms of covid-19 have increased needs for needs for management of their overall health (physical, psychological and social). Persistent covid-19 symptoms have a negative impact on quality of life. By proposing a follow-up and an intervention on the reduction of these symptoms, the symptoms, the study will improve quality of life.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria
* Persons who have been infected with Covid-19.
* Person with persistent clinical signs of Covid-19 for more than 12 weeks, referred by one of the partner structures of the project. The persistent signs of Covid-19 are: fatigue which can be severe, neurological disorders neurological disorders (cognitive, sensory, headaches), cardio-thoracic disorders (pain and chest tightness, tachycardia, dyspnea, cough) and disorders of smell and taste. Pain, digestive disorders and skin disorders are also common.
* Person who has agreed to participate and has given informed consent to participate in the study
Exclusion Criteria:
* Refused to participate in the study
* Person under legal protection
* Person with severe cognitive impairment
Primary outcome measure(s)
the evolution of the quality of life — at the end of the 6-month follow-up measurement of quality of life at the end of the 6-month follow-up assess by the SF-36 questionnaire. This questionnaire has eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. Each question is evaluated on a Likert scale, with 3, 5 or 6 levels of possible answers. The 8 dimensions are also used to calculate two quality of life scores for individuals: the physical composite score (PCS) and the mental composite score (MCS). The higher the score, the greater the ability.
Trial sites (3)
Facility
City
Region
Status
Urps Medecins Libéraux Auvergne-Rhône-Alpes
Lyon
France
Chu Saint-Etienne
Saint-Etienne
France
DAC Loire
Saint-Etienne
France
More Centre Hospitalier Universitaire de Saint Etienne trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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