Ignite Creation Date:
2024-05-06 @ 3:52 PM
Last Modification Date:
2024-10-26 @ 1:59 PM
Study NCT ID:
NCT04789265
Status:
COMPLETED
Last Update Posted:
2021-05-26
First Post:
2021-03-02
Brief Title:
Instrumental Soft Tissue Mobilization in Patients With Chronic Neck Pain
Sponsor:
Ayşegül BOSTAN
Organization:
Medipol University
Study Overview
Official Title:
Instrumental Soft Tissue Mobilization in Patients With Chronic Neck Pain a Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2021-05
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:
In this study it was planned to investigate the effectiveness of instrument-assisted soft tissue mobilisation IASTM in patients with chronic neck pain Forty eight individuals with chronic neck pain between the ages of 18-70 were included in the study Individuals were randomly divided into two groups as Combined Therapy CT n 24 and Exercise Therapy ET n 24 groups All exercises were applied to the participants for 4 weeks 3 times a week by an experienced physiotherapist for 5 years under supervision ET which included stretching and strengthening exercises involving the neck shoulder and around the scapula muscles applied according to the tolerance of the individuals and targeted to be most beneficial in daily life activities
CT in addition to the ET applied 3 times a week for 4 weeks the participants received a total of 8 sessions of IASTM on the days they came to the treatment twice a week before the ET As soon as the participants came to the session IASTM was applied first Following the IASTM application ET was applied in the same protocol and under the same therapist supervise with the ET group
Before and after treatment deep neck flexor muscle endurance DNFME pain severity with Visual Analogue Scale VAS and Brief Pain Inventory BPI functional status with Neck Disability Index NDI quality of life with Nottingham Health Profile NHP treatment and treatment satisfaction was evaluated
CT in addition to the ET applied 3 times a week for 4 weeks the participants received a total of 8 sessions of IASTM on the days they came to the treatment twice a week before the ET As soon as the participants came to the session IASTM was applied first Following the IASTM application ET was applied in the same protocol and under the same therapist supervise with the ET group
Before and after treatment deep neck flexor muscle endurance DNFME pain severity with Visual Analogue Scale VAS and Brief Pain Inventory BPI functional status with Neck Disability Index NDI quality of life with Nottingham Health Profile NHP treatment and treatment satisfaction was evaluated
Detailed Description:
None
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