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Functional Performance Following Emergency High-risk Abdominal Surgery

Completed
Conditions
Emergency High-risk Abdominal Surgery
Interventions
Other: Evaluation of functional performance
Registration Number
NCT02124356
Lead Sponsor
Hvidovre University Hospital
Brief Summary

Emergency abdominal surgery is associated with high mortality rates, multiple postoperative complications and prolonged duration of hospital admission. The purpose of this study is to examine the postoperative functional performance in patients undergoing Emergency High-risk Abdominal Surgery. The hypothesis is that the study can describe the patient population in relation to postoperative functioning, degree of inactivity and the factors that limit mobility.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Patients (19 years and older) undergoing emergency laparotomy or laparoscopy (inclusive reoperations after elective surgery).
Exclusion Criteria
  • Patients undergoing minor emergency operations (uncomplicated appendectomy, laparoscopic cholecystectomy, diagnostic laparoscopy or laparotomy without intervention)

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Emergency High-risk Abdominal SurgeryEvaluation of functional performance-
Primary Outcome Measures
NameTimeMethod
Basic mobility evaluated by the Cumulated Ambulation Score (CAS)Daily on postoperative day 1 to 7 and at discharge from the hospital (average length of stay is: 14 days).

Factors that limit independency in basic mobility will be evaluated on a daily basis.

Secondary Outcome Measures
NameTimeMethod
Assessment of Motor and Process Skills (AMPS)One time at postoperative day 4.

AMPS measures a person's performance capacity for activities of daily living (ADL) and/or independent living.

Physical activity assessment with accelerometer (ActivePAL)Daily on postoperative day 1 to 7.
Visual Analog Scale (VAS)Daily on postoperative day 1 to 7 and at discharge from the hospital (average length of stay is: 14 days).

VAS is a self-reported measure of pain intensity.

Trial Locations

Locations (1)

Hvidovre University Hospital

🇩🇰

Hvidovre, Denmark

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