FHP: Effect of Cervical Stability Training on Somatosensory Evoked Potential and Cervical Spine in Forward Head Posture

Sponsor
Cairo University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05149183
Collaborator
(none)
40
1
2
2.5
16

Study Details

Study Description

Brief Summary

to investigate the effect of cervical stability training on somatosensory evoked potential and cervical spine in forward head posture

Condition or Disease Intervention/Treatment Phase
  • Other: cervical stability training
  • Other: traditional treatment
N/A

Detailed Description

The use of electronic tools is increasing in worldwide varieties and the attractiveness of these tools lead to variety of groups of people, especially teenagers, using them for prolonged period of time leading to increased musculoskeletal problems. Excessive use of smartphones for long period of time can lead to decreased postural control and forward head postur (FHP) as phone users maintain an abnormal alignment of the head and neck. The habit of repetitive use of computers, TV, mobile phones, and video games and even back packs forces the body to exhibit bad posture. The overall prevalence of FHP was reported to be 66% in computer based workers.

cervical stability training play a major role in treatment of forward head posture so this study will be conducted to investigate its role on craniovertebral angle, cervical range of motion, pain intensity level, functional disability, neck flexor and extensor muscles endurance, lordotic cervical curvature, somatosensory evoked potential in forward head patient.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
this trial has two groups, one experimental and one controlthis trial has two groups, one experimental and one control
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
opaque sealed envelope
Primary Purpose:
Treatment
Official Title:
Effect of Cervical Stability Training on Somatosensory Evoked Potential and Cervical Spine in Forward Head Posture
Anticipated Study Start Date :
Dec 15, 2021
Anticipated Primary Completion Date :
Mar 1, 2022
Anticipated Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: cervical stability training

cervical stability training will be received three times a week for eight weeks

Other: cervical stability training
cervical stability training will be contain three phases, each phase has six positions ( supine, forearms, sidelying, four point kneeling, sitting and standing position)

Other: traditional treatment
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.

Active Comparator: traditional treatment

traditional treatment will be received three times a week for eight weeks

Other: traditional treatment
TENS, hot packs, stretching exercise of superficial neck muscles, and postural advice.

Outcome Measures

Primary Outcome Measures

  1. somatosensory evoked potential [up to eight weeks]

    somatosensory evoked potential will be measured by electromyograph device

  2. craniovertebral angle [up to eight weeks]

    craniovertebral angle will be measured photographically by surgimap program

Secondary Outcome Measures

  1. pain intensity level [up to eight weeks]

    pain will be measured by visual analogue scale

  2. functional disability [up to eight weeks]

    disability will be measured by arabic neck disability index

  3. cervical range of motion [up to eight weeks]

    Phone application (clinometer) will used to measure cervical range of motion using smartphone (Infinix Note 5)

  4. endurance test [up to eight weeks]

    flexion and extension endurance will be measured using pressure biofeedback unit

  5. cervical curvature [up to eight weeks]

    digital x ray will be used to measure cervical curvature

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Adult participant (18-to-40years old) with forward head posture, BMI 20-to-25 kg/m², The area of mechanical neck pain will defined to the cervical region, possibly with referred pain into the occipit, nuchal muscles, and shoulders, All patients will have chronic neck pain for more than 3 months, Craniovertebral angle of ˂ 49.

Exclusion Criteria:

Signs of serious pathology (e.g., rheumatoid diseases, ankylosing spondylitis), History of cervical spine surgery, History of trauma or fractures in cervical spine, Signs of cervical radiculopathy or myelopathy, Vascular syndrome such as vertebrobasilar insufficiency.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Salah Eid Ahmed Ali Giza Egypt 11251

Sponsors and Collaborators

  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Al Shaymaa Shaaban Abd El Azeim, lecturer, Cairo University
ClinicalTrials.gov Identifier:
NCT05149183
Other Study ID Numbers:
  • P.T.REC/012/003459
First Posted:
Dec 8, 2021
Last Update Posted:
Dec 8, 2021
Last Verified:
Nov 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Al Shaymaa Shaaban Abd El Azeim, lecturer, Cairo University

Study Results

No Results Posted as of Dec 8, 2021