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Effectiveness of a Cognitive and Physical Intervention to Reduce Head and Muscle Pain in Working Communities

U

University of Turin

Status and phase

Completed
Phase 3

Conditions

Shoulder Pain
Headache Disorders
Neck Pain
Headache

Treatments

Behavioral: Cognitive, behavioral, exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT00457496
5147SD2003.0271

Details and patient eligibility

About

The primary purpose of this study is to evaluate the effectiveness of a workplace cognitive and physical program (Intervention), in reducing the frequency of head and neck pain

Full description

Many studies have been performed to assess the efficacy of non invasive physical interventions in the treatment of different types of headache and cervical pain. However the evidence on their effectiveness is still limited and the results of recent studies are conflicting.

The primary objective of this study is to evaluate the effectiveness of a workplace cognitive and physical programme (Intervention) in reducing the frequency of pain involving the head and neck area. The Intervention consists of brief shoulder and neck exercises to be performed several times a day, a relaxation exercise and instructions of how to reduce parafunction and hyperfunction of the craniofacial and cervical muscles during the day.

Comparison(s): Group of employees that will receive a cognitive/physical programme (Intervention), compared to a similar group of employees that will not receive the Intervention (Controls); (frequency of headache and neck and shoulder pain).

Enrollment

300 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects employed at the Municipality of Turin ( Registry-Tax office) from the 1th January 2005 that will give informed consent before starting the study.

Exclusion criteria

  • Because of the pragmatic design, no exclusion criteria are required for this study

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 1 patient group

A
Active Comparator group
Treatment:
Behavioral: Cognitive, behavioral, exercise

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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