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Efficacy of Balance Training in Patients With Rotator Cuff Disease

D

Dokuz Eylül University (DEU)

Status

Completed

Conditions

Rotator Cuff Injury

Treatments

Other: Rehabilitation program
Other: Rehabilitation and balance training

Study type

Interventional

Funder types

Other

Identifiers

NCT03054129
2110-GOA

Details and patient eligibility

About

The purpose of the study is to determine whether balance training is effective in patients with rotator cuff disease.

Enrollment

42 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Verification of the diagnosis of rotator cuff disease by a medical practitioner via radiological techniques.
  • Pain due to unilateral rotator cuff disease at least four weeks.

Exclusion criteria

  • Systemic pathology including inflammatory joint disease.
  • More than %50 restriction of passive range of motion in two or more planes.
  • History of major surgery on the lower extremities and shoulder regions.
  • Acute or chronic pain in the spine or lower extremities.
  • An injury of the lower extremities during the last six months which affected functional capabilities.
  • Any kind of neurological complaint.
  • Cardiovascular diseases which affect balance.
  • Acute dizziness
  • Medications which affected balance
  • Subjects who performed balance training

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

42 participants in 2 patient groups

Rehabilitation and balance training
Experimental group
Description:
Each patient will attend rehabilitation program for three days per week for six weeks. Patients will receive balance training in addition to supervised rehabilitation program which is including patient education, stretching and strengthening exercises. Patients will also implement home exercise program. Balance training will be non-supervised program.
Treatment:
Other: Rehabilitation and balance training
Rehabilitation program
Active Comparator group
Description:
Each patient will attend rehabilitation program for three days per week for six weeks. Patients will receive supervised rehabilitation program which is including patient education, stretching and strengthening exercises. Patients will also implement home exercise program.
Treatment:
Other: Rehabilitation program

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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