- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05298631
Comparing the Effects of Neck Stabilization Exercises Verses Dynamic Exercises Among Patients Having Nonspecific Neck Pain With Forward Head Posture
May 5, 2023 updated by: Asma Batool, Dow University of Health Sciences
Comparing the Effects of Neck Stabilization Exercises Verses Dynamic Exercises Among Patients Having Nonspecific Neck Pain With Forward Head Posture- A Randomized Clinical Trial
the objective of this randomized clinical trial is to compare the effectiveness of neck stabilization exercises versus neck dynamic exercises in patients having non specific neck pain with forward head posture for pain intensity, correction of forward head posture, increasing Range of movement and decrease functional disability.
the study is being conducted at physiotherapy department of institute of physical medicine and rehabilitation (Dow university of health sciences) total 60 patients with non specific neck pain with forward head posture recruited by non-probability sampling technique initially screening done by consultant physicians who is blinded to the treatment given to patients.
patient are included in study who fulfill inclusion criteria and sign the consent form.
patients then randomly allocated to both treatment groups using computer generated randomization sheet.
baseline assessment is taken at first session after providing 9 treatment of stabilizing exercises to group1 and dynamic exercises to group 2 session post assessment will be done on goniometry, NDI, VAS and plumb line at last session at third week.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sindh
-
Karachi, Sindh, Pakistan, 75600
- Sindh Institute of Physical Medicine and Rehabilitation
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Patients with nonspecific neck pain more than 3 weeks less than 6 months.
- Patients with forward head posture on plumb line assessment.
- Pain on VAS moderate 4-7
- NDI score with moderate; 50-64%.
- Age ranges from 18-40.
Exclusion Criteria:
- Previous history of any accident (whiplash), fracture, tumor etc.
- Patients not willing to participate.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment group 1: stabilization exercises
stabilization exercises
|
The activation of deep cervical muscle to reduce the activity of surface muscles is known as stabilization exercises
|
|
Active Comparator: Treatment group 2: dynamic exercises
dynamic exercises
|
The exercises in which muscle tension remains constant but muscle length changes is known as dynamic exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in pain intensity with Visual analog scale (VAS) in cm
Time Frame: Baseline and 3 weeks
|
VAS will be used for assessment of pain intensity on 10 cm straight line with marking from 0 to 10 (0 means no pain and 10 means worst pain possible) patients pain is recorded at baseline at the start of 1st session than change in pain intensity (decrease) will be assessed at the end of 9th session at week 3.
|
Baseline and 3 weeks
|
|
Change in disability with Neck disability index questionnaire (NDI) scores
Time Frame: Baseline and 3 weeks
|
NDI will be used for the assessment of disability due to neck pain.
NDI is a ten item questionnaire each question has 6 responses from 0 no disability to 5 complete disability (score of less than 4 indicates no disability, 5-14 mild disability, 15-24 moderate disability, 25-34 severe disability, and scores greater than 35 complete disability) used to assess disability associated with neck pain and whiplash injury.
patients disability is recorded at baseline at the start of 1st session than change in disability (decrease) will be assessed at the end of 9th session at week 3.
|
Baseline and 3 weeks
|
|
Change in neck range of motions with goniometer in degrees
Time Frame: Baseline and 3 weeks
|
Goniometry will be used for the assessment of change in available range of motion of around neck joint in degrees.
the therapist assess the range of motion using goniometer in flexion, extension, lateral flexion(right), lateral flexion(left), rotation(right), rotation(left).
patients ROM is recorded at baseline at the start of 1st session than change in ROM (increase) will be assessed at the end of 9th session at week 3.
|
Baseline and 3 weeks
|
|
Change in ear position with reference to shoulder Plumb line measurement in inches
Time Frame: Baseline and 3 weeks
|
Plumb line measurement will be used for the assessment of forward head posture using body landmarks such as ear lobe or mastoid process and shoulder alignment in inches.
patients forward head is recorded at baseline at the start of 1st session than change in forward head (postural correction) will be assessed at the end of 9th session at week 3.
|
Baseline and 3 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Rabail Rani Soomro, MSPT, Sindh Institute of Physical Medicine and Rehabilitation
- Study Director: Aftab Ahmed Mirza Baig, MSAPT, Sindh Institute of Physical Medicine and Rehabo
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 6, 2022
Primary Completion (Actual)
January 17, 2023
Study Completion (Actual)
January 21, 2023
Study Registration Dates
First Submitted
March 17, 2022
First Submitted That Met QC Criteria
March 17, 2022
First Posted (Actual)
March 28, 2022
Study Record Updates
Last Update Posted (Actual)
May 8, 2023
Last Update Submitted That Met QC Criteria
May 5, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ABatool
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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