Comparison of Maitland Oscillatory Mobilizations With Kaltenborn Sustained Stretch Mobilizations in Cervicogenic Headache Patients

Sponsor
Foundation University Islamabad (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05777395
Collaborator
(none)
26
1
2
5.9
4.4

Study Details

Study Description

Brief Summary

Cervicogenic headache is a common headache that causes disability and affects everyday activities. Headache related disorders are the second most common reason for years lived with disability all over the world. According to the latest International Headache Society model, cervicogenicheadache (CGH) is a secondary headache having C1-C2 dysfunction. There is marked limitation in cervical ROM specially rotation. Treatment indicated involves use of electrotherapy and thermal modalities. In addition, use of different manual therapy techniques are advocated to eliminate the root cause i.e. C1-C2 dysfunction. Maitland mobilizations for cervical spine have been found to be effective in treating CGH patients. Maitland mobilizations uses oscillatory mobilizations and has four grades. Kaltenborn, on the other hand, applies sustained stretches and has 3 grades.So, the study will be focusing on comparing the effectiveness of these two mobilizations on cervicogenic headache patients.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Maitland Oscillatory Mobilization
  • Procedure: Kaltenborn Sustained Stretch Mobilization
  • Procedure: Conventional therapy
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
26 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This is a randomized controlled trial having two groups. One group will receive conventional physical therapy along with Maitland oscillatory mobilizations and the second will receive Kaltenborn sustained stretch mobilizations with conventional physical therapy. Both groups will be recruited concurrently.This is a randomized controlled trial having two groups. One group will receive conventional physical therapy along with Maitland oscillatory mobilizations and the second will receive Kaltenborn sustained stretch mobilizations with conventional physical therapy. Both groups will be recruited concurrently.
Masking:
Single (Outcomes Assessor)
Masking Description:
The outcome assessor will not be aware of which group the participant belongs to.
Primary Purpose:
Treatment
Official Title:
Comparison of Maitland Oscillatory Mobilizations With Kaltenborn Sustained Stretch Mobilizations in Cervicogenic Headache Patients
Actual Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Jun 15, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Maitland + Conventional PT Group

Participants of this group will receive the conventional physical therapy protocol mentioned above. In addition to this, they will receive Maitland oscillatory mobilizations. 3 sets of 15 repetitions. Each set is of 30 seconds and each repetition is given in 2 seconds. Frequency: 3 times a week for 2 weeks. 6 sessions in total. Mobilizations will be performed in Grade 1 initially and then progressed to Grade 2 and 3. Techniques used are postero-anterior unilateral vertebral pressure and Maitland rotation.

Procedure: Maitland Oscillatory Mobilization
Maitland Posteroanterior unilateral vertebral pressure and Maitland cervical rotation technique will be used.3 sets of 15 repetitions. Each set is of 30 seconds and each repetition is given for 2 seconds.

Procedure: Conventional therapy
Moist heat, TENS, Neck Muscle Stretching, Neck muscle isometrics

Experimental: Kaltenborn + Conventional PT Group

Participants of this Group will receive the conventional physical therapy protocol mentioned above. In addition to this, they will receive Kaltenborn sustained stretch mobilizations. 3 sets of 15 repetitions for 3 seconds. Frequency: 3 times a week for 2 weeks. 6 sessions in total. Mobilizations will be performed in Grade 1 and then progressed to 2 and 3. Kaltenborn technique used will be atlas-axis rotation.

Procedure: Kaltenborn Sustained Stretch Mobilization
Kaltenborn sustained stretch mobilizations. 3 sets of 15 repetitions for 3 seconds. Frequency: 3 times a week for 2 weeks. 6 sessions in total. Mobilizations will be performed in Grade 1 and then progressed to 2 and 3. Kaltenborn technique used will be atlas-axis rotation

Procedure: Conventional therapy
Moist heat, TENS, Neck Muscle Stretching, Neck muscle isometrics

Outcome Measures

Primary Outcome Measures

  1. Pain intensity [2 weeks]

    Pain will be measured on the basis of Numeric Pain Rating Scale score.

  2. Cervical range of motion [2 weeks]

    Cervical rotation will be measured through CROM device

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-45 years

  • Both males and females

  • Unilateral headache with no shift of side

  • C1-C2 dysfunction

  • Headache with neck stiffness

  • Headache at least once a month in the last 3 months

  • Positive flexion rotation test (Rotation restriction is greater than 10 degrees)

  • Headache with a score of at least 4 in the Numeric pain rating scale

Exclusion Criteria:
  • Cervical spondylosis

  • Headache of non-cervical origin

  • Dizziness or visual disturbance

  • Cervical radiculopathy/ nerve root involvement/ disc herniation

  • Cervical instability/ fracture

  • Vertebrobasilar insufficiency

  • Thoracic outlet syndrome

  • Cervical spine surgery

  • Cervical spondylolisthesis

  • Spinal infection or tumors

  • Osteoporosis

  • History of trauma

  • Metabolic disorders

  • Rheumatoid Arthritis

  • Inflammatory Arthritis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fauji Foundation Hospital Rawalpindi Punjab Pakistan 4600

Sponsors and Collaborators

  • Foundation University Islamabad

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Foundation University Islamabad
ClinicalTrials.gov Identifier:
NCT05777395
Other Study ID Numbers:
  • FUI/CTR/2023/1
First Posted:
Mar 21, 2023
Last Update Posted:
Mar 21, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 21, 2023