NCT07327827

Brief Summary

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.

Trial Health

63
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Trial Health Score

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

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet 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 Progress60%
Jan 2026Jul 2026

First Submitted

Initial submission to the registry

December 25, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

January 8, 2026

Completed
15 days until next milestone

Study Start

First participant enrolled

January 23, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 18, 2026

Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

5 months

First QC Date

December 25, 2025

Last Update Submit

January 23, 2026

Conditions

Keywords

Cervicogenic HeadacheBack School Based ProgramCranio-Cervical Muscle TrainingPainPostureHeadacheDisability

Outcome Measures

Primary Outcomes (4)

  • Visual Analogue scale

    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

    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

    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

    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.

Study Arms (2)

Back School Based Intervention

EXPERIMENTAL

Back School Based Intervention

Other: Back School Based Intervention

Cranio- Cervical Muscle Training

ACTIVE COMPARATOR

Cranio- cervical muscle Training

Other: Cranio-Cervical muscle Training

Interventions

* Patient will receive 2 sessions per week for 8 weeks for a total of 16 sessions. Each session lasted for 35 minutes. Conventional physical therapy will be same in both groups * Cranio- cervical muscle training session main focus is on the strengthening and posture correction. Cervical flexion, extension and stabilization exercises will be performed which helps to strength muscles and helps to neutralize posture and ultimately disability which is due to headache will be reduced.

Cranio- Cervical Muscle Training

* Patient will receive 2 sessions per week for 8 weeks for a total of 16 sessions. Each session lasted for 35 minutes. * Conventional Physical therapy will be provided in which stretching of the tight muscles which include SCM, upper trapezius, levator scapulae, scalene, sub occipitals, pectoralis minor, and pectoralis major. Neck stretches, chin tucks, scapular squeezes, and upper back strengthening exercises with 5 repetitions will be performed. Trigger points of sub occipitals, SCM, and temporalis are released because they cause headache. * Back School Based Intervention includes both theoretical and practical part. Patients had total of 16 sessions out of which 14 will be practical one and remaining two will be theoretical one. In theoretical part main focus is on the patient education and guidance. In practical part resistive exercises of increase intensity in each session will be performed in which main focus is on the strengthening

Back School Based Intervention

Eligibility Criteria

Age19 Years - 44 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sir Ganga Ram Hospital Lahore

Lahore, Punjab Province, 54000, Pakistan

Location

MeSH Terms

Conditions

Post-Traumatic HeadachePainHeadache

Condition Hierarchy (Ancestors)

Headache Disorders, SecondaryHeadache DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Laiba Azam

    Lahore University of Biological and Applied Sciences

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

December 25, 2025

First Posted

January 8, 2026

Study Start

January 23, 2026

Primary Completion (Estimated)

June 15, 2026

Study Completion (Estimated)

July 18, 2026

Last Updated

January 26, 2026

Record last verified: 2026-01

Locations