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RCT of Addition of 3D Posture Corrective Orthosis to A Multimodal Program of Treatment Of Chronic Postural Neck Pain.

Primary Purpose

Neck Pain

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Study or Experimental Group
Sponsored by
Huang Xiaolin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neck Pain

Eligibility Criteria

17 Years - 40 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male and female subjects with age from 17-40 years old.
  • Neck pain with equal or greater than 3/10 on a The Numeric Pain Rating Scale (NPRS) and the pain lasted more than 3 months (chronic neck pain).
  • Participants with neck disability at least score on neck disability index (NDI) was 5 from the total score 50.
  • Participants were included if they had posture deviations by screening test using GPS
  • Posture displacements:

    1. An anterior head translation more than 2.5 cm.
    2. Side shifting of the head in related to thoracic more than .5 cm.

Posture rotations:

  1. Rotation of head more than or equal three degrees.
  2. Side bending of the head more than or equal three degrees.
  3. Flexion or extension position of the head, normal angle 18 degrees, if more than that degree, it is meaning extension in upper cervical and if less means flexion in upper cervical. Participants included if they had at least two posture deviations whatever displacements or rotations. We included more obvious degrees or displacement of head posture related to thoracic to avoid variability of measurement between people and the posture deviations could be appeared and examined by visual examination.

    • If subjects could be able to continue treatment for 10 weeks then for 3 months of follow up.
    • If Participants accepted and signed an informed consent form.

Exclusion Criteria:

• If Participant reported any of the following conditions: Neck pain associated with whiplash injuries, medical red flag history(such as a tumor, fracture, metabolic diseases, rheumatoid arthritis, and osteoporosis).

  • Neck pain with cervical radiculopathy, neck pain associated with externalized cervical disc herniation.
  • Fibromyalgia syndrome, to avoid the similarity of fibromyalgia with an NP diagnosis, a physician used the criteria for the clinical diagnosis of fibromyalgia according to the American College of Rheumatology.
  • If the patient made surgery in the neck area before whatever the cause of operation.
  • Neck pain accompanied by vertigo caused by vertebrobasilar insufficiency or accompanied by non-cervicogenic headaches.
  • People were excluded if they were undergoing any type of pain treatment they have psychiatric disorders or other problems that contraindicate the use of the techniques in this study.
  • If Participants reported any of the following conditions: (1) a history of cervical or facial trauma or surgery. (2) Congenital anomalies involving the spine (cervical, thoracic, lumbar). (3) Bony abnormalities such as scoliosis.(4) Any systemic arthritis. (5) Recurrent middle ear infections over the last5 years or any hearing impairment requiring the use of a hearing aid. (6)Persistent respiratory difficulties over the last 5 years that had necessitated absence from work, required long-term medication or interfered with daily activities. (7) Any visual impairment not corrected by glasses. (8) Any disorder of the central nervous system. (9) pregnancy or breastfeeding because these conditions affect head posture.
  • Participants could be unable to attend a 10-week treatment program and follow-up as¬sessments after 3 months.

Sites / Locations

  • TongjiHospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional treatment

Study or Experimental Group

Arm Description

Usual Care Group: Conventional treatment: moist hot pack. manual therapy, Therapeutic Exercise.Home program routine.

moist hot pack. manual therapy. Therapeutic Exercise. Home program routine. 5.3D PCO to make mirror image therapy (reverse posture training) during the patient walking on motorized treadmill. For 10 weeks(3Times/week for 20 minutes).

Outcomes

Primary Outcome Measures

Neck Disability Index, assessing change of disability of neck patients
The NDI is a modification of the Oswestry Low Back Pain Disability Index. It is a patient-completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation. The NDI has sufficient support and usefulness to retain its current status as the most commonly used self-report measure for neck pain The NDI can be scored as a raw score [2]or doubled and expressed as a percent [3]. Each section is scored on a 0 to 5 rating scale, in which zero means 'No pain' and 5 means worst imaginable pain'. All the points can be summed to a total score. The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage.0 points or 0% means no activity limitations, 50 points or 100% means complete activity limitation.
Three-dimensional posture parameters of the head in relation to thoracic measured by global posture system (GPS) device.assessing the change of posture of neck patients
Postural translation of the head Tx(mediolateral translation ) Tz(anteroposterior translation ) Postural rotations of the head 1.Rx(flexion or extension position) 2.Ry (r.t rot. or l.t rot.) 3.Rz (r.t side bending or l.t side bending)

