NCT06732557

Brief Summary

sixty patients with forward head posture will be randomized to three groups Group A: will receive traditional treatment ( isometric exercise for deep neck flexors plus sub occipital release). Group B: will receive traditional treatment plus muscle energy technique for upper trapezius, elevator scapulae and sternocleidomastoid. Group C: will receive traditional treatment plus mulligan mobilization

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2024

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

December 7, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 13, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2025

Completed
Last Updated

December 13, 2024

Status Verified

December 1, 2024

Enrollment Period

2 months

First QC Date

December 7, 2024

Last Update Submit

December 12, 2024

Conditions

Keywords

forward head postureMulligan MobilizationMuscle energy technique

Outcome Measures

Primary Outcomes (4)

  • Pain

    Pain will be measured by visual analogue scale which is a valid and reliable scale for measuring pain starts with zero (represents no pain) and ends with 10 (represents maximum pain).

    Before the first session and at the end of the treatment program ( one month)

  • Cervical range of motion

    Cervical range of motion in will be measured by cervical range of motion basic assessment device (CROM) the angle of cervical range of motion will be recorded in degrees to determine the limitation in range of motion

    Before the first session and after the end of the treatment program ( one month)

  • Disability measurement

    Disability will be measured by neck disability index(NDI) is a valid and reliable scale. The NDI consists of ten questions in the following domains: Pain Intensity, Personal Care, Lifting, Reading, Headaches, Concentration, Work, Driving, Sleeping, and Recreation. Scoring: Each question contains six answer choices, scored from 0 (no disability) to 5 (complete disability). All section scores are then totaled. Scoring is reported on a 0-50 scale, 0 being the best possible score and 50 being the worst. Alternately, the score can be reported from 0-100. The score is often reported as a percentage (0-100%).

    Before the first session and after the end of the treatment program ( one month)

  • Cervicovertebral angle

    Cervicovertebral angle (CVA) Will be measure by kinovea: Normal range is between 55 and 86, If the angle is less than 50 degrees, it will be considered to be FHP. Adhesive markers (8 mm in diameter) will be placed on the participant's C7 spinous process and tragus of the ear. The physical therapist will observe the participant from the lateral side while standing and then take a picture of the participant from a fixed distance (75 cm) and height (150 cm), then with the help of an application sealed by a password which is called KINOVEA, the angle will be measured by placing each vector as following a line from the tragus of the ear to the C7 spinous process and another horizontal line through the C7 spinous. The angle will be recorded in degrees

    Before the first session and after the end of the treatment program ( one month)

Study Arms (3)

Group A: Control group (Traditional treament)

SHAM COMPARATOR

patients will receive traditional treatment (isometric exercise for deep neck flexors plus sub occipital release).

Other: Traditional treatments

Group B (muscle energy technique group)

EXPERIMENTAL

Patients will receive muscle energy Technique for upper trapezius, elevator scapulae and sternocleidomastoid

Other: Traditional treatmentsOther: muscle energy technique

Group C (Mulligan Mobilization Group)

ACTIVE COMPARATOR

Patients will receive Mulligan mobilization

Other: Traditional treatmentsOther: Mulligan Mobilization

Interventions

Isometric exercise for deep neck flexors and sub occipital release

Group A: Control group (Traditional treament)Group B (muscle energy technique group)Group C (Mulligan Mobilization Group)

Muscle energy technique for upper trapezius, elevator scapulae and sternocleidomastoid

Group B (muscle energy technique group)

Mulligan mobilization in the form of SNAGS for rotation, lateral flexion, extension and flexion

Group C (Mulligan Mobilization Group)

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 18 to 45 years
  • Non specific neck pain reproduced by neck movement
  • Neck pain at least within the last three months
  • Limitation in cervical range of motion

You may not qualify if:

  • cervical spine surgery or injury
  • neurologic deficits, infection or inflammation
  • cervicogenic headache

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

Central Study Contacts

Radwa fayek Lecturer at Basic Science Department MTI University, Doctoral

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
teaching assistant of Basic Science Department

Study Record Dates

First Submitted

December 7, 2024

First Posted

December 13, 2024

Study Start

December 1, 2024

Primary Completion

February 1, 2025

Study Completion

February 1, 2025

Last Updated

December 13, 2024

Record last verified: 2024-12