The aim was to investigate the effectiveness of adding aromatherapy massage with a mixture of lavender and orange oil to conventional physical therapy in individuals with chronic nonspecific low back pain on pain, central sensitization, functionality, sleep, quality of life, kinesiophobia, anxiety, and depression in this patient population.
Eligibility
Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria
* Age 18-65 years
* Chronic nonspecific low back pain ≥ 6 months
* Volunteering to participate
* Receiving treatment at physical therapy clinic
Exclusion Criteria
* History of orthopedic surgery, fracture, trauma
* Inflammatory, rheumatologic, neurological, psychiatric disorders
* Asthma
* Current psychiatric medication use
* Peripheral neuropathy or postherpetic neuralgia
* Long-term corticosteroid use
* Skin lesions/open wounds in treatment area
* Allergy to lavender, orange, or almond oil
* Positive allergic reaction to patch test
Primary outcome measure(s)
McGill Pain Questionnaire — Baseline, 4 weeks The McGill Pain Questionnaire Short Form consists of 15 items evaluating sensory and affective dimensions of pain. Each item is scored on a 0-3 Likert scale, with total scores ranging from 0 to 45. Higher scores indicate greater pain severity.
Pressure Pain Threshold (Algometer) — Baseline, 4 weeks Pressure pain threshold will be measured using an algometer to evaluate sensitivity in predefined anatomical points. The device quantifies the minimum pressure that induces pain.
Central Sensitization Inventory — Baseline and 4 weeks The Central Sensitization Inventory is a 25-item questionnaire assessing symptoms related to central sensitization. Each item is scored on a 5-point Likert scale (0-4), with total scores ranging from 0 to 100. Higher scores indicate greater central sensitization symptoms.
Trial sites (1)
Facility
City
Region
Status
Kırşehir Research and Training Hospital, Physical Therapy and Rehabilitation Clinic
Kırşehir
Merkez
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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