Skip to content

Preventive Program for Work-Related Musculoskeletal Disorders

Influence of a Preventive Program (Educational and Gymnastics) for Work-Related Musculoskeletal Disorders in Surgeons

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02552680
Enrollment
54
Registered
2015-09-17
Start date
2010-10-31
Completion date
2015-08-31
Last updated
2016-07-11

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

Conditions

Quality of Life

Keywords

Work-Related Musculoskeletal Disorders, Quality of life, Health Education

Brief summary

Introduction: Work-Related Musculoskeletal Disorders (WMSDs) are characterized by inflammation of muscles, tendons, fascia and nerves of upper limbs, shoulder girdle and neck. Its incidence is increasing and there is evidence of its association with the pace of work. As WMSDs, another major public health problem is back pain, which also negatively influence the quality of life of patients. These diseases affect many workers, among them, workers in the health area, including surgeons. Studies show that many surgeons are suffering from fatigue and musculoskeletal pain after undergoing surgery, especially laparoscopy. Regarding the quality of life of doctors, a study indicates that surgeons have commitment of domains Vitality and Pain. For these reasons it is important to develop strategies for prevention of occupational risks (WMSDs) in this class of workers. Objectives: To evaluate the influence of a Preventive Program (educational and gymnastics) for prevention of WMSDs, in the quality of life, in limitation of the work, in intensity and frequency of musculoskeletal pain in surgeons of the Hospital de Clínicas de Porto Alegre. There will also be evaluated the effects of the program on muscular strength and flexibility of medics participating in the Preventive Program. Methodology: Randomized clinical trial with a sample of 54 surgeons, divided into two groups: A (Intervention: will participate in eight meetings consisting of exercise and guidelines on care and prevention of WMSDs in activities of daily living, especially those relating work activities) and B (Control: will receive a manual-brochure - containing information about general health). Participants will sign a Letter of Consent.

Detailed description

Clinical Trial Study with 54 surgeons allocated in two groups: A and B. They received two protocols in accordance with the groups they have been allocated. Group A: participated in eight meetings supervised by physical education professionals, with 15 minutes duration, individually administered, twice a week, during the surgeons working hours, at times and places combined with them. The meetings were composed of endurance exercise, mobility and muscle stretching. They were also given guidance on care and prevention of Work-Related Musculoskeletal Disorders in activities fo daily life, especially those related to work activities. Group B: received a manual (brochure ) containing information on general health care, especially designed for this study. With food guide, sleep, physical activity and smoking. Were measured the quality of life, muscle force, muscle stretching and pain. The dates were collected at the beginning of the procedures, 4 weeks after the protocols and 26 after the protocols.

Interventions

OTHERExercise

Physical Exercise

Guideline on care and prevention of Work-Related Musculoskeletal Disorders in activities of daily living, especially those relating work activities.

OTHERBrochure

Manual/brochure containing information about general health

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* surgeons (teachers, contractors and medical residents) * of the Hospital de Clínicas de Porto Alegre * members of General Surgery teams, Digestive Surgery , Plastic Surgery and Coloproctology * of both sexes

Exclusion criteria

* individuals who did not agree to participate in the study * those who were not present at the time of the study (regardless of reason) * those who had some more serious illness that prevented the achievement of study protocols

Design outcomes

Primary

MeasureTime frameDescription
Quality of life26 weeks after the interventionsQuality of life evaluated by the Short-Form Survey Questionnaire (SF-36). Unit of measure: Scale of Quality of life.

Secondary

MeasureTime frameDescription
Muscle strength - Grip and Pinch Strength4 weeks and 26 weeks after the interventionsEvaluated by hand grip dynamometer and pinch grip dynamometer. Unit of measure: kilogram force (kgf) (both evaluations).
Muscle flexibility4 weeks and 26 weeks after the interventionsEvaluated by Banco de Wells. Unit of measure: centimeters (cm)
Musculoskeletal intensity of pain4 weeks and 26 weeks after the interventionsEvaluated by Questionnaire. Unit of measure: Scale of pain.
Quality of life - after 4 weeks4 weeks after the interventionsQuality of life evaluated by the Short-Form Survey Questionnaire (SF-36). Unit of measure: Scale of Quality of life.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026