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Clinical Trials/NCT02439463
NCT02439463CompletedNot Applicable

Traumatic Below-knee Amputees With Prosthetics: Health-related Quality of Life and Locomotor Capabilities

Helsinki University Central Hospital1 site in 1 country26 target enrollmentStarted: June 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
26
Locations
1
Primary Endpoint
Locomotor capabilities of traumatic below-knee amputees with prothesis

Study Overview

Brief Summary

The present study assesses the health-related quality of life and the locomotor capabilities major traumatic lower limb amputees who use prosthesis.

Detailed Description

A cross sectional study based on a retrospective review of prosthetic using major traumatic lower limb amputees' demographic and clinical details together with HRQoL and locomotor capabilities patient-reported outcome measures.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Below-knee prosthesis users with amputation due to trauma

Exclusion Criteria

  • Patients with no prosthesis

Outcomes

Primary Outcomes

Locomotor capabilities of traumatic below-knee amputees with prothesis

Time Frame: 2-5 years

The health-related quality of life measured by HRQoL score

Time Frame: 2-5 years

Secondary Outcomes

  • Prothesis Evaluation Questionnaire(2-5 yeats)
  • 15D health-related quality of life instrument(2-5 years)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jussi Repo

MD

Helsinki University Central Hospital

Study Sites (1)

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