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Craniosacral therapy for quality of life improvement in patients with cervical pain

THE IMPACT OF CRANIOSACRAL THERAPY ON THE QUALITY OF LIFE OF PATIENTS WITH CERVICAL PAIN - PROSPECTIVE CONTROLLED EXPERIMENTAL STUDY - NIL

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104457
Enrollment
50
Registered
2026-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

None listed

Interventions

Intervention1: physiotherapy and craniosacral therapy: experimental group will receive 12 therapy sessions (3 session/week) of physiotherapy and craniosacral therapy, with a total duration of 4 weeks

Sponsors

Osteokinetomedica
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: age between 35 and 55 years; presence of cervical pain; absence of major associated comorbidities; attendance of at least 85% of the scheduled therapy sessions; absence of current pharmacological treatment; and no acute medical conditions.

Exclusion criteria

Exclusion criteria: fibromyalgia, spinal tumors, prior cervical spine surgery, significant cervical trauma (e.g., whiplash injuries or cervical fractures), infections, and inflammatory rheumatic diseases.

Design outcomes

Primary

MeasureTime frame
This study aims to highlight the role of Cranio-Sacral Therapy in achieving faster pain reduction, thereby influencing stress levels and improving the quality of life of patients with cervical pain.Timepoint: baseline and at 4 weeks—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

Romania

Contacts

Public ContactAnca Maria Oltean

University of Oradea

dciobanu@uoradea.ro0722839150

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026