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OpenTrials
Completed

NCT Number: NCT02703506

Effectiveness of a Pain Education Program on Chronic Neck Pain Patients

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

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Session of Pain Education programe

Other

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

Control Group

Other

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

Primary outcomes

  1. Visual Analog Scale

    Time frame: Change From Baseline in Pain Scores on the Visual Analog Scale at three months

    Measured by a Visual Analog Scale

Sponsors and collaborators

Lead sponsor

University of Alcala

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2017
First posted
Mar 9, 2016
Registry last updated
Dec 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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