| Literature DB >> 28133489 |
Dalinda Isabel Sánchez-Vidaña1, Shirley Pui-Ching Ngai1, Wanjia He1, Jason Ka-Wing Chow1, Benson Wui-Man Lau1, Hector Wing-Hong Tsang1.
Abstract
Background. Depression is one of the greatest health concerns affecting 350 million people globally. Aromatherapy is a popular CAM intervention chosen by people with depression. Due to the growing popularity of aromatherapy for alleviating depressive symptoms, in-depth evaluation of the evidence-based clinical efficacy of aromatherapy is urgently needed. Purpose. This systematic review aims to provide an analysis of the clinical evidence on the efficacy of aromatherapy for depressive symptoms on any type of patients. Methods. A systematic database search was carried out using predefined search terms in 5 databases: AMED, CINHAL, CCRCT, MEDLINE, and PsycINFO. Outcome measures included scales measuring depressive symptoms levels. Results. Twelve randomized controlled trials were included and two administration methods for the aromatherapy intervention including inhaled aromatherapy (5 studies) and massage aromatherapy (7 studies) were identified. Seven studies showed improvement in depressive symptoms. Limitations. The quality of half of the studies included is low, and the administration protocols among the studies varied considerably. Different assessment tools were also employed among the studies. Conclusions. Aromatherapy showed potential to be used as an effective therapeutic option for the relief of depressive symptoms in a wide variety of subjects. Particularly, aromatherapy massage showed to have more beneficial effects than inhalation aromatherapy.Entities:
Year: 2017 PMID: 28133489 PMCID: PMC5241490 DOI: 10.1155/2017/5869315
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.629
Search terms and database search strategy.
| ID | Disease search terms |
|---|---|
| 1 | Depress |
| 2 | Major depress |
| 3 | Mood disorder |
| 4 | Depressive disorder |
| 5 | 1 OR 2 OR 3 OR 4 |
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| ID | RCT search terms |
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| 6 | Controlled clinical trial |
| 7 | Random |
| 8 | 6 OR 7 |
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| ID | Aromatherapy search terms |
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| 9 | Aroma |
| 10 | Aromatherapy |
| 11 | Aromatic therapy |
| 12 | Essential oil |
| 13 | Fragrance |
| 14 | Fragrant oil |
| 15 | Scent |
| 16 | Massage therapy |
| 17 | Medical massage |
| 18 | Massage |
| 19 | 9 OR 10 OR 11 OR 12 OR 13 OR 14 OR 15 OR 16 OR 17 OR 18 |
| 20 | 5 AND 8 AND 19 |
Truncation symbol for database search.
Figure 1Study selection flowchart.
Characteristics of the participants included in the selected studies.
| Ref. | Type of study | Subjects | |||||
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| Total number of subjects | Mean subject age (range) | Gender ( | Type of subject | Diagnostic systems/inclusion criteria | Baseline score for depressive symptoms | ||
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| [ | Placebo-controlled randomized double blind RCT | 313 | 65 (33–90) | Female (150) | Individuals with cancer receiving radiotherapy treatment | Patients prescribed with 8 or more fractions of radiotherapy | Baseline depression status: odds ratio of 29 using HADS. |
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| [ | Randomized observational pilot study with repeated measures | 28 | 32 (25–43) | Female (28) | Postpartum women | 0–18-month postpartum women with scores of 10 or higher on either the Edinburgh Postnatal Depression Scale or the Generalized Anxiety Disorder Scale | The baseline score using the Edinburgh Postnatal Depression Scale for the control group was 15.9 and 16.1 for the intervention group. |
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| [ | Prospective RCT | 13 | 27.3 for the control group (NA) | Female (13) | Pregnant women | 28-week-pregnant women, singleton pregnancy | Depression-dejection scale baseline score using POMS was 2.7 in the control group and 1.6 in the treatment group. |
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| [ | Randomized controlled crossover study | 20 | 20.5 | Female (20) | College students | Healthy volunteers | The depression-dejection scale baseline score using POMS was not provided, but the change difference between pre- and posttreatment was reported. The change in depression-dejection score was lower than −1 in the treatment group and statistically significant when compared to the change in the control group. |
