CGH: Efficacy of Lumbar Motor Control Training in Treatment Of Patients With Cervicogenic Headache

Sponsor

Cairo University (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT05952115

Collaborator

(none)

Enrollment

Arms

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

this study will be conducted to investigate the effect of lumbar motor control training exercise on headache frequency, duration, intensity and neck functional disability in cervicogenic headache patients

Condition or Disease	Intervention/Treatment	Phase
Cervicogenic Headache	Other: lumbar motor control exercises Other: Cervical stabilization exercises	N/A

Detailed Description

Cervicogenic Headache is a referred pain spreading from cervical structures supplied by the upper cervical spinal nerve roots (C1-C3), this referred pain that starts from the posterior aspect of the head and neck is usually found to be unilateral, and it also can spread to the frontal, temporal and orbital aspects of the head.The patient frequently reports having a terrible headache, having less neck range of motion, performing less well at work, and having trouble focusing, that may linger for hours. The convergence of primary sensory afferents from cervical nerve roots C1 to C3 with the afferents from the occiput and trigeminal nerve causes the underlying pathology. Because of this, the Suboccipital muscles particularly, which cervical roots C1 innervates to C3, are potential risk structures. Treatment options include posture correction, cervical and upper thoracic strengthening exercises, facet joint manipulation, ultrasound therapy, laser therapy, trigger release therapy, and cervical joint mobilization.famous exercise known as "Motor control exercise" attempts to improve the coordination and effectiveness of the muscles that support and govern the spine. It can also improve coordination between the deep neck flexors and superficial neck flexors and between core muscles of the lumbar region. fifty two patients will be randomly assigned to two equal groups; experimental group will receive lumbar motor control and cervical stabilization exercises and control group will receive cervical stabilization exercises only.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

52 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

lumbar motor control and cervical stabilization exerciseslumbar motor control and cervical stabilization exercises

Masking:

Double (Investigator, Outcomes Assessor)

Masking Description:

opaque sealed envelop

Primary Purpose:

Treatment

Official Title:

Efficacy of Lumbar Motor Control Training in Treatment Of Patients With Cervicogenic Headache

Anticipated Study Start Date :

Jul 16, 2023

Anticipated Primary Completion Date :

Oct 16, 2023

Anticipated Study Completion Date :

Oct 16, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: lumbar motor control exercises patients will receive lumbar motor control and cervical stabilization exercises three times a week for four weeks	Other: lumbar motor control exercises the patients will receive lumbar motor control exercises in the form of three exercises (Abdominal draw in maneuver, side-bridge, and quadruped) and the level of difficulty increased each week. For all exercises, the number of repetitions stayed the same, but the difficulty increased each week, and we progressed to the advanced level of each of the three exercises. This training achieves co-contraction of the local/deep stabilizing muscles (Transversus abdominis and multifidus) and strengthening the global/large spinal stabilizers (erector spinae and obliques). Other: Cervical stabilization exercises The exercise program consisted of an axial elongation exercise, cranio-cervical flexion exercise, cervical extension exercise, and cervical-scapulothoracic strengthening exercise. The exercise program progressed based on the exercise tolerance of the patients by increasing the repetition of the exercise (10 reps to 15 reps to 20 reps). And for the resistive exercise, the participants change to an elastic band with greater resistance (progress to the next color resistance band). Exercises were performed for 20 min/session, and an exercise log recording the date and repetition of the exercises was maintained by the therapist for each participant.
Active Comparator: cervical stabilization exercises the patients will receive cervical stabilization exercises three times a week for four weeks	Other: Cervical stabilization exercises The exercise program consisted of an axial elongation exercise, cranio-cervical flexion exercise, cervical extension exercise, and cervical-scapulothoracic strengthening exercise. The exercise program progressed based on the exercise tolerance of the patients by increasing the repetition of the exercise (10 reps to 15 reps to 20 reps). And for the resistive exercise, the participants change to an elastic band with greater resistance (progress to the next color resistance band). Exercises were performed for 20 min/session, and an exercise log recording the date and repetition of the exercises was maintained by the therapist for each participant.

