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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04502927
Other study ID # GHR 1020
Secondary ID IDRCB 2019-A0295
Status Terminated
Phase N/A
First received
Last updated
Start date March 10, 2020
Est. completion date March 18, 2020

Study information

Verified date June 2021
Source Groupe Hospitalier de la Region de Mulhouse et Sud Alsace
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this monocentric prospective study is to evaluate the amplitudes and angular velocities of extension of the hand and wrist joints during passive mobilization by a physiotherapist in healthy subjects and stroke patients with spastic hands. Secondary objectives: - To compare amplitude and angular velocity values between the group of stroke patients and the group of healthy volunteers, - To compare amplitude and angular velocity values according to the two types of mobilization (i,e, thumb or fifth finger), - To assess pain due to mobilization in stroke patients.


Description:

Conduct of research: The realization of the measures will take place at the GHRMSA rehabilitation department. After receiving the written consent of the study participant, the physiotherapist will proceed with the passive mobilization of the spastic hand of the stroke patient or the dominant hand for healthy volunteers. Videos of the hand will be made using the Darfish system which will allow analysis of the primary endpoint. Two mobilizations will be performed for each participant, i.e. one for each type of medial or lateral grip. The order of mobilization will be determined by randomization.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date March 18, 2020
Est. primary completion date March 18, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Eligibility criteria of stroke patients with hand spasticity: Inclusion Criteria: - Age = 18 years old - First stroke diagnosed less than 3 months ago - Non-functional wrist defined by the Fugl-Meyer Assesment (FMA-EU) upper limb motor subscale with a score =45 - Wrist flexor spasticity defined by the Modified Tardieu Scale (MTS) with a rating =1 - Written informed consent Exclusion Criteria: - None Eligibility criteria of healthy volunteers: Inclusion criteria: - Age = 18 years old - Written informed consent Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Passive extension mobilization of the hand and wrist joints
The physiotherapist will proceed with the passive mobilization of the spastic hand of the stroke patient or the dominant hand for healthy volunteers. Two mobilizations will be performed for each participant, i.e. one for each type of medial or lateral grip. The order of mobilization will be determined by randomization.

Locations

Country Name City State
France Groupe Hospitalier de la Région de Mulhouse et Sud Alsace Mulhouse

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier de la Region de Mulhouse et Sud Alsace

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amplitude values Amplitude values will be calculated with the Dartfish® system 1 minute after intervention
Primary Angular velocity values Angular velocity values will be calculated with the Dartfish® system 1 minute after intervention
Secondary Mean amplitude of the two groups 1 minute after intervention
Secondary Mean angular velocity of the two groups 1 minute after intervention
Secondary Mean amplitude after mobilization with thumb abduction 1 minute after intervention
Secondary Mean angular velocity after mobilization with thumb abduction 1 minute after intervention
Secondary Mean amplitude after mobilization of the fifth finger 1 minute after intervention
Secondary Mean angular velocity after mobilization of the fifth finger 1 minute after intervention
Secondary Pain experienced by stroke patients before mobilisation Pain will be assessed by the Visual Analogue Scale (VAS) 1 minute before intervention
Secondary Pain experienced by stroke patients after mobilisation Pain will be assessed by the Visual Analogue Scale (VAS) 1 minute after intervention
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