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

May 28, 2014 updated by: Lars-Olov Lundqvist, Centre for Rehabilitation Research, Örebro
The purpose of this study is to determine whether sensomotoric training can reduce neck/scapular pain in people with visual disability.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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.

Study Type

Interventional

Enrollment (Actual)

52

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Orebro County
      • Orebro, Orebro County, Sweden, 70212
        • Hälsobro

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 67 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Untreated control
Experimental: Sensomotoric training
Treatment with Sensomotoric 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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
baseline and 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
baseline and 12 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Lars-Olov Lundqvist, Associate Professor, Centre for Rehabilitation Research

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2010

Primary Completion (Actual)

January 1, 2012

Study Completion (Actual)

February 1, 2012

Study Registration Dates

First Submitted

May 25, 2011

First Submitted That Met QC Criteria

May 26, 2011

First Posted (Estimate)

May 27, 2011

Study Record Updates

Last Update Posted (Estimate)

May 29, 2014

Last Update Submitted That Met QC Criteria

May 28, 2014

Last Verified

May 1, 2014

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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