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Effect of GPR on rehabilitation and sleep after stroke

Effect of Global Posture Reeducation on rehabilitation and sleep after stroke

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
REBEC
Registry ID
RBR-9tvfk2
Enrollment
Unknown
Registered
2019-06-04
Start date
2019-03-20
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

Physiotherapy

Interventions

Physiotherapeutic rehabilitation through Global Posture Reeducation (RPG) can improve motor rehabilitation (functional mobility, ability in daily life activities) in post-stroke patients, and also ben
Other

Sponsors

Fundação de Amparo à Pesquisa do estado de São Paulo
Lead Sponsor
Universidade Federal de São Paulo
Collaborator
Fundação de Amparo à Pesquisa do estado de São Paulo
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients of both sexes, with age greater than or equal to 18 years of age; Patients with Apnea and Hypopnea Index ? 15; Patients with a history suggestive of a first acute stroke will be invited or may apply to participate in the study; Subacute stage of stroke (between 30 days and 3 months after disease onset); Magnetic Nuclear Resonance or Computed Tomography of the brain performed after hospital admission demonstrating ischemic or hemorrhagic stroke; Patients with NIHSS scores for stroke between 5 and 20 (moderate to moderate / severe stroke-motor impairment) at the time of entry study evaluation; Availability of attendance at physical therapy and assessment sessions; Accept in participating in the study and signing the Informed Consent Term (TCLE).

Exclusion criteria

Exclusion criteria: Patients with other associated neurological or sleep disorders that interfere with rehabilitation;Patients with renal insufficiency; Previous presence of stroke, subarachnoid hemorrhage or due to secondary cause, malformation, vasculitis, brain tumor or head trauma; Use of potent sedative drugs or continuous sedation; Patients with associated restrictive pulmonary or peripheral vascular diseases; Patients with congestive heart failure or class III or IV heart failure of the New York Heart Association Functional Classification; Non-cooperative patients due to lowering of level of consciousness, impairment of language, vision or important cognitive (verified by Montreal Cognitive Assessment (MoCA, Simões et al, 2008); Previous sleep breathing disorders under treatment; Patients who miss physical therapy sessions without replacement.

Design outcomes

Primary

MeasureTime frame
To measure the effect of physiotherapy on posture.;Avaliar o efeito da fisioterapia qualidade de sono por meio de questionários: Escala de sonolência de Epworth (corte = 9) e ÍOndice de qualidade de sono de Pitsburgh (10= indica disturbio de sono, antes e após 16 semanas de tratamento.;To evaluate the effect of physical therapy on the sleep pattern by means of an all-night polysomnography examination, according to the American Academy of Sleep Medicine criteria.

Secondary

MeasureTime frame
To evaluate the effect of sedestation / immobilism and standing / activity on the AHI and on the redistribution of fluids, measured by means of the Segmental Electric Bioimpedance Test.

Countries

Brazil

Contacts

Public ContactCristina Frange

Universidade Federal de São Paulo

cristina.frange15@gmail.com55 11 95443 2899

Outcome results

None listed

Source: REBEC (via WHO ICTRP)