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| [ | Controlled double-blinded RCT | 320 | 20–30, average age NA | Female (320) | Pregnant women | Women between 18–35 years, with a pregnancy age between 38 and 42 weeks, a score of 12 or less in the Edinburgh test | Depression grade baseline in the Edinburgh test was 6.3 in the control group and 6.1 in the intervention group. |
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| [ | RCT | 32 | 32.9 (23–53) in the treatment group | Female (10 in the treatment group) | Patients with depression and/or anxiety | Patients scoring more than 7 in the Montgomery-Asberg Depression Rating Scale and/or the Tyrer Brief Anxiety Scale | The baseline using the Montgomery-Asberg Depression Rating Scale was 19.8 in the control group and 30 in the treatment group. The baseline using the HADS was 14.6 and 15.3 in the control and treatment group, respectively. |
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| [ | Double blind RCT | 42 | 73, (44–85) | Female (32), male (10) | Individuals with cancer | Individuals with cancer with a wide variety of levels of physical and psychological symptoms | Baseline score using HADS was not stated. Only the median change in HADS was provided being 0 for the aromatherapy group, −1.5 for the massage group, −0.5 for the aromatherapy massage group, and 0.5 for the control. |
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| [ | RCT | 288 | 52.1; 52.8 for the usual care group; and 51.5 for the usual care plus aromatherapy group | Female (250), male (38) | Individuals with cancer | Patients diagnosed with cancer, a prognosis of more than 3 months, with clinical anxiety or depression | The baseline score using the Center for Epidemiological Studies Depression Scale was 26.1 for the aromatherapy group and 26 for the group receiving usual care (control). |
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| [ | Nonblinded randomized crossover trial | 16 | 46.1 (37.9–54.3) | Female (15), | Patients diagnosed with idiopathic environmental intolerance | Clinical examination by a physician and scoring above 26 for men and 30 for women in the Chemical Odor Sensitivity Scale | Depression subscale baseline score using POMS was around 2.8 in the control period. |
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| [ | Randomized observational pilot study with repeated measures | 28 | NA | Female (28) | Postpartum women | 0–18-month postpartum women with scores of 10 or higher on either the Edinburgh Postnatal Depression Scale or the Generalized Anxiety Disorder Scale | The baseline score using the Edinburgh Postnatal Depression Scale for the control group was 15.9 and 16.1 for the intervention group. |
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| [ | Single blind RCT | 39 | 52.5; 51.1 for the aromatherapy group; and 54 for the cognitive behavior therapy group | Female (31), male (8) | Individuals with cancer | Patients diagnosed for at least one month, who also had at least a predicted survival of 6 months and score 11 or more in the HADS for anxiety or depression | The baseline score in the depression-dejection subscale of POMS was 11.2 for the aromatherapy massage group and 13.4 for the control group. |
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| [ | RCT | 90 | 53.70 for the control group (49.42–57.98), 52 (47.12–56.88) for the massage therapy group, and 53.35 (49.01–57.69) | Female (90) | Women who entered their menopausal period naturally | Woman, age between 45 and 60 years, with amenorrhea for at least 1 year | At baseline, according to the Menopause Rating Scale, the frequency of the severity of the depressive mood was reported as mild (14.9%), moderate (36.8%), severe (20.7%), and very severe (2.3%). No difference was found among the groups at baseline. |
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| [ | RCT | 25 | 34–48, average age NA | Female (25) | Women with children | Women whose children were diagnosed with attention deficit hyperactivity disorder | Baseline using the Beck Depression Inventory was 8.6 in the control group and 10.8 in the treatment group. |
In this study, both aromatherapy modalities were tested, inhalation aromatherapy and aromatherapy massage. Therefore, the study was included in both categories in the table. NA, not available; HADS, Hospital Anxiety and Depression Scale; POMS, Profile of Mood States.
Description of the interventions and protocols used in the selected studies.
