Study of the Influence of POLD Manual Therapy in Fibromyalgia

Fibromyalgia Clinical Trial

Official title:

Study of the Influence of Manual Therapy According to the POLD Method Within a Pain Treatment Program in Fibromyalgia

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT03939416
• Other study ID #: Pold-fibromyalgia-udl
• Status: Suspended
• Phase: N/A
• Start date: July 1, 2024
• Est. completion date: March 30, 2025

Study information

• Verified date: March 2024
• Source: Omphis Foundation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical research aims to study the effects of the introduction of POLD manual therapy within the protocol of fibromyalgia

Description:

This research project aims to generate scientific evidence on the clinical results obtained in the treatment of fibromyalgia, which usually presents with pain and long-term disability, by applying a special form of manual physiotherapy called "POLD concept". This therapy is based on a passive, oscillatory mobilization, performed at a resonance frequency and applied throughout the time of the therapeutic session, on the vertebrae and the muscles of the back, without interruption. It is carried out on the initiative of the research team in "pain treatment", of the physiotherapy school of the University of Lleida, in collaboration with the Omphis Foundation and the clinical service of the Unity of Fibromyalgia of GSS (Hospital Universitarios de Santa María, Lleida)

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 50
• Est. completion date: March 30, 2025
• Est. primary completion date: December 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 25 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Patients diagnosed with Fibromyalgia

2. Patients over 25 years old and up to 65 years old, regardless of whether they are women or men.

3. Patients who present pain with a minimum value of 5 on the numerical pain scale from 0 to 10, at the time of beginning the study.

4. Presence of these symptoms in a long period (more than 6 months)

Exclusion Criteria:

1. Patients with a recent traumatic history.

2. Presence of an irradiation component of neurological origin to upper or lower limbs

3. Patients with neurological alterations, both central and peripheral.

4. Patients who are taking opioid-based analgesic medication.

5. Patients with severe spinal malformations.

6. That they are following any other type of treatment, whether manual or physical agents or alternative or complementary therapies.

7. That they have been treated with infiltrations or similar in a period of less than one year before beginning the study.

8. Patients with a serious psychiatric history such as schizophrenia or psychopathies.

9. Patients who have vestibular problems that do not tolerate oscillation.

10. Patients with heart failure

11. Existence of judicial process of disability

Related Conditions & MeSH terms

• Fibromyalgia
• Myofascial Pain Syndromes

Intervention

Other:
• Experimental
STANDART Physical exercise: degreed joint mobilization, self muscle elongation and postural correction. Sophrology: mental control of insomnia and painful perception Cognitive behavioral therapy: analysis of non-assertive relationship patterns or dependence, dysfunctional beliefs, as well as their consequences, psychoeducation of the disease. Strategies for pain management, anxiety, assertiveness and acceptance of the disease POLD Rhythmic transversal muscle mobilization in posterior chain musculature. General vertebral decompression from the sacrum and pelvis Metameric subcutaneous mobilization Rhythmic vertebral mobilization from the spinous processes.
• Control
STANDART Physical exercise: degreed joint mobilization, self muscle elongation and postural correction. Sophrology: mental control of insomnia and painful perception Cognitive behavioral therapy: analysis of non-assertive relationship patterns or dependence, dysfunctional beliefs, as well as their consequences, psychoeducation of the disease. Strategies for pain management, anxiety, assertiveness and acceptance of the disease

Locations

Country	Name	City	State
Spain	Specialized hospital unit of fibromyalgia and SD of conical fatigue of L'Hospital Universitari de Santa María (GSS)	Lleida	Catalonia

Sponsors (2)

Lead Sponsor	Collaborator
Omphis Foundation	Universitat de Lleida

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Demographic data	The following data will be recorded: age, sex, race, children, study start date and final date.	Participants will be followed for the duration of treatment application, an expected average of 8 weeks.
Primary	Level of Pain: VAS	We will use the Visual Analog Pain Scale (VAS), consisting of a line of 10 cm, whose left end coincides with the value 0 (absence of pain) and the right end with the value 10 (maximum pain imaginable), without reference marks intemediate The patient will mark a point in the line corresponding to his pain at the time of the test, the measurement of the centimeters from the left edge will indicate the analogical score of his pain between 0 and 10.	Participants will be followed for the duration of treatment application, an expected average of 8 weeks.
Primary	Quality of pain: The Mc Gill pain questionnaire	The Mc Gill pain questionnaire comprises 62 descriptors distributed in 15 classes and, in turn, in 3 dimensions (sensory, affective and evaluative).; A value of pain is obtained for each dimension: sensory pain intensity (VID (S), affective pain intensity (VID (A)) and evaluative pain intensity (VID (E)) The sensory component is evaluated in 7 subclasses. The patient mark one or no descriptor of each subclass, if he scores 1 he scores 1 and if he does not mark none he scores 0. The score of the VID (S) is obtained adding and will be, therefore, between 0 and 7. The affective dimension includes subclasses 8 to 13 and its score ranges from 0 to 6. The evaluative dimension corresponds to subclass 14 and the score of it will be 0 or 1. From the sum of the three, the total score (VID (T)) is obtained, from 0 to 14. In addition, the current pain intensity (VIA) is scored from subclass 15, the score is 0-no pain, 1-mild, 2-annoying, 3-intense, 4-strong, 5-unbearable.	Participants will be followed for the duration of treatment application, an expected average of 8 weeks.
Primary	Pain interference: We use the Brief Pain Inventory	We use the Brief Pain Inventory that gives two main scores: a pain severity score and a pain interference score. The pain severity score is calculated from the four items about pain intensity. Each item is rated from 0, no pain, to 10, pain as bad as you can imagine, and contributes with the same weight to the final score, ranging from 0 to 40. The pain interference score corresponds to the item on pain interference. The seven sub items are rated from 0, does not interfere, to 10, completely interferes, and contributes with the same weight to the final score, ranging from 0 to 70. The first item, pain drawing diagrams (painful and most painful areas) do not contribute to the scoring	Participants will be followed for the duration of treatment application, an expected average of 8 weeks.