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Effectiveness of the Osteopathic Treatment in Patients With Nonspecific Cervical Pain

Primary Purpose

Manual Therapies, Neck Pain

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Osteopathic Manipulative Treatment (OMT) - Temp1
Combined Exercises
Sponsored by
Escola D'osteopatia De Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Manual Therapies focused on measuring osteopathy, osteopathic treatment, non-specific

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The sample will be formed by patients between the ages of 18 and 75 years, who present cervical pain of any intensity and duration, and with a minimum score of 10 points on the Neck Disability Index (NDI)14,15.

Exclusion Criteria:

  • Patients who present at the time of recruitment other pathologies or elements that may condition cervical pain, such as: acute shoulder tendinopathy, cervical radiculopathy, chronic diseases of general musculoskeletal involvement (Chronic Fatigue Syndrome and / or Fibromyalgia). Similarly, patients suffering from any type of vertiginous syndrome, who have suffered a whiplash in the last year or who are or have been under treatment for cervical pain in the last 3 months will also be excluded.

The taking of anti-inflammatories by the patient is not taken as a measure of exclusion. If the patient is under pharmacological treatment, it will be recorded and will be taken into account as a co-intervention. However, this treatment will not be modified under any circumstances nor will it be grounds for exclusion from the study.

Sites / Locations

  • IntegroSalus
  • AXIS
  • Clinica Osteopatia Horta

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Combined exercises+OMT weekly

Combined exercises+OMT once every 3 weeks

Combined exercises

Arm Description

This group will conduct a home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality This group will also receive Osteopathic Manipulative Treatment (OMT): exactly 3 sessions with a weekly frequency (with + -2 days of margin: between 5 and 9 days).

This group will conduct a home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality This group will also receive Osteopathic Manipulative Treatment (OMT): exactly 3 sessions at the rate of one session every 3 weeks (with + -2 days of margin: between 19-23 days).

This group will conduct a home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality.

Outcomes

Primary Outcome Measures

Effectiveness of osteopathic treatment
The effectiveness of osteopathic treatment will be assessed using two health questionnaires ("SF-36" and "NDI") compared to an exercise plan in patients with nonspecific cervical pain.

Secondary Outcome Measures

Temporal Frequency
The result of the treatment applied in different temporal frequencies will be compared.

Full Information

First Posted
September 16, 2019
Last Updated
November 5, 2019
Sponsor
Escola D'osteopatia De Barcelona
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1. Study Identification

Unique Protocol Identification Number
NCT04156308
Brief Title
Effectiveness of the Osteopathic Treatment in Patients With Nonspecific Cervical Pain
Official Title
Effectiveness of the Osteopathic Treatment in Patients With Nonspecific Cervical Pain: Randomized Controlled Pragmatic Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 2019 (Anticipated)
Primary Completion Date
February 2020 (Anticipated)
Study Completion Date
June 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Escola D'osteopatia De Barcelona