Secondary Outcome Measures

The Numeric Pain Rating Scale (NPRS)
is an 11-point numeric pain intensity ranging from 0 ('no pain') to 10 ('as much pain as possible'). A change of two points or more was identified as the minimal clinically important difference in patients with chronic neck pain.
Active cervical ROM using CROM
with an inclinometer (CROM Deluxe model, Performance Attainment Associates, Lindstrom, Minnesota).The CROM consists of 2 gravity-dependent goniometers, one compass dial, and a head-mounted frame allowing measurement of ROM in 3 planes (flexion/ extension, lateral flexion, rotation). A magnetic yoke consisting of 2 bar magnets held anteriorly and posteriorly was provided to reduce the influence of thoracic rotation. The CROM has demonstrated good concurrent validity for active ROM. According to the systematic review by Chen et al, the mean normative values of cervical ROM were determined to be: 52 degrees for flexion, 71 degrees for the extension, 72degrees for rotation, and 43 degrees for lateral flexion. Documentation of cervical ROM was rendered in the form of the full range (ie, a total value for the sagittal, frontal, or transverse plane, yielding 3 measurements).
Zung Self-Rating Anxiety Scale (SAS)
The SAS test is self-administered, with each response using a 4-point scale, from 'none of the time" to "most of the time." There are 20 questions with 15 increasing anxiety level questions and 5 decreasing anxiety questions. There are two formats, self-evaluations, and clinical evaluations.
Tampa Scale of Kinesiophobia (TSK)
Kinesiophobia was assessed with the 13-item Chinese version of the Tampa Scale of Kinesiophobia (TSK)

Full Information

First Posted
January 8, 2020
Last Updated
September 16, 2020
Sponsor
Huang Xiaolin
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1. Study Identification

Unique Protocol Identification Number
NCT04263883
Brief Title
RCT of Addition of 3D Posture Corrective Orthosis to A Multimodal Program of Treatment Of Chronic Postural Neck Pain.
Official Title
Randomized Control Trial of Addition of 3D Posture Corrective Orthosis to A Multimodal Program of Treatment Of NSNP.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
November 2020 (Anticipated)
Study Completion Date
November 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Huang Xiaolin

