Effect of Walking to the Operating Room on Preoperative Anxiety

NCT ID: NCT04908527

Last Updated: 2021-06-01

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-15

Study Completion Date

2019-11-21

Brief Summary

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The operating room environment can be a source of anxiety for the patient, including in the context of outpatient surgery for which anxiolytic medication is rarely used. This anxiety-induced effect can be reinforced by the patient's lack of active participation.

Some studies have already shown the feasibility of patient walking to the operating room (OR) and advantages this approach(Kojima and Ina 2002; Lack 2016; Nagraj et al. 2006).

Moreover, recovery room complications and pain have also been shown to be greater after varicose vein surgery in patients with significant preoperative anxiety (Scavee et al. 2016).

Therefore, the investigators decided to test the effects of walking to OR for patients admitted for outpatient surgery for varicose vein surgery.

Detailed Description

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Conditions

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Vein, Varicose

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Walk group

Patients walked to operating room (OR)

Group Type EXPERIMENTAL

Walking to OR

Intervention Type BEHAVIORAL

Patients, after being prepared for the OR, walk to the operating room

Bed group

Patients go to OR while in bed

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Walking to OR

Patients, after being prepared for the OR, walk to the operating room

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Outpatient minimal invasive laser therapy for venous insufficiency

Exclusion Criteria

* Inpatient surgery
* Invasive surgery
* Need for premedication
* Use of walking aid
* Non-French speaking patient
* Patient refusal
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Liege

OTHER

Sponsor Role lead

Responsible Party

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Claude Hallet

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Claude Hallet, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Liege

Locations

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Centre hospitalier universitaire de Liege

Liège, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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2019-122

Identifier Type: -

Identifier Source: org_study_id

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