Towards an Objectivation of the Therapeutic Effect of a Rocking Movement

NCT ID: NCT02834598

Last Updated: 2020-09-07

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

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2017-10-31

Brief Summary

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The study evaluates the benefits of a rocking movement on well-being and attention, through high-density electroencephalography recordings. The effect of the rocking movement is compared to a seated position and a lying position.

Detailed Description

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Conditions

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Rocking Movement

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Rocking movement

Participant is lying in a hammock with a rocking motion. Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Group Type EXPERIMENTAL

high-density electroencephalography

Intervention Type DEVICE

Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Lying position

Participant is lying in a hammock with no rocking motion. Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Group Type ACTIVE_COMPARATOR

high-density electroencephalography

Intervention Type DEVICE

Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Seated position

Participant is sitting on a chair. Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Group Type ACTIVE_COMPARATOR

high-density electroencephalography

Intervention Type DEVICE

Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Interventions

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high-density electroencephalography

Cerebral measurements from high-density electroencephalography while standard and deviant sounds are presented to the participant.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Right handed
* Informed consent

Exclusion Criteria

* Pregnancy
* subjects with analgesic treatment
* subjects dependent on psychotropic substances
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Centre Hospitalier Universitaire de Besancon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Régis Aubry, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Service douleur - soins palliatifs

Other Identifiers

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API/2012/27

Identifier Type: -

Identifier Source: org_study_id

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