Sensory Characteristics and Psychosocial Factors Related With Non-specific Neck Musculoskeletal Pain Chronification

NCT ID: NCT04330573

Last Updated: 2021-01-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

68 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-04-15

Study Completion Date

2021-01-22

Brief Summary

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Chronic pain is commonly defined as any pain which lasts more than 12 weeks. Chronic non-specific neck pain (CNSNP) has no specific underlying disease causing the pain. There are neurophysiological factors that may modulate pain response and perception in the central nervous system, producing sensory changes such as the presence of temporal summation (TS) and pressure, cold or heat hyperalgesia. TS describes the progressive increase in reported pain intensity as a function of repeated noxious stimulation (e.g. thermal, electrical or mechanical). TS and hyperalgesia are measured through quantitative sensory tests (QST) where pain pressure thresholds (PPT) are measured with an algometer. The current evidence show that PPTs are significantly lower compared to healthy subjects and the association between PPTs, pain intensity and disability are inconsistent. Further, there are psychosocial factors (catastrophizing, kinesiophobia, stress…) that may influence the pain experience. This psychosocial factors associated with chronic pain are not systematically collected in the QST literature complicating the interpretation of data. The objectives of this study are 1) to determine disability, sensory (TS and PPTs) and psychosocial changes (kinesiophobia, catastrophizing, sleep quality, life quality, stress and anxiety) in the natural evolution or in the result of physiotherapy treatment in CNSNP individuals, 2) to study the correlations between disability, psychosocial and sensory factors and 3) to observe if there is a homogeneity between the subjects.

Detailed Description

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Conditions

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Neck Pain

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Chronic Non-Specific Neck Pain

Patients with chronic non-specific neck pain. No interventions

No intervention. Observational study

Intervention Type OTHER

Observational study

Control/Healthy Group

Volunteers without pain. No interventions.

No intervention. Observational study

Intervention Type OTHER

Observational study

Interventions

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No intervention. Observational study

Observational study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. age between 18 and 65 years;
2. capable to understand, write, and speak in Spanish;
3. having suffered neck pain during the last 12 weeks at least;
4. pain localized in the neck region with or without pain radiation;
5. Negative Spurling test;
6. Negative Self-Administered Leeds Assessment of Neuropathic Symptoms and Signs (S-LANSS);
7. Negative Upper Limb Tension Test for the median nerve;
8. PainDetect test with non-neuropathic pain result. .

Exclusion Criteria

1. Presence of red flag as reported in the medical history (i.e. tumor, fracture, metabolic diseases, rheumatoid arthritis, osteoporosis);
2. Neck pain with cervical radiculopathy;
3. fibromyalgia syndrome,
4. previous neck surgery;
5. currently undergoing any type of pain treatment or having received physical therapy in the previous 3 months.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hospital General de la Defensa en Zaragoza

UNKNOWN

Sponsor Role collaborator

Universidad San Jorge

OTHER

Sponsor Role lead

Responsible Party

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Pablo Herrero Gallego

Dr. Pablo Herrero, PT, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hospital General de la Defensa

Zaragoza, , Spain

Site Status

Countries

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Spain

Other Identifiers

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CNSNP-USJ

Identifier Type: -

Identifier Source: org_study_id

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