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Comparison between conventional physical therapy and Pilates' Method in the evolution of functionality, respiratory muscle strength and exercise capacity in hospitalized chronic renal patients

Effectiveness of conventional physical therapy and Pilates' method in functionality, respiratory muscle strength and ability to exercise in hospitalized chronic renal patients: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-96jrm5
Enrollment
Unknown
Registered
2013-09-01
Start date
2013-01-09
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

Chronic Kidney Failure

Interventions

The control group (conventional physiotherapy): 28 patients receive physiotherapy session corresponding to passive exercises, active or active-assisted resisted with shoulder abduction, elbow flexion,
walking on the front, side and back and legs raising associating arms marching, evolving into eyes closed. Experimental group: 28 patients are undergoing 10 Pilates sessions, once a day, every day, wi
balance
joint stabilization, pelvic, trunk and spine
body awareness
axial lengthening and strengthening the abdominal muscles, upper and lower limbs for a program that has been developedbased on theoretical and practical information. The exercises were adapted by a te
Other
H02.010.625
E02.779.483.750
E02.190.525.186
N02.278.354.422.615
E02.779

Sponsors

UNIVERSIDADE CIDADE DE SÃO PAULO
Lead Sponsor
Hospital do Rim e Hipertensão
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: No acute neuropathy or lung disease, or also rheumatic and orthopedic diseases associated that prevent them from performing the proposed protocol; those who have cognitive ability to respond to the questionnaire and ability to ambulate.

Exclusion criteria

Exclusion criteria: Will be excluded immediate postoperative abdominal surgery, from the upper or lower abdomen; those who present, at the time of hospitalization, the need for use of noninvasive mechanical ventilation and intubation; those who present thrombocytopenic; those with diagnosis of deep vein thrombosis and who require intensive medical support

Design outcomes

Primary

MeasureTime frame
Functionality: Assessed by the Barthel Index at the moments of pre intervention, fifth session, tenth session and / or hospital discharge, and three months after randomization.;Exercise Capacity: Assessed by the Modified Incremental Step Test at the moments of pre-intervention, fifth session, tenth session and / or discharge;Respiratory Muscle Strength: Assessed by Manovacuometry at the moments of pre-intervention, fifth session, tenth session and / or discharge—

Secondary

MeasureTime frame
Patient Satisfaction: Assessed by MedRisk questionnaire at the moment of discharge;Length of stay: evaluate the mean number of days of hospitalization in each group and compare them with each other—

Countries

Brazil

Contacts

Public ContactLuciana Chiavegato

UNIVERSIDADE CIDADE DE SÃO PAULO

lu_chiavegato@uol.com.br11-2178-1565

Outcome results

None listed

Source: REBEC (via WHO ICTRP)