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
Nonspecific neck pain (NSNP) is one of the most common musculoskeletal problems treated by orthopedic physicians and physiotherapists. NSNP has an annual incidence rate of 38 to 73% and a lifetime prevalence of approximately 48%, leading to both economic and social problems.Due to increased disability-adjusted life-years from 17 million (95% confidence interval (CI): 11.4-23.7) in 1990 to 29 million (95% CI: 19.5-40.5) in 2016, Chronic neck pain is a common musculoskeletal disorder worldwide. No specific cause for neck symptoms assigned for most patients so it described as non-specific chronic neck pain (NSNP)
Detailed Description
Although the exact relationship between posture and NSNP is unsettled, the posture of the cervical spine appears to influence dorsal neck muscle activity at rest and during movement. Additionally, the forward head posture associated with thoracic kyphosis indirectly affects cervical flexion and rotational range of motion (ROM) also sustained computer work and prolonged using smart phones often in positions that encourage a functional kyphosis, appears to modify neck posture, as well as scapular positioning and upper trapezius muscle activity. Besides that Ergonomic intervention, including adjustments of the workplace station and postural correction, have been demonstrated to be effective in reducing NP with some work conditions. In addition, modalities that used to correct sagittal alignment of the cervical spine proved statistical and clinically significant results related to pain, disability, and improved nerve function. That is accomplish cause and effect relationship between bad posture and neck symptoms. According to the systematic review of Anabela et al., about head posture assessment useful for neck patients or not? The answer, of course, was yes, but it must be considered in relation to the patient's symptoms and related functional problems. Harrison and his colleagues reported that posture abnormalities occurred in the head, ribs, and pelvis in three dimensions in the form of translations and rotational displacements. Therefore, we should consider three dimensional (3D)postural assessment and correction during the treatment of NSNP associated with significant posture problems of the head in relation to thoracic. Growing research about using mirror image traction during ambulatory exercise, which is prescribed specifically to help normalize the patient's neuromuscular dysfunction and postural deformation via reflecting the patient's posture across different planes, is more beneficial than a less personalized program. With these considerations in mind and to combine the findings of 3D postural assessment into the treatment program, we designed adjustable 3D posture corrective orthotic (PCO) to be worn by the patient for a short time. The device has the ability to reflect all transitional displacements and rotational movements of the head then ask the patient to make ambulatory exercise using a treadmill while the PCO holds the patient's reverse posture. To our knowledge, no randomized clinical trial (RCT) had evaluated the addition of a 3D adjustable PCO to usual care program and investigate its short- and moderate-term improvement effects on NSNP management outcomes (i.e., neck pain, neck disability and 3-dimensional posture parameters of the head). The primary aim of our study was to evaluate of conducting an RCT using neck disability index (NDI )and 3D posture parameters. The secondary aim was NPRS and Active CervicalROM. investigate the effect size of the addition of ambulatory mirror-image traction via the wearing of 3D adjustable PCO compared to control group interventions for neck pain, disability, and 3D posture parameters.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional treatment
Arm Type
Active Comparator
Arm Description
Usual Care Group: Conventional treatment: moist hot pack. manual therapy, Therapeutic Exercise.Home program routine.
Arm Title
Study or Experimental Group
Arm Type
Experimental
Arm Description
moist hot pack. manual therapy. Therapeutic Exercise. Home program routine. 5.3D PCO to make mirror image therapy (reverse posture training) during the patient walking on motorized treadmill. For 10 weeks(3Times/week for 20 minutes).
Intervention Type
Device
Intervention Name(s)
Study or Experimental Group
Intervention Description
3D PCO to make mirror image therapy (reverse posture training) during the patient walking on motorized treadmill, This way of functional training will deliver via the use of the adjustable cervicothoracic orthosis during the patient walking at approximately 2-3 miles per hour on a standard, motorized treadmill. The brace will reverse the abnormal posture according to the 3D posture analysis data. To facilitate tissue remodeling by reverse posture training, this called mirror image traction.then the ambulatory exercises by using treadmill will be performed while the patient's mirror image posture will be held by the adjustable orthosis, ambulatory exercises for 20 minutes by using treadmill based on Harrison et al., approach, this program will be repeated 2-3 times /week for 10weeks.
Primary Outcome Measure Information:
Title
Neck Disability Index, assessing change of disability of neck patients
Description
The NDI is a modification of the Oswestry Low Back Pain Disability Index. It is a patient-completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation. The NDI has sufficient support and usefulness to retain its current status as the most commonly used self-report measure for neck pain The NDI can be scored as a raw score [2]or doubled and expressed as a percent [3]. Each section is scored on a 0 to 5 rating scale, in which zero means 'No pain' and 5 means worst imaginable pain'. All the points can be summed to a total score. The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage.0 points or 0% means no activity limitations, 50 points or 100% means complete activity limitation.
Time Frame
Pre treatment at 1st day , post treatment after 10 weeks , follow up after 6 months.
Title
Three-dimensional posture parameters of the head in relation to thoracic measured by global posture system (GPS) device.assessing the change of posture of neck patients
Description
Postural translation of the head Tx(mediolateral translation ) Tz(anteroposterior translation ) Postural rotations of the head 1.Rx(flexion or extension position) 2.Ry (r.t rot. or l.t rot.) 3.Rz (r.t side bending or l.t side bending)
Time Frame
Pre treatment at 1st day , post treatment after 10 weeks , follow up after 6 months.
Secondary Outcome Measure Information:
Title
The Numeric Pain Rating Scale (NPRS)
Description
