Therapeutic Exercise to Treat Neuropathic Pain

Fabry Disease Clinical Trial

— Aps  

Official title:

Therapeutic Exercise to Treat Neuropathic Pain in Patients With Chronic Lisosomal Injuries: Learning and Service Project

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04050137
• Other study ID #: PI19/205
• Status: Completed
• Phase: N/A
• Start date: May 2, 2019
• Est. completion date: December 14, 2020

Study information

• Verified date: December 2020
• Source: Universidad de Zaragoza
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A quasi-experimental, prospective clinical trial with pre and post intervention measurements, whose porpuose is assess the efficacy of a therapeutic exercise protocol to treat neuropathic pain in Fabry Disease.

Description:

There take part in this study women or men aged between 18 and 65 years, with a diagnosys by a physician specializing in Fabry disease with FabryScan. Patients must present a stable evolution, with a scoring system of disease severity (DS3) that must be less than 8 points per year in the last 2-3 years and they have to presence of neuropathic pain with a score greater than or equal to 4 in the questionnaire "Douleur neuropathique (DN4)".

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: December 14, 2020
• Est. primary completion date: December 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 16 Years to 65 Years

Eligibility

Inclusion criteria:

• Female or male patients between 18 years and 65 years.

• Patients diagnosed by a doctor specializing in Fabry disease with FabryScan.

• Fabry's disease must have a stable evolution, with a disease severity scoring system (DS3) that must be less than 8 points per year in the last 2-3 years.

• Presence of neuropathic pain with a score greater than or equal to 4 in the "Douleur neuropathique (DN4)" questionnaire.

Exclusion criteria:

• Patients with an acute cardiovascular disease or with a heart or kidney transplant.

• Subjects with acute orthopedic problems that limit their participation in the study.

• Subjects with cognitive impairments that prevent them from filling in the questionnaires or understanding the exercises to be performed.

Related Conditions & MeSH terms

• Fabry Disease
• Gaucher Disease
• Neuralgia

Intervention

Other:
• Therapeutic Exercise
Patients who meet the inclusion criteria and who want to carry out the workshops, fill out an informed consent explaining the procedure to be followed and accepting the cessation of data to carry out the study. Patients will be divided into 2 working groups (approximately 10 patients in total, in a Gaucher disease group and in another Fabry disease). The workshops will be held at the foundation twice a month in sessions of 45 minutes of work for 3 months (May, June, July 2019). In these sessions the physiotherapists will show the new exercises to the patients. The exercises that are taught in that session should be done at home 3 times a week. In addition, a document will be delivered with the exercises to be carried out and the frequency and intensity of execution. The workshops will be guided at all times by a physiotherapist specialized in therapeutic exercise and EDL.

Locations

Country	Name	City	State
Spain	FEETEG	Zaragoza

Sponsors (4)

Lead Sponsor	Collaborator
Universidad de Zaragoza	fundación española para el estudio y tratamiento de la Enfermedad de Gaucher y otras lisosomales, Fundación Ibercaja, Fundación San Valero

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Neurophatic pain	DN4. This tool allows to estimate the probability of neuropathic pain of the patient in a valid and reliable way. It consists of 4 questions with 10 items to fill out. The researcher directly asks the patient and it is the investigator who completes the questionnaire. To each item, you must provide a "yes" or "no" answer; the "yes" is worth 1 point and the "no" is worth 0 point. At the end of the questionnaire, the investigator counts the patient's score on 10. If the patient's score is equal to or greater than 4 out of 10, the test is positive.	8 weeks
Secondary	Functionality	Arm Functionality DASH. The DASH questionnaire is a tool for assessing and measuring the functionality of the upper limb that the patient perceives during daily activities. This questionnaire is used in several studies with patients with disabilities in the hand, elbow and shoulder. It is valid, reliable and capable of detecting changes.	8 weeks
Secondary	Legs' strenght	Test of rising and sitting of the chair during 30 seconds as many times as possible.	8 weeks
Secondary	Strenght of the extensor muscless of the trunk	BST. Biering-Sorensen test.The test is to keep the trunk in prone position as long as possible to assess the resistance of the trunk extensor musculature.	8 weeks
Secondary	Strenght of the inclination muscless of the trunk	TSB. Test Side-Bridge assesses the resistance of the inclination muscles or lateral flexors of the trunk. In it the participants are placed in lateral recumbency on their dominant side in a mat. In this position, the participants support themselves with the elbow and the forearm of their dominant side and raise the pelvis until the trunk is aligned with the lower extremities. The test consists of maintaining the referred position as long as possible.	8 weeks
Secondary	Strenght of the flexor muscless of the trunk	ITo. To assess the resistance of the flexor muscles of the trunk, the participants are placed supine with the hips and knees bent at 90º. The participants flex the upper part of the trunk until they touch the thighs with the elbows, keeping the cervical spine in a neutral position.	8 weeks
Secondary	Visual Analogue Scale	VAS. The analog visual pain scale is a tool that is used to assess the pain perceived by the patient in a valid and reliable way.; It is an instrument for measuring the intensity of pain that represents a horizontal line of 10 cm with a score of 0 to 10, where 0 represents non-pain and 10 unbearable pain.; The patient should place a vertical line on the horizontal line of the scale where he places his pain intensity.	8 weeks
Secondary	Hospital, anxiety and depression questionnaire	HADS. This questionnaire allows to evaluate the psychosocial factors of the patient, through 14 questions with two subscales of 7 questions (one subscale on anxiety and the other on depression); The patient must answer one of the 4 items of each question without much reflection to have a real answer of how he was during the past week. The intensity or frequency of symptoms is evaluated with a Likert scale ranging from 0 to 3. In each subscale (anxiety and depression) the points are added and interpreted as such: 0-7 points: normal; 8-10 points: doubtful and higher than 11: clinical problem. This tool is validly and reliably used in clinical practice.	8 weeks
Secondary	SF-36	This questionnaire assesses the quality of life perceived by the patient. It is widely used in clinical practice and is approved as valid and reliable. There are 36 questions with 2,3,5 or 6 items in each question and with an assessment between 0 and 100. The questions assess physical function, function limitations due to physical health problems, body aches, general health, vitality, social functioning and emotional and mental health problems	8 weeks
Secondary	Semmes Weinstein monofilament test	The Semmes Weinstein monofilament test is a tool that evaluates tactile and pressure sensitivity in a valid and reliable way. A nylon filament attached to a handle is used which, when folded, applies a constant pressure of 10g. The investigator applies the monofilament perpendicular to the skin with increased pressure until the monofilament bends and without supporting it for more than 1 or 2 seconds.; The test will be performed on the sole of the foot in 4 points: the first toe, the base of the first, third and fifth metatarsals.; When the patient notices something, he puts a 1 and a 0 if he does not notice something. The sensitivity index is obtained with the sum of the values and is considered a sensitive patient only when it has a score of 8/8.	8 weeks