- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03882853
The Effect of Yoga Asana 'Vrksasana (Tree Pose)' on Balance in the Patients With Osteoporosis
Patients with T score of bone mineral densitometry less than or equal to -2.5 will be included in the study. Initial evaluation consists of obtaining demographic data, performing international physical activity questionnaire (short form) Additionally; Berg balance test, timed sit and walk test, single leg stance test, tandem walk test, tandem stance test will be performed. Baseline static and dynamic balance scores of patients will be determined by the Corebalance Premiere-19 balance device. After acclimation the device and tests, 3 measurements will be made and the most successful score will be taken. The lowest value will be showing best performance. After the first evaluation, patients will be randomized using windows excel randomization option to two groups by another observer. Patients will be blinded about which exercise group they will be separated to. Both groups will be thought exercise series which will be based on recommendations which is published on October 2016 by UK national osteoporosis foundation. Patients would be encouraged to perform the exercises on recommended basis and handouts will be given to patients in both groups. The yoga group will also be taught "tree pose".
Patients will be encouraged to note their exercises regularly on daily basis. Patients will be reevaluated after first and third months and balance tests will be re-performed to determine the effect of given exercises.
Exclusion criteria
- Neurological or vestibule dysfunctions which may affect balance
- Severe mental disturbances effecting communication
- Locomotor dysfunction which prevents patient to perform balance tests
- Active musculoskeletal pathology which disrupt performing exercises.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patients with osteoporosis who applied to PMR outpatient clinic of Istanbul Medeniyet University Goztepe Training and Research Hospital will be included in the study. Informed consent detailing the purpose and content of the study will be obtained from patients. Initial evaluation of patients will be performed by the same doctor. Initial evaluation consists of obtaining demographic data and performing international physical activity questionnaire (short form) to evaluate physical activity frequencies of patients. Additionally; Berg balance test, timed sit and walk test, single leg stance test, tandem walk test, tandem stance test will be performed. Baseline static and dynamic balance scores of patients will be determined by the Corebalance Premiere-19 balance device. After acclimation the device and tests, 3 measurements will be made and the most successful score will be taken. The lowest value will be showing best performance. After the first evaluation, patients will be randomized using windows excel randomization option to two groups by another observer. Patients will be blinded about which exercise group they will be separated to. To learn the exercises the patient will be referred to physiatrist Ozge Solakoglu who completed a 200-hour yoga teacher training programme certificated by Yoga Alliance. Both groups will be thought exercise series which will be based on recommendations which is published on October 2016 by UK national osteoporosis foundation. Patients would be encouraged to perform the exercises on recommended basis and handouts will be given to patients in both groups. The yoga group will also be taught "tree pose".
Patients will be encouraged to note their exercises regularly on daily basis. Patients will be reevaluated after first and third months and balance tests will be re-performed to determine the effect of given exercises.
Inclusion criteria
- Patients with T score of bone mineral densitometry lower than -2.5.-
Exclusion criteria
- Neurological or vestibule dysfunctions which may affect balance
- Severe mental disturbances effecting communication
- Locomotor dysfunction which prevents patient to perform balance tests
- Active musculoskeletal pathology which disrupt performing exercises.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey, 34732
- Istanbul Medeniyet University Faculty of Medicine, Physical Medicine and Rehabilitation Department
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients with T score of bone mineral densitometry lower than -2.5.
Exclusion Criteria:
- Neurological or vestibule dysfunctions which may affect balance
- Severe mental disturbances effecting communication
- Locomotor dysfunction which prevents patient to perform balance tests
- Active musculoskeletal pathology which disrupt performing exercises.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: Conservative exercise group (CEG)
Conservative exercise group
|
The group will be thought exercise series which based on recommendations published on October 2016 by UK national osteoporosis foundation.Handouts including pictures and narrations of the exercises will be given to patients.
Patients would be encouraged to perform the exercises 5 days a week.
A diary will be given to note the days exercises completed.
Other Names:
|
|
EXPERIMENTAL: Tree pose added exercise group (TPAEG)
Tree pose added exercise group
|
The group will be thought exercise series which based on recommendations published on October 2016 by UK national osteoporosis foundation.Handouts including pictures and narrations of the exercises will be given to patients.
Patients would be encouraged to perform the exercises 5 days a week.
A diary will be given to note the days exercises completed.
Other Names:
The group will be thought exercise series which will be based on recommendations which is published on October 2016 by UK national osteoporosis foundation, also be taught "tree pose" of yoga.
Handouts including pictures and narrations of the exercises will be given to patients.
Patients would be encouraged to perform the exercises 5 days a week.
A diary will be given to note the days exercises completed.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Static balance score
Time Frame: 5 min.
|
The Korebalance Premiere-19 device and software will be used to make balance assessment.
Static test requires standing steady and balancing on the platform, keeping the cross-hairs of cursor in the center of the test pattern.
The score indicates the deviation of user's center of gravity from the center of the pattern.
