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Respiratory Treatment Protocol after Covid-19

Respiratory Muscle Intervention Protocol in Subjects After Covid-19 Infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5xp96cq
Enrollment
Unknown
Registered
2021-09-28
Start date
2021-10-15
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Dyspnea

Interventions

Thirty post-Covid-19 participants will be studied, randomized into two groups: inspiratory muscle training group (GTMI) and control group (CG). The initial assessment will include, in addition to the
lung function
respiratory muscle assessment, upper and lower limb strength
balance, and functional capacity. For both groups, an outpatient rehabilitation session will consist of aerobic and strength training, respiratory muscle training, bronchial hygiene maneuvers (when ne
and new PImax measurements will be performed every six sessions (two weeks) for load adjustment.
E02.190.525.186

Sponsors

Universidade Metodista de Piracicaba
Lead Sponsor
Universidade Metodista de Piracicaba
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Volunteers after COVID-19; no physical therapy treatment after hospital discharge; both sexes; hospitalized for 15 days or more; with respiratory and motor sequelae; able to carry out the proposed assessments and training

Exclusion criteria

Exclusion criteria: Volunteers with no hospitalization history; decompensated heart diseases; musculoskeletal and/or neuromuscular changes; with three consecutive absences in treatment

Design outcomes

Primary

MeasureTime frame
Evaluate the effects of an inspiratory muscle training (IMT) protocol on lung function, assessed through spirometry; respiratory muscle strength, assessed through manovacuometry; peripheral muscle strength, assessed using a dynamometer; physical fitness assessed through the six-minute step test (TD6) and autonomic modulation of heart rate, assessed by a frequency meter. A variation of at least 10% is expected in pre- and post-intervention measurements.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactTamires Mori
tamires.mori@live.com+55-019-996815092

Outcome results

None listed

Source: REBEC (via WHO ICTRP)