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
In Spain cervical pain affects practically 20% of the population annually, while globally it is estimated that between 22% and 77% of the population will suffer cervical pain at some point in their life. Prevalence increases with age, and is more common in women than in men (1.6: 1). Although the natural evolution of cervical pain tends to improve, the rates of recurrence and chronicity are high. And therefore it becomes an anatomical region of interest in relation to the assessment of the effectiveness and / or effectiveness of the osteopathic therapeutic approach. Different studies prove the efficacy of various manual therapy techniques applied on the cervical and / or upper dorsal region, suggesting significant positive changes in cervical pain and mobility levels in patients with nonspecific cervical pain. It is necessary to bear in mind that the reality of the osteopathic approach to the patient is not limited to the use of a single technique, but that the treatment is formed from a set of them. The ultimate goal is to restore mobility and functionality to a specific region, especially taking into account the concepts of individuality and holism. A pragmatic experimental comparative trial with three branches of study (osteopathic treatment with 2 different dosages versus active muscle exercise) is proposed.
Detailed Description
At the beginning of the 1st session, a battery of questions will be made as an anamnesis with the objective of evidencing possible risk factors at the therapeutic level. The presence of one or more risk factors will suppose the exclusion of the patient from the study. Next, a brief osteopathic musculoskeletal evaluation will be made to the patient. This exploration will follow a standardized protocol for all patients in the experimental groups (1 and 2). The tests to be carried out will be: Observation (standing patient): Assessment of the anterior projection of the head Assessment of the variation in the physiological curves of the spine Active test of the cervical spine with the patient in a sitting position. o Flexo-Extension / Rotations / Lateral inclinations Segmental test of joint mobility of the cervical and dorsal spine (patient in sitting and supine position) Passive mobility test of the cervical spine (patient in the supine position): Flexo-Extension / Rotations / Lateral inclinations The combination of exercises scheduled at home for all groups is based on the conclusions of different studies, and will consist of: Self-resisted active exercise in flexion, rotations and inclinations of the cervical spine. Active mobility in its maximum travel (without forcing pain) in flexion, rotations and inclinations of the cervical spine. Stretching upper trapezius muscles and scalenes. Active mobility in circumferential joints of the glenohumeral joint, and in flexo-extension of the thoracic spine. The work schedule will be carried out for 7 weeks, at a rate of 5 sessions per week. It will be the patient himself who will keep a diary record of the activity carried out during the weeks that the trial lasts. The diary will be facilitated by the therapists, and in it the exercises to be performed will be indicated. For groups 1 and 2, a total of 3 techniques selected from a list of 7 available techniques common to all centers will be applied in each session. The choice of techniques will be based on the results of the examination performed, the particularities of the patient and the clinical experience of the osteopath. In each session the techniques can change under the criteria of the osteopath. However, they will always be 3 and always within the list of available techniques. For groups 1 and 2, a total of 3 techniques selected from a list of 7 available techniques common to all centers will be applied in each session. The choice of techniques will be based on the results of the examination performed, the particularities of the patient and the clinical experience of the osteopath. In each session the techniques can change under the criteria of the osteopath. However, they will always be 3 and always within the list of available techniques. For groups 1 and 2, a total of 3 techniques selected from a list of 7 available techniques common to all centers will be applied in each session. The choice of techniques will be based on the results of the examination performed, the particularities of the patient and the clinical experience of the osteopath. In each session the techniques can change under the criteria of the osteopath. However, they will always be 3 and always within the list of available techniques. The OMT (Osteopathic Manipulative Treatment) techniques that may be applied will be the following: Technique of Inhibition of the suboccipital muscles Functional technique for the middle and deep cervical fascia High-speed cervical spine technique (Cervical wheel C1-C6) High-speed technique in the cervico-dorsal junction (prone position) High speed technique in dorsal column (D1-D12) - (Dog Technique) Muscle stretching technique of the diaphragm (supine decubitus) Thorax joint mobility technique (long lever) Main Variable: o Neck Disability Index (NDI). The investigators establish the minimum change to be detected (minimum clinically relevant change) at 5 points. The Spanish version of the NDI will be used, validated by Andrade Ortega et al.24 Secondary Variable: o Degree of general quality of life, through the "SF-36" Health Survey25. The data will be reported in the form of a report by the patient himself, who will receive via e-mail (whenever possible) or in printed form the questionnaire to be completed and will deliver to the same center in which the intervention has been carried out.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Manual Therapies, Neck Pain
Keywords
osteopathy, osteopathic treatment, non-specific

