NCT05274711

Brief Summary

To investigate if the Whole-body vibration affect cervical function cervical, proprioception, pain intensity level and ROM and in subjects with forward head posture?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 2, 2022

Completed
8 days until next milestone

First Posted

Study publicly available on registry

March 10, 2022

Completed
4 months until next milestone

Study Start

First participant enrolled

July 1, 2022

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2023

Completed
27 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2023

Completed
Last Updated

May 26, 2023

Status Verified

May 1, 2023

Enrollment Period

7 months

First QC Date

March 2, 2022

Last Update Submit

May 25, 2023

Conditions

Outcome Measures

Primary Outcomes (2)

  • The change in Neck disability

    Neck disability will be measured by English neck disability index (NDI) questionnaire is composed of a total of 10 questions. Each question has 6 answer options which pertain to a level of severity (0-5) With total score of 50 , when NDI is high the neck function is the worst

    immediately after the treatment

  • The change in Neck proprioception

    Neck proprioception will be measured by clinometer application

    immediately after the treatment

Secondary Outcomes (2)

  • Neck pain

    Before and immediately after the treatment

  • Cervical ROM

    Before and immediately after the treatment

Study Arms (2)

Conventional treatment

ACTIVE COMPARATOR

will receive conventional physical therapy prograM

Other: Conventional physical treatment

Experimental treatment

EXPERIMENTAL

will receive conventional physical therapy program and whole body vibration training

Other: Whole body vibration trainingOther: Conventional physical treatment

Interventions

The participants will be instructed to stand on the vibration platform bare footed and distribute their weight evenly on both feet (fig 3). Next, they will be asked to do a head and neck retraction while looking forward with their knees at 30 degrees of flexion. In order to prevent fatigue in the subject's cervical area due to holding their head and neck in retraction, they will be asked to hold this position for 15 seconds then rest for 5 seconds. Since each set will last 60 second this allowed the subjects to do 3 retractions in each set. In total each subject will perform 15 retractions during the training. The subjects will experience a vertical vibration at a frequency and amplitude of 30 Hz and 4 mm during the sets (Salami et al., 2018).

Experimental treatment

Posturalcorrectionexercisesintheformofstretchingandstrengthening exercise. Manual stretching exercises as passive stretch to (upper trapezius, levator scapulae, sub occipitalis, scalene, sternocleidomastoid, and pectoralis major muscles), 30 seconds of 3-5 repetitions for each muscle, followed by 30 seconds of rest, as well as isotonic exercises (to strength deep neck flexors and scapular retractor muscles) 3 sets of 12 repetitions each with a 6 second hold in between, with a 1-2-minute rest between sets (Kisner. and Colby 2012).

Conventional treatmentExperimental treatment

Eligibility Criteria

Age18 Years - 23 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Adolescent physical therapy students of both gender between 18-23 years old
  • BMI between 18.5-25 kg/m²
  • Symptomatic forward head posture with CVA 49° or less.

You may not qualify if:

  • Cervical disc
  • Myelopathy or cervical radiculopathy
  • Cervical spine surgery in the past
  • Having received physical therapy in the three months prior to the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aya Ali saaid mahmoed

Cairo, 11311, Egypt

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
Opaque sealed envelope
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This trail has 2 groups one control and one experimental
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant lecturer

Study Record Dates

First Submitted

March 2, 2022

First Posted

March 10, 2022

Study Start

July 1, 2022

Primary Completion

February 1, 2023

Study Completion

February 28, 2023

Last Updated

May 26, 2023

Record last verified: 2023-05

Locations