Cervical Spine Strengthening Exercises Versus Kendall Exercises in Patients With Forward Head Posture.

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05878600
Collaborator
(none)
38
1
2
9
4.2

Study Details

Study Description

Brief Summary

To compare the effects of targeted cervical spine strengthening exercises and Kendall exercise in patients with forward head posture

Condition or Disease Intervention/Treatment Phase
  • Other: kendall's exercise
  • Other: cervical spine strengthening
N/A

Detailed Description

Studies have evaluated the effect of Kendall's exercises and found it effective for recovery. Studies have also concluded that targeted strengthening of flexors reverse the symptoms. The purpose of this study will elaborate either there is a difference in time taken to achieve normal head alignment between a targeted muscle that is prone to weakness or a technique that involves strengthening of weakened muscle plus stretching of shortened muscles. As there is a vast variety of correcting exercise program in the literature, the decision to choose the best option may be challenging. This study may help physiotherapists to apply treatment that is directly directing the main culprit.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Targeted Cervical Spine Strengthening Exercises Versus Kendall Exercises in Patients With Forward Head Posture.
Actual Study Start Date :
Nov 16, 2022
Anticipated Primary Completion Date :
Jul 16, 2023
Anticipated Study Completion Date :
Aug 16, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: cervical spine strengthening group

The participant will nod and chin tuck the head against the block with bands supporting the movement. An air-filled pressure cushion is placed under the occiput behind the cervical spine and conforms to the subject's shape. With a head nod, the pressure on the cuff increases and is shown by the dial. 10 repetitions of 5 seconds hold will be performed for 8 weeks and strength is measured by sphygmomanometer

Other: cervical spine strengthening
sole effect of cervical spine strengthening will be analyzed

Active Comparator: Kendall exercise group

patient is seated and the exercises are performed which include stretching pectoralis muscle, placing both hands on the occipital area and pulling the elbows back up and performing arm abduction and external rotation; and (2) strengthening shoulder retraction, Strengthening the deep cervical flexors and Stretching the cervical extensors

Other: kendall's exercise
comparative effect of targeted cervical spine strengthening versus kendalls exercise will be analyzed
Other Names:
  • cervical spine strengthening
  • Outcome Measures

    Primary Outcome Measures

    1. Change in NPRS [8th week]

      Pain intensity will be assessed by numeric pain rating scale NPRS. The 11-point NPRS (intervals from 0-10) is used to quantify pain intensity; 0 represents no pain, and 10 represent the worst possible agony. The NPRS is a valid and reliable instrument for older persons. Participants will be asked to select the number that most accurately describes their level of pain. At the baseline assessment, following each exercise session during the 8-week intervention, and finally at the end of the intervention Programmed, the NPRS scores will be recorded Changes from Basline to 8th week

    Secondary Outcome Measures

    1. Range of motion [8th week]

      A goniometer is a device that measures an angle or permits the rotation of an object to a definite position. The long arm goniometers are more accurate for joints with long levers like the knee and hip joints. A universal goniometer has three parts. A body: It is designed like a protractor and may form a full or a half-circle. It has a scale for the measurement of the angle. The scale can extend either from 0 to 180 degrees or 180 to 0 degrees. A fulcrum: The screw-like device can be tightened to fix the moving arm in a particular position or loosened to permit free movement. The moving arm is the arm of the goniometer, which aligns with the mobile part of the joint measured. Changes from Basline to 8th week

    Other Outcome Measures

    1. neck disability index [8th week]

      The neck disability index NDI has become a standard instrument for measuring self-rated disability due to neck pain. Each of the 10 items scores from 0 to 5. The maximum score is 50 Changes from Basline to 8th week

    2. Photogrammetry [8th week]

      It is used for postural evaluation. Most common way to find forward head posture is y measuring craniovertebral angle. Photos were taken from patients' right side and analysis is done by using ImageJ software Changes from Basline to 8th week

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Both genders

    • Age 20-40 years with no signs of degeneration.

    • Individuals having cranio-vertebral angle less than 50

    • Those who have not gone under rehabilitation for last 6 months

    • Those who are computer users for more than 3 hours a day or more.

    Exclusion Criteria:
    • Spinal trauma

    • Musculoskeletal abnormality in the cervical spine

    • Rheumatologic disorders

    • Any bony or soft tissue systemic disease

    • Congenital defects

    • Disc pathology

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Bank of Punjab, Lahore Lahore Punjab Pakistan 54000

    Sponsors and Collaborators

    • Riphah International University

    Investigators

    • Principal Investigator: Rabiya Noor, PHD, Riphah International University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Riphah International University
    ClinicalTrials.gov Identifier:
    NCT05878600
    Other Study ID Numbers:
    • REC/RCR & AHS/23/0120
    First Posted:
    May 26, 2023
    Last Update Posted:
    May 26, 2023
    Last Verified:
    May 1, 2023
    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 Riphah International University

    Study Results

    No Results Posted as of May 26, 2023