Arm

Intervention/Treatment

Experimental: lumbar motor control exercises

patients will receive lumbar motor control and cervical stabilization exercises three times a week for four weeks

Other: lumbar motor control exercises

the patients will receive lumbar motor control exercises in the form of three exercises (Abdominal draw in maneuver, side-bridge, and quadruped) and the level of difficulty increased each week. For all exercises, the number of repetitions stayed the same, but the difficulty increased each week, and we progressed to the advanced level of each of the three exercises. This training achieves co-contraction of the local/deep stabilizing muscles (Transversus abdominis and multifidus) and strengthening the global/large spinal stabilizers (erector spinae and obliques).

Other: Cervical stabilization exercises

The exercise program consisted of an axial elongation exercise, cranio-cervical flexion exercise, cervical extension exercise, and cervical-scapulothoracic strengthening exercise. The exercise program progressed based on the exercise tolerance of the patients by increasing the repetition of the exercise (10 reps to 15 reps to 20 reps). And for the resistive exercise, the participants change to an elastic band with greater resistance (progress to the next color resistance band). Exercises were performed for 20 min/session, and an exercise log recording the date and repetition of the exercises was maintained by the therapist for each participant.

Active Comparator: cervical stabilization exercises

the patients will receive cervical stabilization exercises three times a week for four weeks

Other: Cervical stabilization exercises

Outcome Measures

Primary Outcome Measures

Headache frequency: [up to four weeks]
Headache frequency will measure as the number of days with headache in the last week, ranging from 0 to 7 days
Headache duration [up to four weeks]
Headache duration will measure in total hours and average number of hours headaches lasted in the past week
Headache intensity [up to four weeks]
The Visual Analog Scale will use to quantify the patient's pain level or intensity. these scale consists of line, usually 10 cm long, ranging from no pain at one end and worst pain at the other end

Secondary Outcome Measures

neck disability [up to four weeks]
Arabic version of neck disability index will be used to measure neck disability. The NDI consists of 10 sections: pain intensity, personal care, lifting, reading, headache, concentration, work, driving, sleeping, and recreation. Each section is expressed by 6 different assertions in the range 0-5, with 0 indicating no disability and 5 indicating highest disability. The total score ranges from 0 to 50.0-4= No disability,5-14= Mild disability,15-24=Moderate disability, 25-34=Sever disability,35 or more=Complete disability.

Eligibility Criteria

Criteria

Ages Eligible for Study:

20 Years to 40 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

The age of the subjects ranged from 20-40 years old, both genders.
Patients with chronic mechanical neck pain with frequent cervicogenic headaches persisting for more than 3 months.
Positive flexion rotation test.
Unilateral head pain without side shift or bilateral head pain with dominant side headache associated with neck pain and aggravated by neck movement and/or sustained awkward head positioning
Joint tenderness in at least one of the upper three cervical joints or the occipital region as detected by manual palpation.
Intensity of headache is moderate to severe.
Abnormal performance in CCFT < = 26 mmHg
Body mass index range from 18 to 25 km/m2

Exclusion Criteria:

Fracture or previous surgery on the vertebral column.
Spinal stenosis.
Disc prolapsed.
TMJ dysfunction.
Headache with autonomic involvement, dizziness, or visual disturbance.
Congenital condition of the cervical spine.
Neck pain of less than three months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Hagar Abd_El basset Ismail Marzok, principle investigator hagar Abd El basset Ismail Marzouk, Cairo University

ClinicalTrials.gov Identifier:

NCT05952115

Other Study ID Numbers:

P.T.REC/012/003835

First Posted:

Jul 19, 2023

Last Update Posted:

Jul 19, 2023

Last Verified:

Jul 1, 2023

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by Hagar Abd_El basset Ismail Marzok, principle investigator hagar Abd El basset Ismail Marzouk, Cairo University

lumbar motor control

cervicogenic hedache

cervical stabilization exercises

Additional relevant MeSH terms:

Post-Traumatic Headache

Headache

Study Results

No Results Posted as of Jul 19, 2023