Actively Recruiting
Osteopathic Manipulative Treatment vs Physiotherapy in Cervicocranial Dysfunction
Led by Burim Peli · Updated on 2026-04-29
50
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to compare the effects of osteopathic manipulative treatment and standard physiotherapy in patients with cervicocranial dysfunction. The study will evaluate outcomes including dizziness, headache impact, neck disability, and psychological stress. Participants will be randomly assigned to one of two groups: osteopathic treatment or standard physiotherapy. The interventions will be applied over a defined treatment period, and outcomes will be measured before and after the intervention. The purpose of this study is to determine which approach is more effective in improving symptoms and functional outcomes in patients with cervicocranial dysfunction.
CONDITIONS
Official Title
Osteopathic Manipulative Treatment vs Physiotherapy in Cervicocranial Dysfunction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 65 years
- Cervicocranial symptoms present for at least three months
- Neck pain with or without headache
- Dizziness linked to neck movement or position
- Clinical diagnosis of cervicocranial dysfunction
- Ability to understand and complete study questionnaires
- Willingness to participate and provide informed consent
You will not qualify if you...
- Diagnosed vestibular disorders
- Central neurological disorders affecting dizziness or balance
- Recent severe cervical spine trauma
- History of cervical spine surgery
- Systemic inflammatory diseases or serious spinal conditions
- Red flags related to cervical spine found during screening
- Current participation in intensive physiotherapy or rehabilitation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Imperium Medical Clinic
Pristina, Pejton, Kosovo, 30000
Actively Recruiting
Research Team
B
Burim Peli, Phd cand.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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