BRacelet And Physical actiVity Evaluation (BRAVE)

Evaluation of Pre- and Post-operative Physical Activity on Postoperative Rehabilitation After Colorectal Surgery With a Connected Device

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02610790

Acronym

BRAVE

Enrollment

Registered

2015-11-20

Start date

2016-06-30

Completion date

2018-10-31

Last updated

2018-10-23

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

Conditions

Physical Activity

Keywords

connected bracelets, footsteps

Brief summary

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.

Detailed 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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame	Description
Pre- and postoperative physical activity	30 days	Number of footsteps

Secondary

Measure	Time frame	Description
Quality of life	30 days	score (number between 0 to 10)
Quality of sleep	30 days	Score (number between 0 to 10)
Pain	30 days	Score (number between 0 to 10)
Fatigue	30 days	Score (number between 0 to 10)

Countries

Switzerland

Outcome results