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A pragmatic experimental comparative trial with three branches of study (osteopathic treatment with 2 different dosages versus active muscle exercise) is proposed.
Masking
ParticipantOutcomes Assessor
Masking Description
A double masking is proposed. Three active interventions are compared. The patients will be blinded in relation to the study group they belong to, ensuring the masking of the participants. The data that is intended to be obtained for its analysis are of a self-reported nature and will be collected and administered by an external investigator not linked to the interventions, ensuring the masking of the evaluator. Due to the nature of the interventions, masking of therapists is not possible.
Allocation
Randomized
Enrollment
132 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Combined exercises+OMT weekly
Arm Type
Experimental
Arm Description
This group will conduct a home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality This group will also receive Osteopathic Manipulative Treatment (OMT): exactly 3 sessions with a weekly frequency (with + -2 days of margin: between 5 and 9 days).
Arm Title
Combined exercises+OMT once every 3 weeks
Arm Type
Experimental
Arm Description
This group will conduct a home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality This group will also receive Osteopathic Manipulative Treatment (OMT): exactly 3 sessions at the rate of one session every 3 weeks (with + -2 days of margin: between 19-23 days).
Arm Title
Combined exercises
Arm Type
Experimental
Arm Description
This group will conduct a home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality.
Intervention Type
Other
Intervention Name(s)
Osteopathic Manipulative Treatment (OMT) - Temp1
Intervention Description
A total of 3 techniques selected from a list of 7 available techniques common to all centers will be applied in each session. The choice of techniques will be based on the results of the examination performed, the particularities of the patient and the clinical experience of the osteopath. In each session the techniques can change under the criteria of the osteopath. However, they will always be 3 and always within the list of available techniques.
Intervention Type
Other
Intervention Name(s)
Combined Exercises
Intervention Description
A home-based pattern of combined exercises based on stretching, active anti-resisted exercises and joint mobility exercises focused on the cervico-dorsal and scapulo-thoracic regions. Whose clinical effectiveness has shown significant positive changes in pain levels and cervical functionality
Primary Outcome Measure Information:
Title
Effectiveness of osteopathic treatment
Description
The effectiveness of osteopathic treatment will be assessed using two health questionnaires ("SF-36" and "NDI") compared to an exercise plan in patients with nonspecific cervical pain.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Temporal Frequency
Description
The result of the treatment applied in different temporal frequencies will be compared.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The sample will be formed by patients between the ages of 18 and 75 years, who present cervical pain of any intensity and duration, and with a minimum score of 10 points on the Neck Disability Index (NDI)14,15. Exclusion Criteria: Patients who present at the time of recruitment other pathologies or elements that may condition cervical pain, such as: acute shoulder tendinopathy, cervical radiculopathy, chronic diseases of general musculoskeletal involvement (Chronic Fatigue Syndrome and / or Fibromyalgia). Similarly, patients suffering from any type of vertiginous syndrome, who have suffered a whiplash in the last year or who are or have been under treatment for cervical pain in the last 3 months will also be excluded. The taking of anti-inflammatories by the patient is not taken as a measure of exclusion. If the patient is under pharmacological treatment, it will be recorded and will be taken into account as a co-intervention. However, this treatment will not be modified under any circumstances nor will it be grounds for exclusion from the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Oscar Hernandez Amigo
Phone
+(34) 649.360.771
Email
oscarha@eobosteopatia.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oscar Hernandez Amigo
Organizational Affiliation
Escola Osteopatia de Barcelona
Official's Role
Principal Investigator
Facility Information:
Facility Name
IntegroSalus
City
Cabrils
State/Province
Barcelona
ZIP/Postal Code
08348
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Oscar Hernandez Amigo
Phone
+34.649.360.771
Email
oscarha@eobosteopatia.com
First Name & Middle Initial & Last Name & Degree
OSCAR HERNANDEZ AMIGO
Facility Name
AXIS
City
Sant Sadurní d'Anoia
State/Province
Barcelona
ZIP/Postal Code
08770
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
DAVID PUERTAS
Phone
+34.606.450.462
Email
dpuertas81@gmail.com
First Name & Middle Initial & Last Name & Degree
DAVID PUERTAS
Facility Name
Clinica Osteopatia Horta
City
Barcelona
ZIP/Postal Code
08031
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
EDGAR SEGARRA CALLIZO
Phone
+34.657.559.428
Email
edbandini@gmail.com
First Name & Middle Initial & Last Name & Degree
EDGAR SEGARRA CALLIZO

12. IPD Sharing Statement

Plan to Share IPD
No
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Effectiveness of the Osteopathic Treatment in Patients With Nonspecific Cervical Pain

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