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Cranial Electrical Stimulation In Individuals With Headache Due To Neck Pain

Effect Of Cranial Electrical Stimulation In Individuals With Cervicogenic Headache: A Quasi-Experimental Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041904
Enrollment
21
Registered
2022-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified Health Condition 2: M00-M99- Diseases of the musculoskeletal system and connective tissue Health Condition 3: M708- Other soft tissue disorders related to use, overuse and pressure

Interventions

Intervention1: CRANIAL ELECTRICAL STIMULATION: Cranial electrical stimulation was given in the â??M 5 Mode (Type- Delta Rhythm) for 20 minutes, 6days a week for 3 weeks Control Intervention1: NIL: NIL

Sponsors

Ravikant Jangra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age Between 18 to 65 Years 2 Individual with Cervicogenic Headache as diagnosed by International Study Groups criteria (CHISG) 3 Individual with unilateral head pain in occipital and upper posterior neck region 4 Individuals with NPRS Score more then 21 5 Individuals with NDI score more than 20%(10 Point on Greater )

Exclusion criteria

Exclusion criteria: 1 Individuals having headache due to migraine 2 Individuals having suffered from bilateral headache 3 Individuals having any fracture of cervical spine, osteoporosis, cervical stenosis, tumor, uncontrolled hypertension, prolonged use of steroid 4 Individuals having neurologic signs due to nerve root compression 5 Individuals with history of whiplash injury 6 weeks 6 Received any chiropractic and physiotherapy treatment within the previous month 7 Individuals with Pregnancy and breastfeeding

Design outcomes

Primary

MeasureTime frame
1. Von Korff Scale 2. Numeric Pain Rating Scale 3. Neck Disability Index 4. Pressure Algometer Timepoint: at baseline & after 3 weeks—

Secondary

MeasureTime frame
1. Von Korff Scale 2. Numeric Pain Rating Scale 3. Pressure Algometer Timepoint: baseline, at 3 weeks—

Countries

India

Contacts

Public ContactRavikant Jangra

Department of Neurological Physiotherapy,MMIPR

akankshasaxena623@mmumullana.org9958729161

Outcome results

None listed

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