Skip to content

Workplace Based Physiotherapy of Elderly-care Workers With Non-specific Neck Pain.

Workplace Based Physiotherapy of Elderly-care Workers With Non-specific Neck Pain: a Five Week Intervention With a One Month Follow-up Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06346249
Enrollment
50
Registered
2024-04-04
Start date
2024-03-04
Completion date
2024-05-31
Last updated
2025-05-01

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

Conditions

Neck Pain

Keywords

non specific pain, physiotherapy, manual therapy, electrical stimulation therapy, therapeutic exercise

Brief summary

The overall objective of this study is to determine the efficacy of a physical therapy intervention based on manual therapy, therapeutic exercise and application of electrotherapy in healthcare workers with non-specific neck pain.

Detailed description

The subjects included in the sample will be evaluated according to the aforementioned parameters by researchers trained and assigned for this purpose. The data collection of the different variables will be performed before and after the completion of the program designed for the study. The physiotherapy intervention for the experimental group will have a duration of 10 sessions, twice a week.

Interventions

Ten Electrical Stimulation Therapy sessions lasting 30 minutes were carried out. Analgesic currents of the TENS type, placed in the cervical region.

OTHERManual Therapy

Manual Therapy consistin of soft tissue mobilization and release techniques over the neck and craniocervical regions. Ten sessions.

The exercise therapeutic program consisting of neck movement control and stretching exercise. Ten sessions.

Sponsors

Universidad de Extremadura
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

IInclusion Criteria: * Age range between 18-60 years. * Cervical pain of non-specific origin or Cervicalgia type I and II according to the Quebec - Task Force on Spinal Disorders. * Be willing to participate in the study and sign the informed consent form. * Have at least one year of seniority in the company exercising the current professional activity within the team of socio-health personnel.

Exclusion criteria

* Cervicalgia with neurological involvement or caused by pathologies such as: inflammatory disease, neurological disease, rheumatic disease, severe osteoporosis, fracture, dislocation, vertebro-basilar insufficiency, neoplasia or infection. * Spine surgery. * Present metallic implants at the spinal column level. * Have received physiotherapy or alternative treatment in the last 6 months before starting the study. * To present any type of inconvenience to the application of electrotherapy (score ≥45 points in EAPP).

Design outcomes

Primary

MeasureTime frameDescription
Changes in Pain5 weeksA visual analog scale (VAS). The scale is represented by a 10-centimeter line at the ends of which there are two adjectives whose ends there are two adjectives, absence of pain (0) and unbearable pain (10). The higher the score, the greater the pain.
Changes Pressure Pain5 weeksPressure Pain with Algometry. To assess the mechanosensitivity of the trigger points , the pain threshold was measured at the pressure. Unit of measure Kg/cm2.
Changes in Disability5 weeksNeck Disability Index ( NDI) through which will give us the degree of disability neck pain.The NDI consists of 10 sections, 4 of them are related to subjective symptoms (pain intensity, headache, head, ability to concentrate and quality of sleep) and the other 6 are related to basic activities of daily living (ABVD) (personal care, ability to lift weights, reading, work, driving, leisure activities and free time). Each of the sections presents 6 possible answers, scoring these from 0 to 5 according to the progression of functional disability.

Secondary

MeasureTime frameDescription
Changes in Range of Motion5 weeksMeasurement of joint amplitude with goniometry. The Range of Motion (ROM) exploration was performed with the subjects in sitting in order to stabilize the pelvis and the thoracic-lumbar spine. From this position, the degrees of maximum position reached by the subjects in each of the 6 movements of space. Unit of measurement in degrees of articulation.
General Health.5 weeksThe Physical and Mental Health summary scales-12 (SF-12) contains 12 questions distributed in each of the 8 dimensions. The higher the score, the better the state of health.

Countries

Spain

Outcome results

None listed

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