Skip to content

Effects of Sensomotoric Training on Neck/Scapular Pain in People With Visual Disability

Effects of Sensomotoric Training on Neck/Scapular Pain in People With Visual Disability

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01361906
Enrollment
52
Registered
2011-05-27
Start date
2010-09-30
Completion date
2012-02-29
Last updated
2014-05-29

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

Conditions

Neck/Scapular Pain

Keywords

Musculoskeletal and Neural Physiological Phenomena, Postural Balance, Eye/hand coordination

Brief summary

The purpose of this study is to determine whether sensomotoric training can reduce neck/scapular pain in people with visual disability.

Detailed description

People with prolonged musculoskeletal disorders have impaired quality of life, physical function, work conditions and work ability and consume substantial public resources. An often overlooked fact in this context is the relationship between musculoskeletal disorders and the importance of a normally functioning visual system. People who have a visual impairment in adulthood often experience reduced health and life satisfaction. Many people lose their faith in order to continue with the activities previously carried out as to cope with their life, their work, and in some cases,personal care. Rehabilitative efforts to reduce the negative effects often involve the prescription of various visual aids which, in turn, often leads to unfavourable ergonomic and static postures with further increased risk of musculoskeletal problems. A prevention of such disorders is likely to allow them to continue their work, which is important from both an individual and a society perspective. The overall objective of the project is to evaluate the effects of an intervention program and develop a theoretical model for the relationship between near work, eye disorders and musculoskeletal disorders. The intervention is to be evaluated in a randomized trial on people with impaired vision and pain in the neck and scapular area. An intervention based on development and adaptation of an established physiotherapy practice in order to increase body awareness, body control and movement patterns will be evaluated. The effects of the intervention will be measured by a variety of outcome measures derived from WHO's ICF-model. An innovative solution for establishing proprioception and eye-hand coordination in everyday activities, the Clinical Kinematic Assessment Tool, will be used.

Interventions

BEHAVIORALSensomotoric training

The intervention will be given once a week (2h per occasion) for twelve weeks. Each occasion is planned to have the following structure: 10 min initial conversation about how participants are feeling today and how it felt after the last time. 70 min guided sensory motor learning. 10 min final talks, reflections on how it felt today.

Sponsors

Örebro County Council
CollaboratorOTHER_GOV
University of Gavle
CollaboratorOTHER
Centre for Rehabilitation Research, Örebro
Lead SponsorOTHER_GOV

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 67 Years
Healthy volunteers
No

Inclusion criteria

* visual disability * age 18 to 67 years old * pain in neck/scapular area * living in Örebro county

Exclusion criteria

* deafness * musculoskeletal disease (such as Multiple sclerosis, etc)

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in neck/scapular pain at 12 monthbaseline and 12 monthsPhysiotherapeut palpation of left and right M.Trapezius, M.Occiput, and M.Levator scapulae. Patient rate degree of pain on 100 mm VAS.

Secondary

MeasureTime frameDescription
Change from Baseline in sick leave at 12 monthbaseline and 12 monthPatient self reported sick leave and sickleave registered at persons employer (if any) and/or at the Swedish Social Insurance Agency

Countries

Sweden

Outcome results

None listed

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