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Aromatherapy Massage in Chronic Low Back Pain

The Effect of Aromatherapy Massage in Individuals With Chronic Nonspecific Low Back Pain: A Double-Blind Randomized Controlled Trial

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07578181
Enrollment
70
Registered
2026-05-11
Start date
2025-05-20
Completion date
2026-08-20
Last updated
2026-05-11

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

Conditions

Low Back Pain

Keywords

Low Back Pain, Aromatherapy, Massage

Brief summary

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.

Interventions

OTHERConventional Physiotherapy

Hotpack (10 min) TENS (20 min) Ultrasound (5 min) Stretching \& stabilization exercises (15 min) Frequency: 5 sessions/week for 4 weeks

OTHERAromatherapy Massage + Conventional Physiotherapy

Same conventional physiotherapy protocol Aromatherapy massage: Lavender + orange essential oil (%1.5 in sweet almond oil) 15 min/session 3 sessions/week for 4 weeks Massage techniques: effleurage, petrissage, friction, vibration

Sponsors

Kirsehir Ahi Evran Universitesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 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

Design outcomes

Primary

MeasureTime frameDescription
McGill Pain QuestionnaireBaseline, 4 weeksThe 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 weeksPressure 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 InventoryBaseline and 4 weeksThe 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.

Secondary

MeasureTime frameDescription
Disability (Oswestry Disability Index)Baseline and 4 weeksThe Oswestry Disability Index consists of 10 items assessing functional disability related to low back pain. Each item is scored from 0 to 5, with total scores converted into percentage disability (0-100%).
Quality of Life (SF-36)Baseline and 4 weeksThe SF-36 Health Survey evaluates quality of life across 8 domains including physical functioning, role limitations, pain, general health, vitality, social functioning, emotional role, and mental health. Scores range from 0 to 100, with higher scores indicating better health status.
Anxiety (Beck Anxiety Inventory)Baseline and 4 weeksThe Beck Anxiety Inventory is a 21-item scale measuring anxiety severity. Each item is scored from 0 to 3, with total scores ranging from 0 to 63.
Depression (Beck Depression Inventory)Baseline and 4 weeksThe Beck Depression Inventory consists of 21 items assessing depressive symptoms. Total scores classify depression severity as minimal, mild, moderate, or severe.
Kinesiophobia (Tampa Scale of Kinesiophobia)Baseline and 4 weeksThe Tampa Scale of Kinesiophobia includes 17 items rated on a 4-point Likert scale. Total scores range from 17 to 68, with higher scores indicating greater fear of movement.
Sleep Quality (Pittsburgh Sleep Quality Index)Baseline and 4 weeksThe Pittsburgh Sleep Quality Index evaluates sleep quality across 7 components. Total scores range from 0 to 21, with scores above 5 indicating poor sleep quality.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 12, 2026