| Reference | Intervention and protocol | |||||||
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| Comparison group ( | Treatment group(s) ( | Type of essential oil used | Duration of the study | Administration method | Treatment frequency | Duration per session | Total number of sessions | |
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| [ | Control with sweet almond cold-pressed pure vegetable oil with no fragrance (NA) | (i) Carrier oil with fractionated low (NA) grade essential oil | (i) Fractionated oils of unknown purity diluted 1 : 3 in carrier oil | 8 weeks | 3 drops of oil applied to a bib worn during the administration of the treatment | Daily | 15–20 min | 56 |
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| [ | Control, jojoba oil (14) | (i) 2% dilution of a mixture of essential oils (6) | (i) 0.25 rose otto essential oil and 0.75 lavender, 2% dilution of the essential oil mixture | 4 weeks | 8 drops of oil applied to a cotton pad. Subjects were instructed to smell the cotton pad for 15 min | Twice a week | 15 min | 8 |
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| [ | Control, no intervention (6) | (i) Pure essential oil (7) | (i) Lavender | 1 day | 5 drops of oil applied on a filter placed in a diffuser | Once | 5 min | 1 |
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| [ | Control, water (20) | (i) Pure essential oil (20) | (i) Yuzu | 2 days | 10 | Twice | 10 min (sessions separated in intervals around 2.6 days) | 2 |
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| [ | Control group which did not receive any nonpharmacological method for pain relief of labor (160) | (i) Nonpharmacological methods for pain relief of labor including showering, being in upright position, aromatherapy, and soft music without words (160) | (i) 20% lavender essential oil | During labor | 10 × 10 cm cloth impregnated with 1 mL 20% lavender essential oil which was attached to the mother's breast at the beginning of the active phase. The aromatherapy intervention was combined with other nonpharmacological interventions | Once | Duration of the active phase of labor | 1 |
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| [ | Control, grape seed oil (16) | (i) Diluted essential oil (16) | (i) 9 essential oils (bergamot, lemon clary sage, lavender, roman chamomile, geranium, rose otto, sandalwood, and jasmine). A combination of essential oils chosen by the aromatherapist on each treatment session (16) | 12 weeks | 15 mL grape seed carrier oil with (4 drops) or without essential oils applied in a full body massage using gentle effleurage and petrissage | Once a fortnight | 40 min | 6 |
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| [ | Control, no intervention (13) | (i) Aromatherapy massage (16) | (i) 1% lavender essential oil diluted in sweet almond oil | 2 years | Back massage | Weekly | 30 min | 4 |
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| [ | Usual supportive care | (i) Usual supportive care and aromatherapy massage | (i) 20 essential oils | 10 weeks | Standardized massage agreed by the therapists | Weekly | 1 h | 4 |
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| [ | Control, no intervention | (i) Aromatherapy massage | (i) 1% massage oil containing melissa, juniper, and rosemary essential oils mixed into jojoba oil (1 : 2 : 2 ratio) | 8 weeks | Standardized massage on the back, shoulders, arms, hands, lower legs, and feet using 20–30 mL massage oil | Every two weeks | 1 h | 4 |
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| [ | Control, essential oil blend unscented white lotion (14) | (i) 2% dilution of a mixture of essential oils (8) | (i) 0.25 rose otto essential oil and 0.75 lavender, 2% dilution of the essential oil mixture | 4 weeks | Topic application of the oil or lotion on both hands with gentle strokes of homogeneous pressure and speed | Twice a week | 15 min | 8 |
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| [ | Cognitive behavior therapy (19) | (i) Aromatherapy massage (20) | (i) 20 essential oils | 2 years | Standardized massage combined with treatment as usual (routine support) | Weekly | 1 h | Up to 8 sessions in 10 weeks |
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| [ | Control, no intervention (30) | (i) Aromatherapy massage (30) | (i) 3% oil mixture containing lavender, geranium, rose, and rosemary (4 : 2 : 1 : 1 ratio) in almond and evening primrose oil | 4 weeks | Massage in the abdomen, tights, and arms using massage oil containing essential oils or odorless liquid petrolatum. Massage was applied with clockwise circular movements and light pressure | Twice a week | 30 min | 8 |
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| [ | Control, no intervention (12) | (i) Aromatherapy massage (13) | (i) Jojoba oil containing 2% lavender and 2% geranium essential oils | 4 weeks | Massage on the neck, shoulders, arms, back, and legs including effleurage, friction, petrissage, and vibration at a moderate pressure using 20 mL of massage oil | Twice per week | 40 min | 8 |
In this study, both aromatherapy modalities were tested, inhalation aromatherapy and aromatherapy massage. Therefore, the study was included in both categories in the table. NA, not available; min, minutes; h, hour.
Description of the measurement tools, outcomes, and conclusions.
