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Effectiveness of a Pain Education Program on Chronic Neck Pain Patients

Effectiveness of a Pain Education Program on Chronic Neck Pain Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02703506
Enrollment
44
Registered
2016-03-09
Start date
2016-03-31
Completion date
2017-07-31
Last updated
2023-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Brief summary

This project aims to study the effectiveness of a pain education program in the improvement of chronic pain and disability/impairment. Assuming the definition established in the United States in 1975 on the fourth working group of the National Conference on Preventive Medicine: Health education must be a process that informs, motivates and helps people to adopt and maintain practices and healthy lifestyles, environmental advocates changes necessary to facilitate these objectives and professional training and directs research towards the same objectives. Once the need of educating patients is stablished on subjects with diseases, it is necessary to encourage them to actively participate on the control of them and to achieve significant improvement of adherence

Detailed description

BACKGROUND AND PURPOSE: Patient education over the knowledge of pain causes and perpetuating psicosocial factos, so as a gradual physical therapy intervention may success in modifying habits, and consequently emotional state and behaviour in order to maintain or recover subject's social participation being this program effective in pain diminution over chronic neck pain. Main goal: To evaluate the effectiveness of a pain education program for patients with chronic neck pain, to decrease the intensity of pain in front of one physiotherapy program (TENS and exercise) Experimental group: Will receive five group sessions of 60-120 minutes twice a week with a maximum of 10 participants. Control group: Five individual sessions twice a week, will be performed of transcutaneous electrical nerve stimulation (TENS) on neck area an exercises. OUTCOMES Primary outcome * Intensity of pain, measured by the visual analog scale: VAS. The mean of the values wil be calculated described in the assessment, the mean of the last week was also compiled. * The degree of neck disability/impairment measured using the Northwick Park Pain Questionnaire (NPPQ)

Interventions

OTHERSession of Pain Education programe

Five group sessions of patient education pain of 60-120 minutes one for week with a maximum of 10 participants.

OTHERControl Group

Five individual sessions twice a week, will be performed of transcutaneous electrical nerve stimulation (TENS) on neck area an exercises

Sponsors

University of Alcala
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Subjects over 18 years old * Subjects diagnosed with chronic neck pain.

Exclusion criteria

* Patients with acute and subacute neck pain. Those presenting inflammatory, neurologic, rheumatic or heart disease or pacemakers. Patients with severe osteoporosis, fractures, dislocations, vertebrobasilar insufficiency, infection, metastatic tumor, pre and post-surgical etiology recent (less than one year after the intervention). Psychopathology patients diagnosed by their doctor. Subjects who do not understand or speak the Spanish language.

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog ScaleChange From Baseline in Pain Scores on the Visual Analog Scale at three monthsMeasured by a Visual Analog Scale

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026