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BRacelet And Physical actiVity Evaluation (BRAVE)

L

Lausanne University Hospital (CHUV)

Status

Completed

Conditions

Physical Activity

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to quantify pre- and postoperative physical activity of patients operated on colorectal surgery. Daily physical activity (No. of footsteps) is going to be recorded from 15 days before surgery to the end of hospitalization after surgery in a prospective cohort of consecutive colorectal patients by use of an attached strap. Then, the investigators will propose physical activity thresholds (adapted to the age, gender and patient comorbidities) to optimize the ERAS protocol (Enhanced Rehabilitation After Surgery). Thus, this analysis will allow the investigators to provide patients with physical rehabilitation programs "a la carte" during a hospitalization for colorectal surgery. Connected bracelets will directly involve patients in their care and rehabilitation.

Full description

Connected bracelet will be given to 50 consecutive patients undergone colorectal surgery 15 days before surgery. The investigators will measure pre- and postoperative physical activity. It is an observational activity of patient's physical activity during the perioperative period with no intervention.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with a colorectal surgery

Exclusion criteria

  1. Limitation of linguistic or cognitive abilities, interfering with the understanding of the study protocol
  2. Lack of consent of the study form
  3. Emergency Surgery
  4. stoma closure

Trial design

50 participants in 1 patient group

Connected bracelet
Description:
Patients with a colorectal surgery planned will be included. Fifteen days before surgery, patients will have a connected bracelet permitting to quantify the number of steps and distance achieved each day before surgery.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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