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THE IMPACT OF CRANIOSACRAL THERAPY ON THE QUALITY OF LIFE IN PATIENTS WITH CERVICAL PAIN

THE IMPACT OF CRANIOSACRAL THERAPY ON THE QUALITY OF LIFE IN PATIENTS WITH CERVICAL PAIN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240722062512N2
Enrollment
30
Registered
2025-03-30
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

non-specific cervical pain. Myalgia

Interventions

Intervention 1: Intervention group: The intervention group received 12 sessions of craniosacral therapy, 3 times/week, each session lasting 1 hour and consisting of mild and gentle pressure on the sku

Sponsors

University of Oradea
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patients with non-specific cervical pain- Aged between 35-55 years old No major acute or associated pathologies Agreement of participation in the study 85% of attendance to the therapeutical sessions Treatment continuity No current pain medication- Complete assessment sessions

Exclusion criteria

Exclusion criteria: Patients with acute cervical pain Major acute or associated pathologies Disagreement of participation in the study Less than 85% of attendance to the therapeutic sessions Discontinuity of treatment Current pain medication Incomplete assessment

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: We ill use a Health related quality of life questionnaire - it is a self administered questionnaire.

Secondary

MeasureTime frame
The second outcome is intensity of pain. Timepoint: one assessment before intervention and final assessment after 4 weeks. Method of measurement: VAS scale.

Countries

Romania

Contacts

Public ContactAnca Maria Dragan

University of Oradea

ancamariadragan@yahoo.com+40 259 418 105

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026