| Reference | Outcome measures | ||||
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| Scale | Comparison group | Intervention group(s) | Outcome | Improvement of depressive symptoms | |
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| [ | (i) HADS | Control group | (i) Carrier oil with fractionated low grade essential oil | Increased outcome measurement when compared to the baseline (18%–22% in HADS) using multivariate analysis. No statistically significant difference observed. | No |
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| [ | (i) EPDS | Control group | (i) 2% dilution of a mixture of essential oils | The mean difference in EPDS scores between the control group and the intervention group at end point was −3.981 but no statistically significant difference was observed. Combined analysis of inhalation aromatherapy and massage aromatherapy showed statistically significant difference with a mean difference of −4.8. | Yes |
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| [ | (i) POMS | No intervention | (i) Pure essential oil | Depression-dejection subscale scores before and after test were 2.7 and 1.2 in the comparison group and 1.6 and 0.6 in the intervention group, respectively. No statistically significant difference was observed. | No |
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| [ | (i) POMS in TMD | Control group | (i) Pure essential oil | Change in TMD score was 0.5 ± 2.2 in the control group and −1.28 ± 2.6 in the intervention group (statistically significant difference). | Yes |
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| [ | (i) EPDS | No intervention | (i) Nonpharmacological methods for pain relief of labor including showering, being in upright position, aromatherapy, and soft music without words | Depression grades (0–30) before and after delivery were 6.3 and 8.8 in the no intervention group and 6.1 and 7.8 in the intervention group, respectively. No statistically significant difference was observed. | No |
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| [ | (i) MADRS | Control group | (i) Diluted essential oil | The scores in the MADRS at baseline and end point were 19.8 and 21.1 in the control group and 30 and 18.1 in the treatment group. Statistically significant difference was observed between the test and control group. | Yes |
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| [ | (i) HADS | No intervention | (i) Aromatherapy massage | The median change in HADS at baseline and end point was 0.5 in the no intervention group, 0 in the aromatherapy massage group, and −1.5 in the massage group. No statistically significant difference among the groups. | No |
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| [ | (i) CES-D | Active control (usual supportive care) | (i) Usual supportive care and aromatherapy massage | The scores using CES-D at baseline and end point were 26.0 and 4.6 in the active control group and 25.9 and 6.2 in the intervention group, respectively. No statistically significant difference observed between the 2 groups. | No |
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| [ | (i) POMS | No intervention | (i) Aromatherapy massage | Statistically significant difference between the 2 groups when comparing the pre- and postsessions in all the POMS subscales including depression-dejection. | Yes |
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| [ | (i) EPDS | Control group | (i) m'technique (hand massage) | The mean difference between the baseline and end point using EPDS was −6.031. | Yes |
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| [ | (i) POMS-TMS | Active control (cognitive behavior therapy) | (i) Aromatherapy massage | The POMS-TMS decreased in both groups after intervention from 46.3 to 26.5 in the active control group and 44.5 to 29 in the intervention group. | Yes |
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| [ | (i) MRS | No intervention | (i) Aromatherapy massage | The mean difference in psychological symptoms (including depressive mood) was −0.379 in the no intervention group (no statistically significant difference), −3.49 in the aromatherapy massage group (statistically significant difference), and −1.20 in the massage group (statistically significant difference). | Yes |
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| [ | (i) BDI | No intervention | (i) Aromatherapy massage | The BDI score before and after test was 8.6 and 8.5 in the control group and 10.8 and 6.5 in the intervention group (statistically significant difference). | Yes |
In this study, both aromatherapy modalities were tested, inhalation aromatherapy and aromatherapy massage. Therefore, the study was included in both categories in the table. CES-D, Center of Epidemiological Studies Depression (self-reported depression); BDI, Beck Depression Inventory; DSM-IV, modified Diagnostic and Statistical Manual of Mental Disorder criteria; EPDS, Edinburgh Postnatal Depression Scale; HADS, Hospital Anxiety and Depression Scale; MADRS, Montgomery-Asberg Depression Rating Scale; MRS, Menopause Rating Scale; POMS, Profile of Mood States; TMD, Total Mood Disturbance; TMS, Total Mood Score (shortened version of the profile of mood states).
Quality assessment of studies included according to the Jadad scale.
| Reference | Quality assessment of methodology based on Jadad scale | |||||||
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| Randomization | Appropriate method of randomization and description | Blinding | Description of dropouts/withdrawals | Jadad score (score out of 5) | ||||
| No blinding | Single blind | Double blind | Appropriate method of double blinding and description | |||||
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| [ | Yes | Yes | No | No | Yes | Yes | No | 4 |
| [ | Yes | No | Yes | No | No | NA | Yes | 2 |
| [ | Yes | Yes | Yes | No | No | NA | Yes | 3 |
| [ | Yes | No | No | Yes | No | No | No | 1 |
| [ | Yes | Yes | No | No | Yes | No | Yes | 4 |
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| [ | Yes | No | Yes | No | No | NA | No | 1 |
| [ | Yes | Yes | No | No | Yes | Yes | Yes | 5 |
| [ | Yes | Yes | No | No | Yes | No | Yes | 3 |
| [ | Yes | Yes | Yes | No | No | NA | NA | 2 |
| [ | Yes | No | Yes | No | No | NA | Yes | 2 |
| [ | Yes | Yes | No | Yes | No | No | Yes | 3 |
| [ | Yes | Yes | Yes | No | No | No | No | 2 |
| [ | Yes | No | Yes | No | No | NA | No | 1 |
In this study, both aromatherapy modalities were tested, inhalation aromatherapy and aromatherapy massage. Therefore, the study was included in both categories in the table. NA, not applicable.