is an 11-point numeric pain intensity ranging from 0 ('no pain') to 10 ('as much pain as possible'). A change of two points or more was identified as the minimal clinically important difference in patients with chronic neck pain.
Time Frame
Pre treatment at 1st day , post treatment after 10 weeks , follow up after 6 months.
Title
Active cervical ROM using CROM
Description
with an inclinometer (CROM Deluxe model, Performance Attainment Associates, Lindstrom, Minnesota).The CROM consists of 2 gravity-dependent goniometers, one compass dial, and a head-mounted frame allowing measurement of ROM in 3 planes (flexion/ extension, lateral flexion, rotation). A magnetic yoke consisting of 2 bar magnets held anteriorly and posteriorly was provided to reduce the influence of thoracic rotation. The CROM has demonstrated good concurrent validity for active ROM. According to the systematic review by Chen et al, the mean normative values of cervical ROM were determined to be: 52 degrees for flexion, 71 degrees for the extension, 72degrees for rotation, and 43 degrees for lateral flexion. Documentation of cervical ROM was rendered in the form of the full range (ie, a total value for the sagittal, frontal, or transverse plane, yielding 3 measurements).
Time Frame
Pre treatment at 1st day , post treatment after 10 weeks , follow up after 6 months.
Title
Zung Self-Rating Anxiety Scale (SAS)
Description
The SAS test is self-administered, with each response using a 4-point scale, from 'none of the time" to "most of the time." There are 20 questions with 15 increasing anxiety level questions and 5 decreasing anxiety questions. There are two formats, self-evaluations, and clinical evaluations.
Time Frame
Pre treatment at 1st day , post treatment after 10 weeks , follow up after 6 months.
Title
Tampa Scale of Kinesiophobia (TSK)
Description
Kinesiophobia was assessed with the 13-item Chinese version of the Tampa Scale of Kinesiophobia (TSK)
Time Frame
Pre treatment at 1st day , post treatment after 10 weeks , follow up after 6 months.
Other Pre-specified Outcome Measures:
Title
Global Perceived Effect Questionnaire (GPE)
Description
The perceived effect of the intervention was assessed with the Global Perceived Effect Questionnaire. 5-point Likert-type scale used to evaluate self-reported improvement or deterioration after the intervention. The use of the GPE is widely reported in the physical therapy literature. Patient satisfaction was assessed with the Chinese version of the PhysicalTherapy Patient Satisfaction Questionnaire (PTPSQ-I[ which demonstrated good psychometric properties and a 2-factor structure, related to perceived "overall experience" and "professional impression." (GPE),
Time Frame
post treatment after 10 weeks , follow up after 6 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
17 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female subjects with age from 17-40 years old. Neck pain with equal or greater than 3/10 on a The Numeric Pain Rating Scale (NPRS) and the pain lasted more than 3 months (chronic neck pain). Participants with neck disability at least score on neck disability index (NDI) was 5 from the total score 50. Participants were included if they had posture deviations by screening test using GPS Posture displacements: An anterior head translation more than 2.5 cm. Side shifting of the head in related to thoracic more than .5 cm. Posture rotations: Rotation of head more than or equal three degrees. Side bending of the head more than or equal three degrees. Flexion or extension position of the head, normal angle 18 degrees, if more than that degree, it is meaning extension in upper cervical and if less means flexion in upper cervical. Participants included if they had at least two posture deviations whatever displacements or rotations. We included more obvious degrees or displacement of head posture related to thoracic to avoid variability of measurement between people and the posture deviations could be appeared and examined by visual examination. If subjects could be able to continue treatment for 10 weeks then for 3 months of follow up. If Participants accepted and signed an informed consent form. Exclusion Criteria: • If Participant reported any of the following conditions: Neck pain associated with whiplash injuries, medical red flag history(such as a tumor, fracture, metabolic diseases, rheumatoid arthritis, and osteoporosis). Neck pain with cervical radiculopathy, neck pain associated with externalized cervical disc herniation. Fibromyalgia syndrome, to avoid the similarity of fibromyalgia with an NP diagnosis, a physician used the criteria for the clinical diagnosis of fibromyalgia according to the American College of Rheumatology. If the patient made surgery in the neck area before whatever the cause of operation. Neck pain accompanied by vertigo caused by vertebrobasilar insufficiency or accompanied by non-cervicogenic headaches. People were excluded if they were undergoing any type of pain treatment they have psychiatric disorders or other problems that contraindicate the use of the techniques in this study. If Participants reported any of the following conditions: (1) a history of cervical or facial trauma or surgery. (2) Congenital anomalies involving the spine (cervical, thoracic, lumbar). (3) Bony abnormalities such as scoliosis.(4) Any systemic arthritis. (5) Recurrent middle ear infections over the last5 years or any hearing impairment requiring the use of a hearing aid. (6)Persistent respiratory difficulties over the last 5 years that had necessitated absence from work, required long-term medication or interfered with daily activities. (7) Any visual impairment not corrected by glasses. (8) Any disorder of the central nervous system. (9) pregnancy or breastfeeding because these conditions affect head posture. Participants could be unable to attend a 10-week treatment program and follow-up as¬sessments after 3 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmed Youssef, PHD Student
Phone
0086 -13129937059
Email
dr.ahmedsameer@pt.bsu.edu.eg
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaolin Huang, professor
Phone
8613871261957
Email
xiaolinh2006@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaolin Huang, Professor
Organizational Affiliation
Tongji Hospital
Official's Role
Study Director
Facility Information:
Facility Name
TongjiHospital
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
432000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaolin Huang, Professor
Phone
8613871261957
Email
xiaolinh2006@126.com
First Name & Middle Initial & Last Name & Degree
Ahmed Youssef, PHD Student
Phone
0086 -13129937059
Email
dr.ahmedsameer@pt.bsu.edu.eg

12. IPD Sharing Statement

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RCT of Addition of 3D Posture Corrective Orthosis to A Multimodal Program of Treatment Of Chronic Postural Neck Pain.

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