- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07327827
Comparative Effects of Back School Based Intervention Versus Cranio-Cervical Muscle Training in Computer Users With Cervicogenic Headache
January 23, 2026 updated by: Dr. Hufsa Tariq, Lahore University of Biological and Applied Sciences
Effects of Back School Based Intervention Versus Cranio-Cervical Muscle Training on Pain, Posture and Disability in Computer Users With Cervicogenic Headache
The aim of the study is to compare Back School Based Intervention with Cranio- Cervical muscle training in participants with Cervicogenic headache. The study wants to investigate that which intervention helps to mange pain, improve posture and reduce disability. The study aims to answer the question:
- How effective is Back School Based intervention on pain, posture and disability in computer users with Cervicogenic headache compared to Cranio-cervical Muscle Training? Participants will
- Attend the treatment sessions of the group in which they are placed.
- Take treatment session two times a week for eight weeks.
- Participants will be asked about their pain and activities throughout the study.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
- Headache is one of the disorder that affects 50% of the population worldwide which have negative impact on the quality of life. Cervicogenic headache is the secondary type of headache in which the pain referred from the cervical spine. Headache aggravates by the neck movement and significant reduced range of motion is noticed among patients.
- The management of the cervicogenic headache is both pharmacological and non- pharmacological but pharmacological having more side effects.Non pharmacological management includes massage, dry needing, physical therapy exercises, manual therapy and patient education.
- Cranio-cervical muscle training include cranio-cervical flexion exercises, strengthening, stretching, posture exercises and cervical stabilization exercises. These exercises altogether helps in the strengthening of the neck and shoulder muscles which ultimately correct the cervical impairment which neutralize the posture and decrease the load on the structures of the spine.
- Back school based exercise program can have both practical and theoretical sessions. In practical part patient is guided to the different strengthening and flexibility exercises with increase resistance in each session. In theoretical part patient education is the main part. Patient is educated about the anatomical and posture related changes in the spine so he/ she can identify and correct them by incorporating in their daily life.
Study Type
Interventional
Enrollment (Estimated)
44
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 Contact
- Name: Laiba Azam
- Phone Number: 0324-4714749
- Email: laibaazam99@gmail.com
Study Contact Backup
- Name: Hufsa Tariq
- Phone Number: 0331-6732797
- Email: hufsatariq@ubas.edu.pk
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Sir Ganga Ram Hospital Lahore
-
-
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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Participants of both gender.
- Participants aged between 19 to 44 years.
- Participants having unilateral headache without side shift for>3 months aggravated by neck movement.
- Participants with pain intensity ≥3 on a visual analog scale (VAS).
- Participants working on the computer for an average 32 h per week.
- Participants having positive cervical flexion rotation test (CFRT).
- Participants having joint tenderness in at least one of the upper three cervical joints with palpation.
Exclusion Criteria:
- If participants having any history of fractures or previous surgery of the vertebral column, any degenerative and inflammatory arthritis, osteoporosis, dislocations, cervical radiculopathy/myelopathy and any history of whiplash injury.
- Participants showing any signs of the five 'D's' or three 'N's.
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Back School Based Intervention
|
|
|
Active Comparator: Cranio- Cervical Muscle Training
Cranio- cervical muscle Training
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue scale
Time Frame: It will be measured at baselines, 4 weeks and at 8 weeks.
|
Visual Analogue Scale is used for the measurement of pain.a
hand written mark on 10 cm line helps to differentiate pain in different patients.
If Patient reports minimum pain level more than 3 than considered as the patient required for study maximum pain level will be 10
|
It will be measured at baselines, 4 weeks and at 8 weeks.
|
|
Headache Disability Index
Time Frame: It will be measured at baseline, 4 weeks and at 8 weeks.
|
Headache Disability Index is used to evaluate the impact of headache on person's daily life activities.
It consists of 25 questions.
Patient answer the question as yes scored as 4, sometimes as 2 or no as 0. The score interpretation for disability is measured and for mild disability it is 10 to 28, for moderate disability is 30 to 48, for severe disability is 50 to 68 and for complete disability 72 or higher is noticed.
|
It will be measured at baseline, 4 weeks and at 8 weeks.
|
|
Plumb Line Assessment of Posture
Time Frame: It will be measured at baseline, 4 weeks and at 8 weeks.
|
A plumb line is used as reference to measure the abnormality or deviation from posture.
It helps to pinpoint those areas of the body which are away from neutral alignment of the body such as rounded shoulder, forward head posture and abnormal tilt of pelvis.
Patient reported as deviated or non deviated from neutral posture.
|
It will be measured at baseline, 4 weeks and at 8 weeks.
|
|
Cervical Flexion Rotation Test
Time Frame: It will be measured at baseline, 4 weeks and at 8 weeks.
|
Cervical flexion rotation test is used to determine the presence of joint dysfunction at the C 1/2 level.
The cervical spine is fully flexed to avoid rotational movements then rotated to right and left to find out any pain or restrictions in the joints.
Pain provocation and limited rotation indicate the positive test result.
Maximum range of rotation will be 45 which is considered as normal.
Range less than 45 will need to be corrected.
|
It will be measured at baseline, 4 weeks and at 8 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Laiba Azam, Lahore University of Biological and Applied Sciences
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 (Estimated)
January 23, 2026
Primary Completion (Estimated)
June 15, 2026
Study Completion (Estimated)
July 18, 2026
Study Registration Dates
First Submitted
December 25, 2025
First Submitted That Met QC Criteria
December 25, 2025
First Posted (Actual)
January 8, 2026
Study Record Updates
Last Update Posted (Actual)
January 26, 2026
Last Update Submitted That Met QC Criteria
January 23, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UBAS/ERB/FoRS/25/029
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.
Clinical Trials on Cervicogenic Headache
-
Meltem UzunCompletedExercise | Therapeutics | Headache, CervicogenicTurkey
-
Alabama Physical Therapy & AcupunctureUniversidad Rey Juan CarlosCompletedCervicogenic HeadachesUnited States
-
Des Moines UniversityCompleted
-
Hungarian University of Sports ScienceCairo UniversityCompleted
-
Foundation University IslamabadRecruiting
-
Cairo UniversityNot yet recruiting
-
University of LahoreCompletedCervicogenic HeadachePakistan
-
Istanbul Medipol University HospitalIstanbul Kent UniversityCompletedCervicogenic Headache | Cervicogenic HeadachesTurkey (Türkiye)
-
Ankara City Hospital BilkentRecruitingCervicogenic Headache | Third Occipital NerveTurkey (Türkiye)
-
Hong Kong Baptist UniversityActive, not recruiting
Clinical Trials on Back School Based Intervention
-
University of VigoNot yet recruitingHealthy | Low Back Pain | ExerciseSpain
-
University of Sao PauloCompletedChronic Low Back PainBrazil
-
Universitair Ziekenhuis BrusselVrije Universiteit BrusselCompletedLumbar RadiculopathyBelgium
-
Dallas VA Medical CenterAspen Medical ProductsCompletedLow Back Pain | Degenerative Disc Disease | Lumbar Spondylosis
-
Tehran University of Medical SciencesUnknown
-
Wayne State UniversityCompleted
-
Tehran University of Medical SciencesCompletedLow Back PainIran, Islamic Republic of
-
University of VigoCompletedNeck Pain | Primary Prevention | Health Education | Exercise TherapySpain
-
University of VigoCompleted
-
University of VigoCompletedNeck Pain | Health Education | Exercise TherapySpain