ESTUDIO DE APLICACIÓN DE ESCALAS PARA VALORACIÓN SINTOMÁTICA DEL SÍNDROME DE COVID PERSISTENTE
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- Fatigue
Study Overview
Brief Summary
The goal of this observational study is to learn about the long-term evolution of long COVID.
The main question it aims to answer is:
Does the main symptoms of the patients diagnosed with long COVID aproximate to those of patients who have had COVID acute infection without devoloping long COVID? Participants will answer mailed survey questions about their main symptons.
Detailed Description
Scales, indexes and questionnaires were mailed to 40 patients with long COVID to evaluate their main symptoms. Fatigue, emotional disorders, sleep disorders, cognitive impairments, dyspnea, physical activity, quality of life and pain were analyzed. The patients were reassessed after three years. The same scales, indexes and questionnaires were also sent to a control group of 40 volunteers of the same age and sex as the cases.
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 75 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •patients older than 18 years old and younger than 75 years old
- •patients who accepted to participate in the study
- •patients who have had COVID acute infection
- •patients who have long COVID (cases)
Exclusion Criteria
- •patients who refused to participate in the study at any time of the study
- •patients whose diagnosis of long COVID was revoked during the study (cases)
Outcomes
Primary Outcomes
Fatigue
Time Frame: From enrollment to three years later
MFIS scale
Emotional disorders
Time Frame: From enrollment to three years later
HADS scale
Sleep disorders
Time Frame: From enrollment to three years later
PSQI
Cognitive impairments
Time Frame: From enrollment to three years later
MFE-30
Dyspnea
Time Frame: From enrollment to three years later
mMRC
Physical activity
Time Frame: From enrollment to three years later
GPAQ
Quality of life (healthcare)
Time Frame: From enrollment to three years later
SF-36
Pain (healthcare)
Time Frame: From enrollment to three years later
EGDC
Secondary Outcomes
No secondary outcomes reported
Investigators
Andrés Carrascosa Gil
Médico Licenciado Especialista en Anestesiología y Reanimación
Hospital del Rio Hortega
