Effectiveness of a Pain Education Program on Chronic Neck Pain Patients

Neck Pain Clinical Trial

Official title:

Effectiveness of a Pain Education Program on Chronic Neck Pain Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02703506
• Other study ID #: OE22/2015
• Status: Completed
• Phase: N/A
• Start date: March 2016
• Est. completion date: July 2017

Study information

• Verified date: December 2023
• Source: University of Alcala
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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

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)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: July 2017
• Est. primary completion date: December 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

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.

Related Conditions & MeSH terms

• Neck Pain

Intervention

Other:
• Session of Pain Education programe
Five group sessions of patient education pain of 60-120 minutes one for 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

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Alcala

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Analog Scale	Measured by a Visual Analog Scale	Change From Baseline in Pain Scores on the Visual Analog Scale at three months