NCT05616611

High-Intensity Laser Therapy Versus Shockwave Therapy in Osteoporotic Long Term Hemiparetic Patients

High-Intensity Laser Therapy Versus Shockwave Therapy on Selected Outcome Measures in Osteoporotic Long Term Hemiparetic Patients: A Randomized Control Trial
Beni-Suef University·ClinicalTrials.gov·radiationCompleted
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Study focus
Disease/Condition
Osteoporosis Secondary
Drug/Device/Intervention
High-Intensity laser
Study type
Interventional
Intervention type
radiation
Sponsor & location
Primary sponsor
Beni-Suef University
Location
Banī Suwayf, Egypt
Timeline & enrollment
Phase
N/A
Start date
Oct 01, 2021
End date
Mar 01, 2022
Enrollment
120 participants
Primary outcome

Quality of Life Questionnaire of the European Foundation for Osteoporosis (QUALEFFO-41),Pain intensity,fall risk assessment

Summary

Background: The relationship between immobilization and localized osteoporosis is well
 documented in chronic stroke patients. Hemiparetic patients are predisposed to fractures and
 usual activity impairment due to a considerable loss of bone density. A serious health care
 challenge is finding ways to reduce osteoporosis and associated fractures among stroke
 survivors. This study aimed to compare the effects of HILT and ESWT in treating osteoporosis
 and its consequences in hemiparetic patients.
 
 Patients and Methods: A randomized controlled trial was performed at the Faculty of Physical
 Therapy Outpatient Clinic, Cairo University. One hundred and twenty hemiplegic patients with
 osteoporosis of both sexes were chosen randomly. They were randomly classified into three
 equal groups (n=40 in each group). The control group received medication and traditional
 physiotherapy programs for stroke patients (strengthening, stretching, and balance exercise).
 The high-intensity laser (HIL) group received the same intervention as the control group in
 addition to high-intensity laser therapy. The shock wave (SW) group received the same
 intervention as the control group in addition to shock wave therapy. The three groups
 received an intervention that lasted 3 sessions/week for 12 weeks). All groups were assessed
 before and after therapy (3 months) for the degree of pain, which was evaluated by visual
 analog scale (VAS), fall risk assessment (overall stability index and Short Form of Berg
 Balance Scale (SFBBS)), and Quality of Life Questionnaire of the European Foundation for
 Osteoporosis (QUALEFFO-41).

ICD-10 classifications
Other osteoporosisOsteoporosis, unspecifiedIdiopathic osteoporosisOsteoporosis in diseases classified elsewhereOsteoporosis in other diseases classified elsewhere
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05616611
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05616611 through Pure Global AI's free database. This phase not specified trial is sponsored by Beni-Suef University and is currently Completed. The study focuses on Osteoporosis Secondary. Target enrollment is 120 participants.

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