Low Back Pain Clinical Trial
Official title:
The Effects of Massage With Frankincense and Myrrh Oil in Treating Chronic Low Back Pain: A Randomized Controlled Trial
NCT number | NCT04494165 |
Other study ID # | 2019/460 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 1, 2019 |
Est. completion date | November 5, 2019 |
Verified date | July 2020 |
Source | TC Erciyes University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This randomized controlled study was conducted to determine the effect of massage with
frankincense and myrrh oil in treating chronic low back pain.
A total of 91 individuals over the age of 18 who agreed to participate in the study, who had
no verbal communication problems, and who had complaints of low back pain for at least the
past three months were included in the study. In this research, 3x2 (experiment, control and
plasebo group x pre-test post-test) split plot design was used The data were collected using
the data sheet, Visual Analogue Scale (VAS), Aberdeen Low Back Pain Scale (ALBPS) and
Roland-Morris Disability Scale (RMDS). Standard treatment was applied to all three groups for
three weeks, every weekday. In addition to the standard treatment, 2 sessions of waist
massage per week were applied to the aromatherapy Group with frankincense and myyrh essential
oil and to the Placebo Group with jojoba fixed oil in accordance with the aromatherapy
protocol. Massage was not applied to the control group.
In the results of working, the decrease in RMDS (p <0.001), ALBPS (p <0.001) and VAS (p
<0.001) scores of the aromatherapy group was found to be statistically higher than the other
two groups.
As a result, aromatherapy massage with Fankincense and Myyrh essential oil can be added to
traditional treatments as an easy-to-apply complementary health application with no
significant side effects to relieve pain and reduce disability in an individual's daily life
in chronic low back pain patient care.
Status | Completed |
Enrollment | 91 |
Est. completion date | November 5, 2019 |
Est. primary completion date | November 5, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients over the age of 18, - who agreed to participate in the study, - who had no communication problems (hearing, vision, speech, perception problem) - who had been suffering from (chronic) low back pain for at least the past three months were included in the study. Exclusion Criteria: - Patients with allergic skin reactions, - those who had undergone a surgical operation or fracture in the lumbar region in the last year, - those with a fever above 38.5 °C, - those undergoing a neurological rehabilitation, - patients with active infections such as tuberculosis and AIDS, - those undergoing cancer treatment, - those who had received massage therapy for the last three months were excluded from the study. |
Country | Name | City | State |
---|---|---|---|
Turkey | Ülkü Özdemir | Kayseri |
Lead Sponsor | Collaborator |
---|---|
TC Erciyes University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analogue Scale | It is stated that VAS is more sensitive and reliable than other one-dimensional scales in the measurement of pain intensity(*). In their study, Cline, Herman, Show et al. (1992) have reported that vertical use of VAS is better understood by patients. (*). It was used in our study to assess the severity of low back pain. It is a-10 cm ruler with endpoints of "no pain" at one end and "unbearable pain" at the other end. The scale was explained to the patient and they were asked to mark any place between these two points that matched the severity of their pain. The distance between the beginning of "no pain" and the point marked by the patient was measured and recorded in centimeters. | three weeks | |
Primary | Aberdeen Low Back Pain Scale | It is a scale that patients can fill out by themselves to decide on the health status of patients with low back pain. It is a 19-item scale consisting of questions about number of days with pain, use of painkillers, factors that increase and decrease pain, pain areas, sensory change, loss of strength/weakness, lumbar flexion, difficulty falling asleep due to pain, sitting, getting up, walking, work/daily activities, sex life, leisure activities, self-care, and days spent in bed. The total score of the scale adapted to Turkish by Ilhanli et al. ranges between 0 and 100, and the high score indicates more severe low back pain. Its Cronbach's Alpha value was indicated as 0.88 (*). In our study, the power of the scale was 100%. | three weeks | |
Primary | Roland-Morris Disability Scale | The patient is asked to mark the appropriate ones among the 24 cases specified in this form. RMDS consists of 24 expressions based on the patient's perception of low back pain and associated disability. These items are indicated as physical activity (15), sleep/rest (3), psychosocial (2), household management (2), eating (1) and frequency of pain (1) (*).This test is based on measuring how low back pain affects the patient's activities of daily living. Yes responses are calculated as "1", no responses as "0" points, and a total score between 0 and 24 is obtained. Higher score means more disability. The Turkish validity study of the scale was conducted by Küçükdeveci et al. Cronbach's alpha value of the scale was indicated as 0.85-0.89 (*). In our study, the power of the scale was 100% | three weeks |
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