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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03608488
Other study ID # Tugbaozsoy
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 6, 2018
Est. completion date July 12, 2019

Study information

Verified date June 2020
Source Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In recent years, skeletal and nonskeletal effects of vitamin D has been studied. One of the effects of it was balance and fall prevention. However, these studies were performed on older patients who had not vitamin D deficiency. This study aimed to evaluate the effect of vitamin D replacement therapy and exercise on balance in 50-70 years-old postmenopausal women.


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date July 12, 2019
Est. primary completion date July 12, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- 50-70 years-old postmenopausal women

- Vitamin D level<10 ng/ml and Vitamin D level>30 ng/ml

- Independant in daily life

- Able to do exercise

- Able to read and write in Turkish

Exclusion Criteria:

- Diabetes mellitus,

- Polyneuropathy,

- Spinal stenosis,

- History of fracture or lower extremity operation,

- Rheumatologic diseases,

- History of chemotherapy

- Cognitive impairment

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Vitamin D
Vitamin D3 50.000 IU/per week, for 8 weeks
Other:
Exercise
Core stability, balance exercises

Locations

Country Name City State
Turkey Sultan Abdulhamid Han Training and Research Hospital Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postural Stability Test (Biodex) Assessed at Baseline overall stability index: quantifying the ability to maintain dynamic postural stability The patient's score on this test assesses deviations from center, thus lower index means less instability and better balance.
Measures were obtained from 20-sec trials during which participants were asked to maintain an upright standing position on their dominant limb on the unstable surface of the Biodex Stability and Balance System.
0 is the minimum score, but there is no defined maximum score
Baseline
Primary Postural Stability Test (Biodex) Assessed After Treatment (8 Weeks) overall stability index: quantifying the ability to maintain dynamic postural stability.
The patient's score on this test assesses deviations from center, thus a lower score is more desirable than a higher score.
Measures were obtained from 20-sec trials during which participants were asked to maintain an upright standing position on their dominant limb on the unstable surface of the Biodex Stability and Balance System 0 is the minimum score, but there is no defined maximum score
After treatment (8 weeks)
Primary Berg Balance Test Assessed at Baseline 14-item scale designed to measure balance of the older adult in a clinical setting minimum: 0 maximum: 56 A score of 56 indicates functional balance. A score of < 45 indicates individuals may be at greater risk of falling. Baseline
Primary Berg Balance Test Assessed After Treatment (8weeks) 14-item scale designed to measure balance of the older adult in a clinical setting minimum: 0 maximum: 56 A score of 56 indicates functional balance. A score of < 45 indicates individuals may be at greater risk of falling. After treatment (8 weeks)
Secondary Fall Risk Assesment Performed at Baseline Biodex fall risk screening test: Patients were instructed to maintain the vertical projection with their center of gravity in the midpoint of the platform 0 is the best possible value, higher score reflects increased risk of falling. But there is no defined maximum score Baseline
Secondary Fall Risk Assesment Performed After Treatment (8 Weeks) Biodex fall risk screening test: Patients were instructed to maintain the vertical projection with their center of gravity in the midpoint of the platform 0° is the best possible value, higher score reflects increased risk of falling. But there is no defined maximum score. After treatment (8 weeks)
Secondary Health Status Assessed at Baseline Notthingham Health Profile: general patient reported outcome measure which measures subjective health status.
38 questions in 6 subareas, with each question assigned a weighted value; the sum of all weighted valuesin a given subarea adds up to 100. Overall score is calculated by summing up 6 subdomian scores.
Ovearall minimum: 0 maximum: 600 (6X100) Higher scores reflect worse health status
Baseline
Secondary Health Status Assessed After Treatment (8 Weeks) Notthingham Health Profile: general patient reported outcome measure which measures subjective health status.
38 questions in 6 subareas, with each question assigned a weighted value; the sum of all weighted valuesin a given subarea adds up to 100. Overall score is calculated by summing up 6 subdomian scores.
Ovearall minimum: 0 maximum: 600 (6X100) Higher scores reflect worse health status.
After treatment (8 weeks)
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