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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06253273
Other study ID # CamiloJcUFYS
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 15, 2024
Est. completion date November 30, 2024

Study information

Verified date April 2024
Source Camilo Jose Cela University
Contact Edurne Úbeda D'Ocasar
Phone +34 918 153131
Email eubeda@ucjc.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Fibromyalgia is a chronic syndrome that causes fatigue, sleep disorders and generalized chronic pain in different parts of the body. This pathology is more prevalent in women and is generally not attributed to any specific cause. This observational study aims to describe some important and health-related factors in patients with fibromyalgia. Participants will have to fill out questionnaires related to sleep, anxiety, impact of the disease and sarcopenia index, and will then take tests related to grip strength for the upper limbs and dynamometry in the lower limbs. We will also employ the use of ultrasound to evaluate architectural measurements. Last but not least, we cannot forget the pain measurements that are so necessary in this study population.


Description:

Through the present research study we intend to analyze not only the health status of our sample but also to correlate the parameters analyzed with factors related to sarcopenia. Through the data collection that will be carried out we can analyze variables as essential as pain, anxiety and depression, impact of the disease, agility, strength, anthropometric measurements, sleep and muscular architectural measurements by means of ultrasound in which we can analyze the fatty infiltration of structures such as the vastus lateralis, rectus anterior and vastus medius that allow us to obtain data that can define the characteristics of patients with fibromyalgia.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date November 30, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Diagnosed with FM - aged between 18 and 75 years - agree to participate and sign the informed consent. Exclusion Criteria: - who do not have recent surgeries - patients with reduced mobility - adequate level of comprehension to be able to answer the questionnaires that will be provided in the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Camilo Jose Cela University

Outcome

Type Measure Description Time frame Safety issue
Primary Algometer Algometer points: Using an algometer, the pain threshold at each tender point is measured in kg/cm. The higher the value obtained, the less pain the subject has. baseline
Primary VAS Visual Analogic Scale: this self-referenced scale ranges from 0 to 10 where 0 is no pain at all and 10 indicates the worst possible pain endured. The higher the score, the greater the pain baseline
Primary Circometry Contour measurements: The contour of the segment selected for the study will be measured using a tape measure. It is measured in centimeters. the greater the number of centimeters, the greater the diameter and therefore the worse the condition or greater the liquid retention of the subject. baseline
Primary Dynamometer upper limb grip strength: this measuring tool measures upper limb grip strength. the higher the value, the better the subject's state of strength baseline
Primary Iso-pull lower limb strength: this measuring tool measures the strength of lower limbs. the higher the value, the better the subject's state of strength. baseline
Primary Chair test number of squats for 30 seconds: this test consists of seeing how many squats can be done in the test time. The greater the number of squats, the better the subject will be. baseline
Primary Timed up and go balance test: The Timed Up and Go Test is an easy-to-use test to assess the risk of falls.The shorter the test time, the lower the risk of falling. baseline
Primary anthropometric measurements anthropometric measurements with the uso of the Tanita baseline
Primary muscular architectural stockings taking architectural muscle averages using an ultrasound scanner baseline
Primary Pittsburgh sleep quality questionnaire: This test has values from 0 to 21 points maximum. It is interpreted that the higher the score, the worse the quality of sleep. baseline
Primary FIQ fibromyalgia impact questionnaire: The total FIQ score is between 0-100 as each of the items has a score of 0-10 once adapted. Thus, 0 represents the highest functional capacity and quality of life and 100 the worst state. baseline
Primary SARC-F questionnaire to measure sarcopenia risk: The SARC-F is a quick and easy instrument for detecting the risk of sarcopenia, which asks the degree of difficulty an older adult has in performing 4 functional activities. A score greater than 4 indicates risk of sarcopenia. baseline
Primary HADS to evaluate emotional distress in patients with different chronic conditions, assessing cognitive and behavioral symptoms of anxiety and depression. The HADS is composed of two subscales: Depression and Anxiety, each with seven items. The score of each subscale can vary between 0 and 21, since each item presents four response options, ranging from absence/minimal presence = 0, to maximum presence = 3. baseline
Secondary socio-demographic variables socio-demographic variables (age, weight, height, medication intake, marital status, employment status, etc. baseline
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