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Clinical Trials/NCT04031937
NCT04031937CompletedNot Applicable

Sensory and Psychomotor Profile in Depression

Centre Hospitalier Esquirol2 sites in 1 country50 target enrollmentStarted: October 23, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
50
Locations
2
Primary Endpoint
% of patients with a failure at the gross motor test from the NP-MOT battery

Study Overview

Brief Summary

Despite a possible psychomotor retardation during a depressive episode, standardized psychomotor assessment is rare. So, other possible psychomotor disorders or neurological "soft signs" are not known in depression.

The investigator propose in this study to explore the psychomotor characteristics of patients with a major depressive disorder from the realization of a psychomotor assessment in comparison with adult without depressive disorder (control). It will be specifically assess muscle tone, gross motor skills, praxis, body schema and the body image and the perceptions.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • major depressive disorder according to the DSM-5
  • aged to 18 from 65 years old

Exclusion Criteria

  • psychiatric comorbidity (bipolar, addiction, eating disorder, personality disorder, obsessional compulsive disorder)
  • antipsychotic drug
  • taken care in psychomotor therapy previously
  • electroconvulsive therapy
  • medical history of neurologic disease, neurodevelopmental disorder, sensory disability
  • Constraint Hospitalization
  • under legal protection
  • lack of consent

Outcomes

Primary Outcomes

% of patients with a failure at the gross motor test from the NP-MOT battery

Time Frame: At inclusion

Scores at the NP-MOT psychomotor battery are considered. A failure is considered from a result \<1SD compared to the control group.

% of patients with a distinctive feature at the sensory profile questionnaire from the AASP

Time Frame: At inclusion

Scores at the AASP psychomotor battery are considered. A failure is considered from a result \<1SD compared to the control group.

% of patients with a failure at the muscle tone test from the NP-MOT battery

Time Frame: At inclusion

Scores at the NP-MOT psychomotor battery are considered. A failure is considered from a result \<1SD compared to the control group.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Centre Hospitalier Esquirol
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aude Paquet

Principal Investigator

Centre Hospitalier Esquirol

Study Sites (2)

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