- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01361906
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
Other Study ID Numbers
- REHSAM/11
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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Clinical Trials on Sensomotoric training
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University of Sao PauloFundação de Amparo à Pesquisa do Estado de São PauloCompletedHypertension | Diabetes | Peripheral Arterial DiseaseBrazil
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Lebanese UniversityCompletedHeart Failure | Quality of Life | Cardiac Rehabilitation | Aerobic Exercise | Exercise Intolerance | Respiratory Muscle Training | Strength Training
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Poznan University of Physical EducationPoznan University of Medical Sciences; National Science Centre, PolandActive, not recruitingHealthy Athletes Aged 18-35 YearsPoland
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Norwegian University of Science and TechnologySt. Olavs HospitalCompletedHyperglycemia | Diabetes Mellitus, Type 2Norway