Table 2.
Characteristics of the participants included in the selected studies.
| Ref. | Type of study | Subjects | |||||
|---|---|---|---|---|---|---|---|
| Total number of subjects | Mean subject age (range) | Gender (n) | Type of subject | Diagnostic systems/inclusion criteria | Baseline score for depressive symptoms | ||
| Inhalation aromatherapy | |||||||
|
| |||||||
| [18] | Placebo-controlled randomized double blind RCT | 313 | 65 (33–90) | Female (150) Male (163) |
Individuals with cancer receiving radiotherapy treatment | Patients prescribed with 8 or more fractions of radiotherapy | Baseline depression status: odds ratio of 29 using HADS. |
|
| |||||||
| [19]∗ | 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. |
|
| |||||||
| [20] | Prospective RCT | 13 | 27.3 for the control group (NA) 29.3 for the treatment 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. |
|
| |||||||
| [21] | 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. |
|
| |||||||
| [22] | 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. |
|
| |||||||
| Aromatherapy massage | |||||||
|
| |||||||
| [23] | RCT | 32 | 32.9 (23–53) in the treatment group | Female (10 in the treatment group) Male (4 in the treatment group) No information provided on the number of female and male subjects in the control 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. |
|
| |||||||
| [24] | 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. |
|
| |||||||
| [25] | 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). |
|
| |||||||
| [26] | Nonblinded randomized crossover trial | 16 | 46.1 (37.9–54.3) | Female (15), male (1) |
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. |
|
| |||||||
| [19]∗ | 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. |
|
| |||||||
| [27] | 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. |
|
| |||||||
| [28] | 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. |
|
| |||||||
| [29] | 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.