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Sustained Natural Apophysial Glides (SNAGs) Technique in Non-Specific Neck Pain Patients

Primary Purpose

Neck Pain

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
application of SNAGs technique
Sponsored by
Hacettepe University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neck Pain focused on measuring manual therapy, neck pain, SNAGs, sleep quality, quality of life

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Volunteer patients with non-specific neck pain lasting at least 3 months,
  • Volunteer patients without radicular pressure,
  • Volunteer patients with loss of strength,
  • Volunteer patients diagnosed with non-specific neck pain by a specialist physician.

Exclusion Criteria:

  • Volunteer patients with central nervous system disease,
  • Volunteer patients with distal-peripheral nerve injuries,
  • Volunteer patients with inflammatory joint disease,
  • Volunteer patients with cervical spine fracture or surgery, upper extremity surgery,
  • Volunteer patients with vertebrobasilar artery stenosis,
  • Volunteer patients with osteoporosis,
  • Volunteer patients with cervical dislocation,
  • Volunteer patients with cervical spine tumor and infection,
  • Volunteer patients with congenital anomalies involving the spine,
  • Volunteer patients with patients with diabetes.

Sites / Locations

  • Istınye University Medical Park Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

experiment group

control group

Arm Description

Number of participant is 16. In addition to the conventional therapy, SNAGs technique was applied.

Number of participant is 16. Only the conventional therapy was applied.

Outcomes

Primary Outcome Measures

Range of motion assessments
Active and passive range of motion
Pain assessments
McGill Pain Scale; minimum pain score: 0, maximum pain score: 78, The higher the pain score the greater the pain.

Secondary Outcome Measures

Sleep quality assessments
Pittsburgh Sleep Quality Index (PSQI)
Quality of life assessments
The Nottingham Health Profile

Full Information

First Posted
June 8, 2022
Last Updated
June 15, 2022
Sponsor
Hacettepe University
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1. Study Identification

Unique Protocol Identification Number
NCT05425706
Brief Title
Sustained Natural Apophysial Glides (SNAGs) Technique in Non-Specific Neck Pain Patients
Official Title
Investigation of the Effectiveness of Mulligan Concept Sustained Natural Apophysial Glides (SNAGs) Technique in Non-Specific Neck Pain Patients: A Randomized Controlled Single Blinded Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
April 22, 2019 (Actual)
Primary Completion Date
January 6, 2020 (Actual)
Study Completion Date
April 6, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hacettepe University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Mechanical neck pain is defined for the absence of cervical spinal pathologies.With the SNAGs mobile mobilization method, it reveals effective results in cases of limitation and pain in the cervical joints.Although there are studies with the Mulligan concept in the literature, studies examining the effects of the SNAGs technique on non-specific neck pain are limited. The aim of this study is to investigate the effectiveness of the Mulligan Concept SNAGs mobilization method applied in addition to the conventional physiotherapy program in individuals with nonspecific neck pain.
Detailed Description
This study was conducted to investigate the effectiveness of Mulligan concept cervical sustained natural apophysial glides (SNAGs) mobilization method in addition to the conventional treatment program in patients with nonspecific neck pain. The study included 40 patients (18-50 years of age) with non-specific neck pain, radicular compression and loss of strength for at least 3 months, diagnosed by a specialist physician; patients with central nervous system disease, distal-peripheral nerve injuries Patients with inflammatory joint disease, cervical spine fracture or surgery, patients with upper extremity surgery, cervical spine tumor and infection, cervical spine congenital anomaly and diabetes were not included in the study. 15 sessions were applied for 3 weeks, 5 days a week for 10 weeks, 10 minutes ultrasound, 20 minutes transcutaneous electrical nerve stimulation (TENS) and hotpack application and Mulligan mobilization in addition to physiotherapy programs. The patient was rested for 5 seconds between sets. The physiotherapy program was applied to the control group and the application session was completed. Normal range of motion exercises were performed in both groups and given as home exercise.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Pain
Keywords
manual therapy, neck pain, SNAGs, sleep quality, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
experiment group
Arm Type
Experimental
Arm Description
Number of participant is 16. In addition to the conventional therapy, SNAGs technique was applied.
Arm Title
control group
Arm Type
No Intervention
Arm Description
Number of participant is 16. Only the conventional therapy was applied.
Intervention Type
Other
Intervention Name(s)
application of SNAGs technique
Intervention Description
in experiment group, the SNAGs technique was applied to 16 participants in addition to conventional therapy.
Primary Outcome Measure Information:
Title
Range of motion assessments
Description
Active and passive range of motion
Time Frame
Two weeks for each participants
Title
Pain assessments
Description
McGill Pain Scale; minimum pain score: 0, maximum pain score: 78, The higher the pain score the greater the pain.
Time Frame
Two weeks for each participants
Secondary Outcome Measure Information:
Title
Sleep quality assessments
Description
Pittsburgh Sleep Quality Index (PSQI)
Time Frame
Two weeks for each participants
Title
Quality of life assessments
Description
The Nottingham Health Profile
Time Frame
Two weeks for each participants

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Volunteer patients with non-specific neck pain lasting at least 3 months, Volunteer patients without radicular pressure, Volunteer patients with loss of strength, Volunteer patients diagnosed with non-specific neck pain by a specialist physician. Exclusion Criteria: Volunteer patients with central nervous system disease, Volunteer patients with distal-peripheral nerve injuries, Volunteer patients with inflammatory joint disease, Volunteer patients with cervical spine fracture or surgery, upper extremity surgery, Volunteer patients with vertebrobasilar artery stenosis, Volunteer patients with osteoporosis, Volunteer patients with cervical dislocation, Volunteer patients with cervical spine tumor and infection, Volunteer patients with congenital anomalies involving the spine, Volunteer patients with patients with diabetes.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
DUYGU KORKEM YORULMAZ, PhD.
Organizational Affiliation
ISTINYE UNİVERSITY
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istınye University Medical Park Hospital
City
Istanbul
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25097535
Citation
Ali A, Shakil-Ur-Rehman S, Sibtain F. The efficacy of Sustained Natural Apophyseal Glides with and without Isometric Exercise Training in Non-specific Neck Pain. Pak J Med Sci. 2014 Jul;30(4):872-4.
Results Reference
background
PubMed Identifier
24877050
Citation
Shin EJ, Lee BH. The effect of sustained natural apophyseal glides on headache, duration and cervical function in women with cervicogenic headache. J Exerc Rehabil. 2014 Apr 30;10(2):131-5. doi: 10.12965/jer.140098. eCollection 2014 Apr.
Results Reference
result

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Sustained Natural Apophysial Glides (SNAGs) Technique in Non-Specific Neck Pain Patients

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