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Physiotherapy in patients of abdominal surgery.

Effects of preoperative physiotherapy in cardiorespiratory conditions and physical functioning of patients undergoing upper abdominal surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-73vbv8
Enrollment
Unknown
Registered
2012-12-20
Start date
2010-10-27
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

Patients in the elective preoperative of: esophageous surgery, stomach surgery and billiar tract surgery.

Interventions

The patients will be allocated in the preoperative period to: intervention group (Arm 1) or control group (Arm 2). Arm 1: Patients are undergoing preoperative physiotherapy for 2 weeks (minimum) to 3
other
E02.779

Sponsors

Pontifícia Universidade Católica de Campinas
Lead Sponsor
Silvia Maria de Toledo Piza Soares
Collaborator

Eligibility

Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients with over 40 years of age. Scheduling of upper abdominal surgery elective (including surgery of esophagus, stomach or biliary tract surgery). Patients in preoperative elective period, at least 15 days and up to 21 days in advance of surgery. Physical and mental conditions that permit the evaluation of pulmonary function and walking test acceptable before surgery. Patients who signed an informed consent forms.

Exclusion criteria

Exclusion criteria: Patients with cerebrovascular or neuromuscular disease. Patients on immunosuppressive therapy before surgery. Prior pulmonary surgery history. Patients that had previously undergone surgery of the esophagus, stomach or biliary tract. Cardivascular instability. Patients undergoing physiotherapy in the eight weeks before inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Respiratory muscle strength as assessed using maximum inspiratory mouth pressure (MIP) and maximum expiratory mouth pressure (MEP). Values expressed in absolute (cmH2O) and % of predicted. Timepoint: Baseline (at inclusion in the study), 24 hours before surgery, within first 24 hours after surgery, seven days after surgery (or at discharge, if hospitalization time less than seven days after the operation) and thirty days after surgery.;Respiratory muscle endurance using inspiratory incremental effort test with linear loading device. Value expressed in absolute (cmH2O). Timepoint: Baseline (at inclusion in the study), 24 hours before surgery, within first 24 hours after surgery, seven days after surgery (or at discharge, if hospitalization time less than seven days after the operation) and thirty days after surgery.;Physical-functional performance evaluated with six minutes walk test. Distance walked expressed in absolute (meters) and % of predicted. Timepoint: Baseline (at inclusion in the study), 24 hours before surgery, seven days after surgery (or at discharge, if hospitalization time less than seven days after the operation) and thirty days after surgery.;Functional status as assessed using the functional independence measure (FIM). The score expressed: total dependece (18), modified dependence (19-60), modified independence (61-103) or total independence (104-126). Timepoint: Baseline (at inclusion in the study), 24 hours before surgery, within first 24 hours after surgery, seven days after surgery (or at discharge, if hospitalization time less than seven days after the operation) and thirty days after surgery.;Pulmonary function (spirometry) including vital capacity, forced vital capacity, forced expiratory volume in 1 second, expiratory forced flow peak . Measures expressed in absolute (liters or liters/second) and % of predicted. Timepoint: Baseline (at inclusion in the study), 24 hours before surgery, within first 24 hours after surgery, seven days after

Secondary

MeasureTime frame
Length of stay of patients in hospital according to medical records, expressed in days. Timepoint: Thirty days after surgery.

Countries

Brazil

Contacts

Public ContactSilvia Soares

Pontifícia Universidade Católica de Campinas

stpsoares@terra.com.br19-3343-6868

Outcome results

None listed

Source: REBEC (via WHO ICTRP)