NCT07790874

Brief Summary

To investigate the effects of oculomotor exercises on pain disability, dizziness and gaze stability in patients with non-traumatic cervical dizziness.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Aug 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress32%
Aug 2026Oct 2026

Study Start

First participant enrolled

August 11, 2026

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

August 25, 2026

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 27, 2026

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 16, 2026

Expected
24 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 10, 2026

Last Updated

August 27, 2026

Status Verified

August 1, 2026

Enrollment Period

1 month

First QC Date

August 25, 2026

Last Update Submit

August 25, 2026

Conditions

Keywords

cervical dizzinessOculomotor ExercisesGaze StabilityNon Traumatic

Outcome Measures

Primary Outcomes (4)

  • Rating Scale of Gaze Stability

    Assesses gaze stability during head movements in sitting. It consists of three ratings: 0 indicates stable gaze, 1 indicates slightly irregular gaze stability, and 2 indicates repeatedly unstable gaze.

    4 weeks

  • Neck Disability index

    It comprises of 10 items; 7 related to daily living activities, 2 related to pain and 1 related to concentration. Each item is scored from 0 to 5. Total score is expressed as a percentage, with higher scores related to greater disability. It has high test-retest reliability (ICC = 0.978)

    4 weeks

  • Dizziness Handicap Inventory questionnaire

    A 25-item questionnaire assessing the functional, emotional, and physical effects of dizziness. Each item is scored as 0, 2, or 4, with a total score ranging from 0-100. Lower scores indicate less disability.

    4th week

  • Universal Goniometer

    A commonly used instrument for measuring cervical range of motion. It demonstrates high test-retest reliability and inter-rater reliability.

    4 weeks

Study Arms (2)

Sustained Natural Apophyseal Glides and Oculomotor Exercises

EXPERIMENTAL

Participants in Group A received moist heating pad, isometric exercises, Sustained Natural Apophyseal Glides, and oculomotor exercises including saccadic eye movements, smooth pursuit training, gaze stabilization, and head-eye coordination exercises.

Other: Sustained Natural Apophyseal Glides and Oculomotor exercises

Sustained Natural Apophyseal Glides

ACTIVE COMPARATOR

Participants in Group B received standard physiotherapy, consisting of moist heating pad, isometric exercises, and Sustained Natural Apophyseal Glides

Other: Sustained Natural Apophyseal Glides

Interventions

Sustained Natural Apophyseal Glides: The patient sat upright and actively moved the head in the direction that provoked dizziness. The therapist applied a sustained anterior glide to the targeted C1 or C2 vertebra during the movement. The technique was performed initially for 3 repetitions and progressed to 6 repetitions, with gentle overpressure added as tolerated. Oculomotor Exercises: The intervention included saccadic eye movements, smooth pursuit training, gaze stabilization, and head-eye coordination exercises. These exercises were performed with the head and/or eyes moving in controlled directions to improve gaze stability, eye-head coordination, and sensorimotor control.

Also known as: SNAGs
Sustained Natural Apophyseal Glides and Oculomotor Exercises

he patient sat upright and actively moved the head in the direction that provoked dizziness. The therapist applied a sustained anterior glide to the targeted C1 or C2 vertebra during the movement. The technique was performed initially for 3 repetitions and progressed to 6 repetitions, with gentle overpressure added as tolerated.

Sustained Natural Apophyseal Glides

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Both Males and Females
  • Age between 20 and 40 years with nontraumatic cervical dizziness.
  • Patients experiencing symptoms of cervicogenic dizziness for at least 3 months (chronic cervicogenic dizziness)
  • Patients having a Numeric Pain Rating Scale (NPRS) score greater than or equal to 3
  • Patient with positive Flexion Rotation Test (FRT)
  • Cervical Torsion Test
  • Patients have never received oculomotor exercises and SNAGS before.

You may not qualify if:

  • History of trauma or recent surgery to the head, face, neck, or chest.
  • Diagnosis of central vertigo (e.g., brainstem or cerebellar pathology).
  • Presence of vestibular-origin vertigo, such as benign paroxysmal positional vertigo (BPPV).
  • Triage (Patients with traumatic cervical spine injury, Cervical arterial dysfunction and central vestibular disorders
  • Inability to perform exercises (e.g., due to cervical fracture)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Independent Hospital

Faisalābad, Punjab Province, 38000, Pakistan

RECRUITING

MeSH Terms

Conditions

DizzinessPain

Condition Hierarchy (Ancestors)

Sensation DisordersNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Saba Rafiq, PhD

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The assessor was blind to the treatment groups to guarantee accuracy and minimize bias.
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 25, 2026

First Posted

August 27, 2026

Study Start

August 11, 2026

Primary Completion (Estimated)

September 16, 2026

Study Completion (Estimated)

October 10, 2026

Last Updated

August 27, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations