Ignite Creation Date:
2024-05-06 @ 7:24 PM
Last Modification Date:
2024-10-26 @ 3:06 PM
Study NCT ID:
NCT06003907
Status:
COMPLETED
Last Update Posted:
2023-12-07
First Post:
2023-08-15
Brief Title:
Comparison of Conservative Treatment and Graston and Cup Applications in Patients With Cervical Disc Herniation
Sponsor:
Uskudar University
Organization:
Uskudar University
Study Overview
Official Title:
Effectiveness of Graston and Cupping Applications in Individuals With Cervical Disc Herniation A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2024-10
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:
The aim of the study is to examine the effects of graston and dry cupping techniques applied in addition to the conservative treatment program on neck awareness grip strength balance and sleep quality in patients with cervical disc herniation between the ages of 18-65
Detailed Description:
The research will be carried out on 30 cases diagnosed with cervical disc herniation between the ages of 18-65 The patients will be divided into 2 groups as control and experimental groups by simple randomization method While the conservative physical therapy program is applied to the control group the patients in the experimental group will be applied 1 day graston and 1 day dry cup technique in addition to the ones in the experimental group All patients will be treated for 20 sessions 5 days 4 weeks Fremantle Neck Awareness Questionnaire to assess neck awareness hand dynamometer to assess grip strength Berg Balance Scale to assess balance and Jenkins Sleep Scale to assess sleep quality will be used All tests will be measured at the start of treatment and after 4 weeks of intervention Pre- and post-intervention data were statistically analyzed and compared
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