A study to compare the effects of Eye Cervical Re-Education Program (ECRP) with Conventional Treatment in Cervicogenic Headache patients.

Comparing the efficacy of Eye Cervical Re-Education Program (ECRP) with Conventional Therapy in Cervicogenic Headache patients: A Comparative study - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/076143

Enrollment

Registered

2024-11-01

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M530- Cervicocranial syndrome

Interventions

Intervention1: Eye Cervical Re-Education Program: 1. Hot pack - 15 minutes 2. IFT - 15 minutes ECRP includes 10 exercises: The patient will be placed in the supine position, with the physiotherapist s

Eligibility

Inclusion criteria

Inclusion criteria: A. Diagnosed Cervicogenic headache patients as per Internation Headache Society under International Criteria for Headache Disorders - 3. B. Patients who can understand and read spoken English.

Exclusion criteria

Exclusion criteria: A. Patients with other primary headaches (Migraine, Tension-type Headache). B. Patients exhibiting any red flags (i.e., tumor, fracture, metabolic diseases, rheumatoid arthritis, osteoporosis, resting blood pressure greater than 140/90 mmHg, prolonged history of steroid use, etc.). C. A diagnosis of cervical spinal stenosis. D. Patients having a known history of musculoskeletal soft tissue injury or surgery in the last 6 months. E. History of congenital musculoskeletal/neurological disorders such as epiphyseal plate disturbance, and multiple sclerosis. F. History of any psychological disorders such as seizures, or schizophrenia.

Design outcomes

Primary

Measure	Time frame
Cervical Joint Position Error - Active movement angle reproduction test in which the difference between the reference point position and the position produced by the subject is called Joint Position Error. 2. Cervical Range of Motion 3. Verbal rating Scale 4. Headache Disability IndexTimepoint: Baseline values will be taken before the start of the treatment, and post-treatment values will be taken after the completion of the treatment, that is, after a period of four weeks, after the patient has taken 12 sessions of the treatment.	—

Measure

Time frame

Cervical Joint Position Error - Active movement angle reproduction test in which the difference between the reference point position and the position produced by the subject is called Joint Position Error. 2. Cervical Range of Motion 3. Verbal rating Scale 4. Headache Disability IndexTimepoint: Baseline values will be taken before the start of the treatment, and post-treatment values will be taken after the completion of the treatment, that is, after a period of four weeks, after the patient has taken 12 sessions of the treatment.

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Secondary

Measure	Time frame
Cervical Range of Motion - Flexion, extension, left and right rotations, left and right lateral flexionTimepoint: Baseline values will be taken before the start of the treatment, and post-treatment values will be taken after the completion of the treatment, that is, after a period of four weeks, after the patient has taken 12 sessions of the treatment.	—

Countries

India

Contacts

Public ContactRadhika Sinha

Amar Jyoti Institute of Physiotherapy

prernasaxena.88@gmail.com9999456988

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026