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Clinical Trials/NCT05889104
NCT05889104
Completed
Not Applicable

The Effect of Progressive Loading Protocol on Bone Mineral Density and Quality of Life in Osteoporotic Patients.

Imam Abdulrahman Bin Faisal University1 site in 1 country92 target enrollmentJune 1, 2023
ConditionsOsteoporosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoporosis
Sponsor
Imam Abdulrahman Bin Faisal University
Enrollment
92
Locations
1
Primary Endpoint
Measuring the result of change by Dual energy x ray absorptiometry (DXA) During the Intervention
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aims of this study are to examine the effects of Progressive Loading Exercises Protocol on Bone Mineral Density in osteoporotic patient's well-being and quality of life before a fracture occurs in order to create remedies. In addition, the available data from health research and clinical studies on osteoporosis will be evaluated for their impact on patient well-being and quality of life, providing an up-to-date and comprehensive overview of evidence-based treatments.

Detailed Description

Progressive Loading Protocol (PLP): The subjects in the Progressive Loading Group will undergo 4-7 days of moderate to high impact loading activities per week for the duration of 6 weeks. The PLP is adapted and modified based on Exercise and Sports Science Australia (ESSA) position statement on exercise prescription for the prevention and management of Osteoporosis. The participants in the progressive loading group will perform vertical and multidirectional jumping, bounding, hopping, skipping rope, drop jumps and bench stepping. The weight bearing intensity will be progressed by increasing heights for activities such as bounding and drop jumping, adding weighted vests and changing directions. To prevent the risk of injury, the participants would be instructed to avoid the loaded spine flexion or twisting movements of the spine. Frail individuals should be supervised and exercised within reach of a railing or other stable support. Intensity: Moderate-to-high weight bearing impact loads (\>2 times body weight) that are progressive, novel, and multidirectional, within the limits of pain, increasing as tolerated. Frequency: 4-7 days per week Sets/Repetitions: Aim to work up to 50 repetitions over time (5 sets of 10 repetitions with 1-2 min rest between sets) The subjects in the Control Group will undergo twelve weeks of low impact Aerobics Training along with a health awareness program..

Registry
clinicaltrials.gov
Start Date
June 1, 2023
End Date
August 5, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Saeed Mufleh

Senior Physiotherapist

Imam Abdulrahman Bin Faisal University

Eligibility Criteria

Inclusion Criteria

  • Subject with history of diabetes, hypertension

Exclusion Criteria

  • Subject with history of kidney diseases, cardiopulmonary diseases, thrombosis, hyperprolactinemia, spondylolisthesis, back/leg deformities or surgeries, osteoarthritis, pacemakers, implants of the lower extremity and spine, tumors, migraines, or having any other diseases that affect bone metabolism or neuromuscular performance.

Outcomes

Primary Outcomes

Measuring the result of change by Dual energy x ray absorptiometry (DXA) During the Intervention

Time Frame: At the start of the intervention, then the measurement is done again after six weeks..

to measure bone mineral density (BMD) at the spine and hip region. and hip regio

Study Sites (1)

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