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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05634486
Other study ID # 1633-N-21
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 15, 2022
Est. completion date October 31, 2023

Study information

Verified date February 2024
Source Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Randomized-clinical trial of multidisciplinary approach versus psychoeducation in patients with functional movement disorders: impact to their quality of life and their caregivers' quality of life. Patients with functional movement disorders are randomized in two arms of a one-month treatment (physiotherapy + cognitive-behavioral therapy versus psychoeducational as sham intervention) with a 3-month and 5-month follow-up where the investigators will measure the change in the patients' and caregivers' quality of life. Movement disorders specialists will review the severity of symptoms as blinded raters in the 3th-month and 5th-month follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 31, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of Functional Movement Disorders (Espay and Lang, 2015) - Patients should be 18 years old or older and capable of giving consent to freely and willingly participate in the study. - Patients should be able to attend the one-month ambulatory regime and follow-up visits. Exclusion Criteria: - Any condition that avoid the patient from giving free consent to participate in the study. - Any non-controlled psychiatric disorders

Study Design


Intervention

Behavioral:
Multidisciplinary therapeutic approach (physiotherapy plus cognitive-behavioral therapy)
Patients randomly allocated to this arm of intervention will receive an ambulatory therapy regime of twelve 60-minute physiotherapy sessions plus four 60-minute psychotherapy sessions throughout one month of treatment
Other:
Psychoeducation (Sham intervention)
Patients randomly allocated to this arm of intervention will receive an ambulatory regime of four 60-minute non-organized psychoeducational sessions throughout one month of treatment.

Locations

Country Name City State
Spain Hospital Universitario Virgen del Rocío / Instituto de Biomedicina de Sevilla (IBiS) Sevilla

Sponsors (2)

Lead Sponsor Collaborator
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla Fundación Caser

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life in patients with functional movement disorders measured by The 5-level EQ-5D version (EQ-5D-5L) - EQ visual analogue scale Change in the patients' quality of life measured by changes in EQ-5D-5L - the EQ visual analogue scale (EQ VAS). 3th-month and 5th-month follow-ups
Primary Quality of Life in patients with functional movement disorders measured by The 5-level EQ-5D version (EQ-5D-5L) - EQ-5D descriptive system. Change in the patients' quality of life measured by changes in EQ-5D-5L - EQ-5D descriptive system. The digits for the five dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression) can be combined into a 5-digit number that describes the patient's health state. 3th-month and 5th-month follow-ups
Primary Quality of Life in patients with functional movement disorders measured by the 36-Item Short Form Health Survey (SF-36) Change in the patients' quality of life measured by changes in SF-36 3th-month and 5th-month follow-ups
Secondary Quality of Life in caregivers of patients with functional movement disorders Change in the caregivers' quality of life measured by changes in the Zarit Caregiver Burden Interview 3th-month and 5th-month follow-ups
Secondary Severity of functional neurological symptoms of patients with functional movement disorders measured by Clinical Global Impressions (CGI) Scale Change in the patients' symptoms severity measured by changes in the Clinical Global Impressions (CGI) Scale - Severity 3th-month and 5th-month follow-ups
Secondary Improvement of functional neurological symptoms of patients with functional movement disorders Improvement of the patients' symptoms severity measured by the Clinical Global Impressions (CGI) Scale - Improvement 3th-month and 5th-month follow-ups
Secondary Severity of functional neurological symptoms of patients with functional movement disorders Change in the patients' symptoms severity measured by changes in the simplified-Functional Movement Disorders Rating Scale 3th-month and 5th-month follow-ups
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