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Prevention of Neck Pain in Adults With a Back School-Based Intervention.

U

University of Vigo

Status

Completed

Conditions

Exercise Therapy
Primary Prevention
Neck Pain
Health Education

Treatments

Behavioral: Back School

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The study consists of a theoretical and practical intervention based on the Back School. This intervention will be carried out over 8 weeks with a frequency of two sessions per week, for a total of 16 sessions of 45 minutes duration. Of all the sessions, 14 had a practical focus (strength and stretching exercises) and the other two had a theoretical focus (self-management techniques and pain neuroscience education).

The clinical practice guidelines highlight the importance of neck pain prevention through exercise an education. There are previous studies of the effects of theoretical and practical programmes based on back school on the lumbar region but not on the cervical region.Therefore, the main aim of this innovative study is to to investigate the effects of a Back School based intervention on the prevention of neck pain and as secondary objectives to investigate the effects on neck flexor and extensor strength as well as scapular stability. The hypothesis is that this BS-based intervention would have positive effects on neck pain prevention, neck strength and scapular stability.

Enrollment

57 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Ages 18 - 65 years old.
  • Not have had neck pain in the last 6 months.

Exclusion criteria

  • Previous neck or shoulder surgery, cervical radiculopathy/myelopathy, history of the whiplash injury.
  • Taking any medication or having any musculoskeletal, rheumatic, metabolic, cardiological, cognitive disorder or neurological disorder.
  • Missing more than two Back School sessions.
  • Not being able to attend the measurement sessions.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

57 participants in 2 patient groups

Experimental group
Experimental group
Description:
Intervention based on the Back School was carried out for 8 weeks with a frequency of two sessions per week, with a total of 16 sessions lasting 45 min.
Treatment:
Behavioral: Back School
Control group
No Intervention group
Description:
I declare that I will not change my lifestyle during the study process.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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