- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04898218
Effect of Osteoanabolic Exercises on Gait, Balance & Fear of Fall Among Osteoporotic Females
With the increase in life expectancy women spend more than one-third of their life time in post-menopausal state leading to osteoporosis in later stages. Therefore a decrease in temporal-spatial parameters of gait, high risk of fracture, imbalance in functional parameters, fear of fall and compromised health-related quality of life is observed among osteoporotic females. Several physical activities and balance training programs have been implemented globally but nationally no program has yet been designed catering gait balance and fear of fall altogether as a combined program. Therefore, the aim of this study was to determine the effectiveness of Osteoanabolic exercises on Temporal-Spatial gait parameters, Gait Stability Ratio (GSR) and Bone Mineral Density (BMD) among the osteoporotic females. Moreover, the effectiveness of these exercises was evaluated on dynamic balance using Timed Up and Go Test (TUG).
Furthermore, the impact on fear of fall was identified using Fall Efficacy ScaleInternational (FES-I).
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Karachi, Pakistan, 74700
- Ziauddin University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Postmenopausal osteoporotic females aged in between 50-75 years
- Not participating in any exercise program for the past 3 months
- Independently ambulatory were included in the study
Exclusion Criteria:
• Red flags that limit the recruitment of participants in an exercise program, for example, vertebral fracture, an unstable heart condition, malignancy
Study Plan
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 |
|---|---|
|
Active Comparator: Group A (Aerobic Exercise Group)
Warm-up exercises were performed by the participants on a cycle ergometer for a duration of 5-10 minutes.
Group A was advised to start walking at a comfortable speed on a treadmill for the duration of 30-60 minutes; the intensity of the exercises was 55-75% of MHR, calculated by using a Karvonen method.
Initially with the minimum intensity that was gradually raised up to the intensity of Targeted Heart Rate (THR).
Once the THR is achieved the intensity was gradually decelerated and patient proceeded for the cool-down phase for 5-10 min.
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The exercises were performed for 12 weeks, for the maximum of 6 days/week for Osteoanabolic group, 5 days/week for aerobic group and 3 days/ week for a resistance group as per ACSM, FITT protocol.
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Active Comparator: Group B (Resistance Exercise Group)
Group B was instructed for strengthening exercises of ten major muscle groups that include Biceps, Triceps, Pectoralis Major, Deltoid, Latissimus Dorsi, Abdominals, Back Extensors, Hamstrings, Quadriceps and Calf.
The intensity of the weight-bearing exercises was calculated using 1 Repetition Maximum (RM) method.
|
The exercises were performed for 12 weeks, for the maximum of 6 days/week for Osteoanabolic group, 5 days/week for aerobic group and 3 days/ week for a resistance group as per ACSM, FITT protocol.
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Experimental: Group C (Osteoanabolic Exercise Group)
Group C was performed Osteoanabolic exercise divided into two different phases: Aerobic Conditioning Phase Participants were instructed to walk on treadmill for 30-60 min. The intensity of the exercises was 55-75% MHR, calculated by Karvonen method. Intensity gradually raised up to the Targeted Heart Rate (THR). Once the THR is achieved the intensity was gradually decelerated and patient proceeded for the cool-down phase. The participants performed 3 days per week for 12 weeks on alternative days. Anaerobic (Resistance) Conditioning Phase Resistance training was started on every alternative day of the aerobic conditioning (3 days per week) for 45 min. The intensity of the weight-bearing exercises was calculated using 1 RM method. Resistance training muscle and protocol was the same as for Group B. The participants performed warm-up and cool down similar to that of group A and group B. |
The exercises were performed for 12 weeks, for the maximum of 6 days/week for Osteoanabolic group, 5 days/week for aerobic group and 3 days/ week for a resistance group as per ACSM, FITT protocol.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gait Velocity
Time Frame: Baseline
|
Temporal Spatial Gait Parameter
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Baseline
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Gait Velocity
Time Frame: 12 weeks
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Temporal Spatial Gait Parameter
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12 weeks
|
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Cadence
Time Frame: Baseline
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Temporal Spatial Gait Parameter
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Baseline
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Cadence
Time Frame: 12 weeks
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Temporal Spatial Gait Parameter
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12 weeks
|
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Gait Stability Ratio
Time Frame: Baseline
|
Temporal Spatial Gait Parameter
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Baseline
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Gait Stability Ratio
Time Frame: 12 weeks
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Temporal Spatial Gait Parameter
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12 weeks
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Balance
Time Frame: Baseline
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Balance was measured through Timed-up and Go Test
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Baseline
|
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Balance
Time Frame: 12 weeks
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Balance was measured through Timed-up and Go Test
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12 weeks
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Fear of Fall
Time Frame: Baseline
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Measured through Fall Efficacy Scale- International consisting of 16 items that are summed to calculate a total score from minimum 16 to maximum 64.
Higher the score, greater the fear of falling.
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Baseline
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Fear of Fall
Time Frame: 12 weeks
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Measured through Fall Efficacy Scale- International consisting of 16 items that are summed to calculate a total score from minimum 16 to maximum 64.
Higher the score, greater the fear of falling.
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12 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Bone Mineral Density
Time Frame: Baseline
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Measured through Peripheral DXA Scan on right side calcaneal bone
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Baseline
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Bone Mineral Density
Time Frame: 12 weeks
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Measured through Peripheral DXA Scan on right side calcaneal bone
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12 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amna Khan, Ziauddin University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Amna Khan
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.
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