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Recruiting NCT07725198

Immediate Neuromuscular Responses of the Obliquus Capitis Inferior Following Upper Cervical Manual Therapy

No phase Interventional Head and Neck Headache

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Thrust long-axis manipulation of C1-C2.
Who it may be relevant to
Registry conditions: Head and Neck, Headache. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study used a prospective, randomized, repeated-measures experimental design to investigate the immediate effects of two upper cervical manual therapy interventions on craniovertebral angle (CVA), clinician-perceived atlas position, and musculoskeletal ultrasound-derived obliquus capitis inferior (OCI) muscle morphology

Interventions

  • Other Thrust long-axis manipulation of C1-C2
    One thrust manipulation is provided in the thrust group. a 5 second long axis hold traction of C1-C2 was repeated 3 times in the mobilization group

Primary outcome measures

  • MSK Ultrasound [Time frame: before intervention, immediately after, and 24 hours after intervention]
Secondary outcome measures (2)
  • Atlas position [Time frame: before intervention, immediately after, and 24 hours after intervention]
  • Craniovertebral angle [Time frame: before intervention, immediately after, and 24 hours after intervention]

Eligibility criteria

Inclusion criteria

  • read and understand English
  • no previous history of cervical spine surgery or traumatic cervical injury
  • no contraindications to cervical manual therapy

Exclusion criteria

  • any absolute contraindications to cervical manipulation
  • any other medical condition considered unsafe for manual therapy.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Florida Gulf Coast University Marieb Hall 101 — Fort Myers

Identifiers

NCT: NCT07725198 · 2025-11

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