Early Occupational Therapy in Intensive Care: Feasibility of Implementation

NCT ID: NCT04186611

Last Updated: 2020-02-25

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

14 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-14

Study Completion Date

2019-12-06

Brief Summary

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The objective of the study is to assess the feasibility of early daily occupational therapy intervention within an interdisciplinary team in an intensive care unit of a Swiss university hospital.

Detailed Description

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Conditions

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Occupational Therapy Intensive Care

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Early daily occupational therapy intervention

A daily occupational therapy intervention is performed with the patients included. The intervention will consist of assessment as well as early positioning and/or rehabilitation in activities of daily living.

Group Type EXPERIMENTAL

early occupational therapy

Intervention Type OTHER

The intervention will be the one usually carried out but earlier and on a daily basis. It will consist of the initial assessment and then positioning and/or carrying out activities of daily living.

The daily duration of the intervention will be about 45 minutes to 1 hour. The overall duration of the intervention will be determined according to the objectives and will be at most equal to the time of stay in the intensive care unit.

Interventions

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early occupational therapy

The intervention will be the one usually carried out but earlier and on a daily basis. It will consist of the initial assessment and then positioning and/or carrying out activities of daily living.

The daily duration of the intervention will be about 45 minutes to 1 hour. The overall duration of the intervention will be determined according to the objectives and will be at most equal to the time of stay in the intensive care unit.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* ≥ 18 years old.
* Hospitalized at SMIA for at least 48 hours.
* Stable patient: hemodynamically stabilized patient (norepinephrine dose \< 15 mcg/min iv), respiratory (P/F ratio \> 150) and neurological (Glasgow Coma Scale \> 8).

Exclusion Criteria

* contraindication to occupational therapy
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Vaudois

OTHER

Sponsor Role lead

Responsible Party

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Marie-Gabrielle Wick Brasey

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Centre Hospitalier Universitaire Vaudois

Lausanne, Canton of Vaud, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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ERGO-PRE-SI_2019-00867

Identifier Type: -

Identifier Source: org_study_id

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