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Validation of an exercise protocol with a specific instrument for cervical muscle strength gain in individuals with neck pain

Validation of an exercise protocol with a specific instrument for acquiring cervical muscle strength in individuals with neck pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10rc68s9
Enrollment
Unknown
Registered
2025-09-26
Start date
2025-03-03
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Neck pain

Interventions

This is an experimental, longitudinal, quantitative, randomized study to verify the effectiveness of a proposed treatment protocol for neck pain. The sample studied consists of 20 people aged between
cervical muscle strength
resistance of the neck flexor and extensor muscles
activation and isometric resistance of the deep flexors of the cervical spine
and cervical position sense. Participants were randomized through a website (https://www.random.org/) using a random draw. Volunteers were divided into two groups: intervention group and control group
E01.370.600.425

Sponsors

Universidade Federal do Triângulo Mineiro
Lead Sponsor
Universidade Federal do Triângulo Mineiro
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Insidious pain for more than 3 months; average pain intensity of 1 to 5 on the numerical scale; score greater than or equal to 10 and less than 60% on the NDI (Neck Disability Index); people aged between 18 and 65 years; women or men (no gender restriction)

Exclusion criteria

Exclusion criteria: Previous history of neck trauma or surgery; neck pain lasting less than 3 months; oncological and infectious pathologies of the spine; vestibular pathology; complaints of dizziness and tinnitus; individuals undergoing treatment for shoulder dysfunction; occurrence of any musculoskeletal trauma during the study period; withdrawal of the Informed Consent Form and worsening of neck pain

Design outcomes

Primary

MeasureTime frame
It is expected that, through a systematic and evidence-based approach, this protocol may improve the muscle strength of participants with cervical pain

Secondary

MeasureTime frame
It is still expected that this protocol can improve functionality, reduce pain intensity, and increase the range of motion of the participants

Countries

Brazil

Contacts

Public ContactCamilla Peres Almeida

Universidade Federal do Triângulo Mineiro

d202110786@uftm.edu.br+5534999221875

Outcome results

None listed

Source: REBEC (via WHO ICTRP)