Rehabilitation Program for the Sequelae of COVID 19 Infection

Evaluate a Rehabilitation Program for the Sequelae of COVID 19 Infection: Description of a Clinical Practice

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04852718

Acronym

ISIS

Enrollment

120

Registered

2021-04-21

Start date

2021-04-13

Completion date

2021-04-13

Last updated

2021-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19

Brief summary

SUBPROJECT 1: Describe the situation of post-Covid patients in terms of muscle (skeletal and respiratory), cognitive, emotional and health-related quality of life in the 1st visit of the multidisciplinary post-covid rehabilitation consultation at the Hospital. Retrospective observational study. The data collected in clinical records during the first visit in the post-covid Rehabilitation consultation will be analysed. SUBPROJECT 2: Evaluate the response to a personalized rehabilitation program in patients with post-covid sequelae in terms of muscle (skeletal and respiratory), and health-related quality of life. Prospective observational study of a single cohort of patients. The data will be collected from successive clinical visits.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Inclusion criteria

* • Patients who were diagnosed with Covid-19 pneumonia, confirmed by serological tests or molecular biology test (PCR), and who were at home at the time of the 1st visit. * PCR or serological negative test or more than 28 days after diagnosis. * Dyspnoea in activities of daily living (mMRC ≥ 2), (Annex 5 of the clinical protocol). * Patients who had muscle weakness (Clinical Frailty Scale ≥ 3), (Annex 1 of the clinical protocol).

Exclusion criteria

* Patients with disease activity. * Live outside the reference area of the Hospital de la Santa Creu i Sant Pau. * Patients with cognitive impairment that makes it difficult to carry out the rehabilitation program.

Design outcomes

Primary

Measure	Time frame	Description
Muscular function	1 year	Short Physical Performance Battery (SPPB) value 0-12

Secondary

Measure	Time frame	Description
Health-related Quality of life	1 year	SF36 questionnaire, vaule 0-100
Respiratory muscle function	1 year	Maximal inspiratory pressure (MIP) Maximal expiratory pressure (MEP)
Exercise capacity	1 year	Six-minute walking Test (6MWT): meters,

Countries

Spain

Contacts

Primary ContactMaria-Rosa Güel-Rous, PhD

mguellr@santpau.cat34935565972

Outcome results