The Effectiveness of Manipulation Treatment in Cervical Region

Sponsor
Abant Izzet Baysal University (Other)
Overall Status
Completed
CT.gov ID
NCT04455048
Collaborator
(none)
84
2
2
10.6
42
3.9

Study Details

Study Description

Brief Summary

Neck pain is the second most common musculoskeletal pain after lumbar pain. Prevalence is 27.2% female and 17.4% in male population (1, 2). Approximately 1/3 of acute onset neck aches become chronic. It causes increasing the cost of treatment and also the loss of labor (3, 4).

Condition or Disease Intervention/Treatment Phase
  • Other: Cervicothoracic thrust manipulation
  • Other: Cervicothoracic thrust manipulation sham
N/A

Detailed Description

Acute neck pain is often caused by mechanical causes and can be classified as rheumatic diseases, infectious and tumoral pathologies, metabolic bone diseases such as osteoporosis and osteomalacia, pain reflected the cervical region. A-V malformation and syringomyelia are the causes of chronic cervical pain (5). Mechanical neck pain is a non-radicular pain caused by local musculoskeletal structures and is characterized by a spasm of the cervical muscles. (6, 7). Posture, emotional stress, cold and fatigue are etiologic causes, and pain is also reflected in the cervical, occipital and scapular regions depending on the severity of muscle spasm and the presence of trigger point in myofascial pain syndrome (9, 10). Many authors have suggested that facet joints are associated with mechanical dysfunction as a common cause of cervical pain (8-10).

The pain in the head and neck region affects the quality of life, cognitive and functional status of the person. The most important difficulty and failure in the treatment of such pain arise from the inability to diagnose the disease correctly. Good anatomical and biomechanical properties of the region, comprehensive anamnesis, physical examination under static and dynamic conditions, laboratory and radiological examinations are the most important milestones of diagnosis (12). In most cases, medical treatment and physical therapy modalities (superficial and deep heat, electrotherapy, laser, traction, massage, spa) are sufficient for pain relief and recovery of function, but interventional procedures and surgical procedures are needed for the fewer patient. Recently, spinal mobilization and manipulation techniques can be used to relieve pain and restore function in the early stages. Although it is a safe method, in order to prevent the rare complications it is necessary to determine the indications of treatment correctly, to exclude contiguous cases and to apply the manipulation by experts (12).

Study Design

Study Type:
Interventional
Actual Enrollment :
84 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups with a sham control. Assessments will be performed before manipulation, immediately after first session, in the second week, and two months after the last session.Two groups with a sham control. Assessments will be performed before manipulation, immediately after first session, in the second week, and two months after the last session.
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
The manipulation group will receive a single session thrust manipulation and the control group will receive a sham manipulation. Outcome assessment will be performed by another investigator.
Primary Purpose:
Treatment
Official Title:
The Effectiveness of Manipulation Treatment in Acute Cervical Region Pain
Actual Study Start Date :
Jul 2, 2020
Actual Primary Completion Date :
Apr 16, 2021
Actual Study Completion Date :
May 22, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

A single-session manipulation with a high-speed low-amplitude thrust technique in the cervicothoracic transition region will be applied each week for two weeks.

Other: Cervicothoracic thrust manipulation
The patient will be positioned in a supine position with arms crossed over over the trunk and holding the shoulders. The therapist will place a stabilizing hand over transverse process of T1 in pistol grip and contacted patients elbow with sternum and patient will be asked do a hip bridge while taking a deep breath than exhale. Thrust manipulation will be applied at the end of exhale.

Sham Comparator: Control Group

A sham manipulation without a high-speed low-amplitude thrust technique in the cervicothoracic transition region will be applied.

Other: Cervicothoracic thrust manipulation sham
The patient will be positioned in a supine position with arms crossed over over the trunk and holding the shoulders. The therapist will place a stabilizing hand over transverse process of T1 in pistol grip and contacted patients elbow with sternum and patient will be asked do a hip bridge while taking a deep breath than exhale. A soft compression will be applied at the end of exhale without a thrust.

Outcome Measures

Primary Outcome Measures

  1. Pain pressure threshold [two weeks]

    Pain pressure threshold (PPT). was assessed with an analogue algometry (Baseline, FEl Inc. White Plains, NY,USA) with 1 cm2 rubber tip was used to measure the pain pressure threshold. Algometer perpendicularly placed over spinous process of T1 on prone position and pressure progressively increased 1 kg/s until patients verbally reported pain under the tip of algometer or referring pain. Measurement repeated three times and average score recorded.

Secondary Outcome Measures

  1. Visual analog scale [two weeks]

    The patient was asked to mark the severity of his or her pain with active motion on a horizontal line 100 millimeters in length. The intensity of the pain was calculated by measuring the area in which the individual marked between 0 (no pain) and 10 (the most severe pain I felt in my life).

  2. Cervical range of motion [two weeks]

    Cervical Range of Motion (ROM) of flexion,extension, lateral flexion and rotation were measured with basic cervical ROM device (Performance Attainment, Associates, St Paul, MN, USA) in seated position without back support.

  3. Neck Disability Index [two weeks]

    Perceived disability of patients was assessed with 10-item item Neck Disability Index (NDI),which a modified from Oswestry Low Back Pain Disability Index to assess with a score range of 0 to 50.

  4. Global Perceived Effect Scale [two weeks]

    Change in the perception of the symptoms after the treatment was measured by a Global Perceived Effect Scale. Patients were asked to rate change between 1 completely recovered, 4 unchanged, 7 vastly worse on a horizontal likert scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis Nonspecific neck pain (NSNP)

  • Symptoms should last longer than 2 weeks

Exclusion Criteria:
  • Any known cause such as radiculopathy or neurological diseases,

  • History of neck surgery,

  • History of vertebral fracture,

  • Osteoporosis,

  • Tumor or a mass in the vertebral column,

  • Any spinal thrust manipulation contraindication,

  • Medication usage such as antiinflammatory or analgesic which might effect outcome assessments,

  • History of spinal manipulation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Abant Izzet Baysal University Bolu Merkez Turkey 14100
2 Health Sciences Faculty Bolu Abant Izzet Baysal University Bolu Merkez Turkey 14100

Sponsors and Collaborators

  • Abant Izzet Baysal University

Investigators

  • Principal Investigator: Erdal Dilekçi, MD, Bolu Abant Izzet Baylsa University
  • Principal Investigator: Ramazan KURUL, Ph.D, Bolu Abant Izzet Baylsa University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ramazan KURUL, Assistant Professor, Abant Izzet Baysal University
ClinicalTrials.gov Identifier:
NCT04455048
Other Study ID Numbers:
  • AIBU-FTR-RK-04
First Posted:
Jul 2, 2020
Last Update Posted:
Jul 13, 2021
Last Verified:
Jul 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ramazan KURUL, Assistant Professor, Abant Izzet Baysal University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 13, 2021