Hälsobro
Örebro, Örebro County, 70212, Sweden
NCT Number: NCT01361906
The purpose of this study is to determine whether sensomotoric training can reduce neck/scapular pain in people with visual disability.
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Notify Me18 year–67 year
All sexes
Interventional
Phase 4
Örebro, Örebro County, 70212, Sweden
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: baseline and 12 months
Physiotherapeut palpation of left and right M.Trapezius, M.Occiput, and M.Levator scapulae. Patient rate degree of pain on 100 mm VAS.
Time frame: baseline and 12 month
Patient self reported sick leave and sickleave registered at persons employer (if any) and/or at the Swedish Social Insurance Agency
Centre for Rehabilitation Research, Örebro
Other Gov
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