Predictability of the Ability to Perform an Emergency Stop With Disorders of the Hip

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2015-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Several studies exist on patient performance in drive simulators especially around and after surgery. Recommendations concerning the ability to drive preoperatively are based on these studies, which generated their data using drive simulators. However, in all the datasets driving performance remains highly individual. Since a drive simulator is not readily available in normal general practitioner surgeries it would be helpful to have convenient clinical tests to evaluate a patients individual ability to perform an emergency stop. This study aims at evaluating different possibilities how such performance might be predicted. Patients with hip osteoarthritis and patients who have received total hip arthroplasty are tested clinically and their results are compared with the gold standard experiment - a drive simulator.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Predictability of the Ability to Perform an Emergency Stop

NCT02175160

Osteoarthritis Total Knee Arthroplasty

COMPLETED NA

Immediate Post-THA Functional Assessment

NCT04928924

Arthritis of Hip

UNKNOWN

Rehabilitation in Total Hip Arthroplasty Through a Mobile Application

NCT06606158

Total Hip Arthroplasty

COMPLETED

Change of Cognitive Performance Through Hip Replacement

NCT02997891

Osteoarthritis, Hip

UNKNOWN

Evaluation of Locomotor Activity Before and After Total Hip Replacement in Patients With Hip Osteoarthritis.

NCT02042586

Hip Osteoarthritis Indication for Total Hip Replacement

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteoarthritis Total Hip Arthroplasty

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Braking and functionality with hip osteoarthritis

Cohort testing of driving performance in a drive simulator and correlation with clinical functionality in patients with hip osteoarthritis

Group Type EXPERIMENTAL

Braking and functionality

Intervention Type OTHER

Braking and functionality with hip arthroplasty

Cohort testing of driving performance in a drive simulator and correlation with clinical functionality in patients with total hip arthroplasty

Group Type EXPERIMENTAL

Braking and functionality

Intervention Type OTHER

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Braking and functionality

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 18-85 y
* valid driving license
* male and female
* Hip Osteoarthritis, Total hip arthroplasty
* capability to walk with or without a walking stick

Exclusion Criteria

* myocardial infarction/Apoplexia \< 6 months
* Total hip arthroplasty \<5 weeks
* New York Heart Association 3/4
* lacking drivers' license
* peripheric sensomotor deficit \<3/5 British Medical Research Council
* new fracture of the lower extremity or spine
* systemic or metastasised Cancer
* drug intake with centrally acting substances known to affect reaction time (Opioids, e.g. Tramadol, oxycodone, morphine, Til

Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes