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Completed

NCT Number: NCT01361906

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

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

Completed

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Key information

Conditions

Age range

18 year–67 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Hälsobro

Örebro, Örebro County, 70212, Sweden

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Sensomotoric training

Behavioral

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.

Primary outcomes

  1. Change from Baseline in neck/scapular pain at 12 month

    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.

Secondary outcomes

  1. Change from Baseline in sick leave at 12 month

    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

Sponsors and collaborators

Lead sponsor

Centre for Rehabilitation Research, Örebro

Other Gov

Collaborators

  • University of Gavle
  • Örebro County Council

Registry information

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
May 27, 2011
Registry last updated
May 29, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.