After familirization of the patient to the test, the lowest score of three measurements will be noted.
The lowest score gives the most successfull scores of test.
|
5 min.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic balance score
Time Frame: 5 min.
|
The Korebalance Premiere-19 device and software will be used to make balance assessment.
Dinamic test offers a moving cursor that the user ''follows''.
Cursor patterns a clock-wise circle.
After familirization of the patient to the test, the lowest score of three measurements will be noted.
The lowest score gives the most successfull scores of test.
|
5 min.
|
|
Berg balance test score
Time Frame: 10 min.
|
14-item scale designed to measure balance of the older adult in a clinical setting.
A five-point ordinal scale, ranging from 0-4. "0" indicates the lowest level of function and "4" the highest level of function.
Total Score is 56.
Score of 41-56 indicates low fall risk, 21-40 indicates medium fall risk, 0 -20 indicates high fall risk.
It is supported a cut off score of 45/56 for independent safe ambulation.
|
10 min.
|
|
Timed sit and walk test score
Time Frame: 1 min.
|
The objective is to determine fall risk and measure the progress of balance, sit to stand and walking.
The patient starts in a seated position, the patient stands up upon command, walks 3 meters, turns around, walks back to the chair and sits down.
The time stops when the patient is seated.
The subject is allowed to use an assistive device.
If an assistive device is used, it will be documented.
|
1 min.
|
|
Single leg stance test score
Time Frame: 1 min
|
It is used to test the static balance and postural control.
It is performed eyes open and arms on the hips.
The patient must stand unassisted on one leg.
The time between one foot is flexed off the floor to the time when it touches the ground.
If less then 30 second, it will be noted, patients stands with more than 30 seconds accepted succesfull.
|
1 min
|
|
Tandem walk test score
Time Frame: 1 min
|
The patient will asked to walk in a straight line with one foot immediately in front of the other (heel to toe) for 10 footstep for each foot.
The time will be documented.
|
1 min
|
|
Tandem stance test score
Time Frame: 1 min
|
The patient will be ask to stand tandem (heel to toe) for 30 seconds.
Lower than 30 second will be documented.
|
1 min
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ozge Solakoglu, MD, Istanbul Medeniyet University Physical Medicine and Rehaiblitation Clinic
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FTR OP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Osteoporosis
-
Radius Health, Inc.CompletedOsteoporosis | Osteoporosis Risk | Osteoporosis, Postmenopausal | Osteoporosis Fracture | Osteoporosis, Age-Related | Osteoporosis Localized to Spine | Osteoporosis Senile | Osteoporosis of Vertebrae | Osteoporosis VertebralUnited States
-
Radius Health, Inc.CompletedOsteoporosis | Age Related Osteoporosis | Osteoporosis, Age-Related | Osteoporosis Localized to Spine | Osteoporosis Senile | Osteoporosis of VertebraeUnited States, Poland, Italy
-
National Taiwan University HospitalRecruitingOsteoporosis | Osteoporosis PostmenopausalTaiwan
-
Hoffmann-La RocheCompletedPostmenopausal OsteoporosisUnited States
-
Hoffmann-La RocheCompletedPost Menopausal OsteoporosisUnited States, Puerto Rico
-
Appalachian State UniversityNorth Carolina Agriculture & Technical State UniversityCompletedPostmenopausal Osteoporosis | Osteoporosis, OsteopeniaUnited States
-
Centre Hospitalier Universitaire de Saint EtienneMinistry of Health, FranceRecruitingPost Menopausal OsteoporosisFrance
-
AmgenCompletedPost Menopausal OsteoporosisFrance
-
Hoffmann-La RocheCompletedPost Menopausal OsteoporosisUnited States
-
Hoffmann-La RocheCompletedPost Menopausal OsteoporosisSpain, South Africa, Germany, Mexico, United States, Canada, France, United Kingdom, Italy, Belgium, Australia, Poland, Denmark, Hungary, Czech Republic, Norway
Clinical Trials on Conservative exercise group
-
Universidad Rey Juan CarlosHospital Universitario Fundación AlcorcónCompleted
-
Ataturk Training and Research HospitalCompleted
-
Riphah International UniversityNot yet recruiting
-
The Hong Kong Polytechnic UniversityUnknownRheumatoid ArthritisHong Kong
-
Michael Wilson & Associates Health Care Consulting...Pneumex CorporationTerminatedLow Back Pain | RadiculopathyUnited States
-
University of PeradeniyaNot yet recruiting
-
Cyprus University of TechnologyCyprus Institute of Neurology and GeneticsCompletedMultiple Sclerosis, Secondary Progressive | Multiple Sclerosis, Primary ProgressiveCyprus
-
Medipol UniversityCompletedLow Back PainTurkey (Türkiye)
-
Riphah International UniversityCompletedCervical Disc HerniationPakistan
-
Ankara Yildirim Beyazıt UniversityUnknownArthroplasty, Replacement, KneeTurkey