Use of a Fabric Mattress Cover for Patient Comfort

NCT ID: NCT01545089

Last Updated: 2015-03-26

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

174 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-07-31

Study Completion Date

2013-03-31

Brief Summary

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The main objective of this research project is to measure the impact on patient satisfaction of the use of a fabric mattress cover fabric on a bedsheet protecting a plastic mattress.

Detailed Description

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Conditions

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Patient Comfort

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Mattress protector days 1,2

A mattress protector is placed in the bed for the first two days and then removed for days 3 and 4.

Group Type EXPERIMENTAL

Mattress protector for days 1 and 2

Intervention Type OTHER

A mattress protector is placed in the bed for the first two days and then removed for days 3 and 4.

Mattress protector days 3,4

A mattress protector is not placed in the bed for the first two days and then added to the bed for days 3 and 4.

Group Type EXPERIMENTAL

Mattress protector for days 3 and 4

Intervention Type OTHER

A mattress protector is not placed in the bed for the first two days and then added to the bed for days 3 and 4.

Interventions

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Mattress protector for days 1 and 2

A mattress protector is placed in the bed for the first two days and then removed for days 3 and 4.

Intervention Type OTHER

Mattress protector for days 3 and 4

A mattress protector is not placed in the bed for the first two days and then added to the bed for days 3 and 4.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The patient must have given his/her informed and signed consent
* The patient must be insured or beneficiary of a health insurance plan
* The patient has a planned hospitalization \> 4 days
* The patient is "movable" within 48 hours

Exclusion Criteria

* The patient is participating in another study
* The patient is in an exclusion period determined by a previous study
* The patient is under judicial protection, under tutorship or curatorship
* The patient refuses to sign the consent
* It is impossible to correctly inform the patient
* The patient is pregnant
* The patient is breastfeeding
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Nīmes

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Luc Duwig, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Nîmes

Locations

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CHU de Nîmes - Hôpital Universitaire Carémeau

Nîmes, Gard, France

Site Status

Countries

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France

Other Identifiers

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2011-A01595-36

Identifier Type: OTHER

Identifier Source: secondary_id

LOCAL/2011/LD-02

Identifier Type: -

Identifier Source: org_study_id

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