Ignite Creation Date:
2024-05-06 @ 8:08 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06264401
Status:
COMPLETED
Last Update Posted:
2024-06-26
First Post:
2024-02-09
Brief Title:
Treatment Exercises With Core Stability and Dynamic Resistance Exercise for Postmenopausal Women With Osteoporosis
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Treatment Exercises With Core Stability and Dynamic Resistance Exercise for Postmenopausal Women With Osteoporosis A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
osteoporosis is a common disease that affect most of postmenopausal women various treatment procedures are used to avoid future complain among postmenopausal population
Detailed Description:
Ethics statement This study was approved by the institutional review board of the faculty of physical therapy Cairo university Egypt noPT REC012003867 and strictly adhered to the criteria proclaimed in the latest version of the declaration of Helsinki code of ethics each woman freely consents to participate in this research study
study design A prospective double-masked randomized controlled trial
sample size calculation Based on a pilot study sample size was calculated according to the significant difference in the value of mean difference pretreatments - posttreatment values of ODI between control 1660 222 and study 2650 409 groups in two tailed unpaired t test with α005 power of 80 and an effect size of 074 So a sample size of 30 patientsper group would be required and increased to 35 women to allow for a 15 dropout rate Power 301 http wwwpsychouni-duesseldorfde Randomization Randomization of sample selection were achieved using closed envelop way to allocate study participants to either intervention group medication and treatment exercises control group medication only all postmenopausal women and examiners were unaware of group allocation
study design A prospective double-masked randomized controlled trial
sample size calculation Based on a pilot study sample size was calculated according to the significant difference in the value of mean difference pretreatments - posttreatment values of ODI between control 1660 222 and study 2650 409 groups in two tailed unpaired t test with α005 power of 80 and an effect size of 074 So a sample size of 30 patientsper group would be required and increased to 35 women to allow for a 15 dropout rate Power 301 http wwwpsychouni-duesseldorfde Randomization Randomization of sample selection were achieved using closed envelop way to allocate study participants to either intervention group medication and treatment exercises control group medication only all postmenopausal women and examiners were unaware of group allocation
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None