Skip to main content
Wiley Open Access Collection logoLink to Wiley Open Access Collection
. 2025 Jan 6;24(1):e16775. doi: 10.1111/jocd.16775

Exploring Complementary and Alternative Medicine Use for the Management of Acne Vulgaris Among University Students: Forms, Trends, and Information Sources

Sari Taha 1,2,, Manal Taha 3, Sa'ed H Zyoud 4,5,6
PMCID: PMC11701388  PMID: 39757764

ABSTRACT

Background

Acne vulgaris is a common skin disease that has physical and psychological impacts. Patients diagnosed with acne often use complementary and alternative medicine, despite the insufficient evidence.

Aims

This cross‐sectional study sought to identify the types, trends in and reasons for utilizing complementary and alternative medicine for acne among university students.

Patients/Methods

The study was conducted among health sciences students from March to June, 2023, using clinical examination and a questionnaire. All participants were assessed for a diagnosis of acne.

Results

The final sample size consisted of 367 participants, of whom 68.9% were females and 31.1% were males. The study revealed a high prevalence of acne (74.4%). Among those with acne, 59.7% reported using complementary and alternative medicine, with the biological forms being most frequent at 90.2%. The reasons commonly stated for using complementary and alternative medicine were lack of severity (48.5%) and the potential for internet‐based self‐treatment (33.1%). The main sources of information were the internet (44.8%) and social media (41.1%). Age, gender, and the occurrence of acne on the chin were associated with complementary and alternative medicine use (p < 0.05).

Conclusions

The use of complementary and alternative medicine for treating acne is widespread, with a tendency toward biological forms. Healthcare practitioners should be familiar with the patterns of complementary and alternative medicine use for the treatment of acne to better meet patient needs and concerns. Policymaking can leverage the role of online resources in addressing the use of unconventional treatment modalities.

Keywords: acne, acne vulgaris, community health, complementary and alternative medicine, dermatology, university students


Abbreviations

AV

acne vulgaris

BMI

body mass index

CAM

complementary and alternative medicine

DALY

disability‐adjusted life year

WHO

World Health Organization

1. Introduction

Acne vulgaris (AV) is a chronic inflammatory disease of the skin, especially in areas of rich sebaceous gland distribution. Dermatological manifestations may range from mild skin lesions, such as comedones, to severe forms of cysts and nodules, with potential long‐term scarring and pigmentation [1, 2, 3]. Moreover, AV is associated with several psychological comorbidities, such as anxiety, low self‐esteem, and body dysmorphic syndrome [4, 5, 6, 7]. Hormonal imbalance, the proinflammatory effect of Propionibacterium acnes , oxidant–antioxidant imbalance, and increased sebum production, and proinflammatory lipids have been implicated in the pathophysiology of AV [3, 8, 9]. The choice of treatment, including oral and topical medications, depends on the severity of AV, and patients' and physicians' preferences [10]. The burden of AV is high and continues to rise over time. In 2019, the global prevalence and the disability‐adjusted life years (DALYs) of acne were estimated at 231.2 million and 5 million, respectively [11]. Particularly, AV is a disease of adolescents and young adults, as almost 85% of these populations are affected globally [12].

Complementary and alternative medicine (CAM) has been defined differently but mostly refers to similar sets of practices. According to the MSD manual, CAM is defined as “the healing approaches and therapies that historically have not been included in conventional, mainstream Western medicine.” [13] The application of scientific criteria to test CAM practices has been challenged by methodological difficulties, including the inherent unfeasibility of standardizing treatments and outcomes, and the difficulty of blinding and designing case–control groups [14].

The use of various forms of CAM in the treatment of acne has been investigated in multiple studies, which have reported inconclusive evidence [15, 16, 17, 18, 19]. However, the use of some forms of CAM may lead to allergic, mechanical, infectious, and nutritional complications [20]. Different factors may influence patients' decision to initiate and continue using CAM in different areas, including dissatisfaction with, and failure of, conventional medicine, belief in therapeutic effectiveness, and interest in a holistic approach to health [21, 22, 23, 24].

While studies have used different definitions of CAM, its use among AV patients ranges from 52.4% to 77% [25, 26, 27, 28, 29, 30]. Some CAM practices are common regardless of the region, while others are unique to certain areas, such as the use of a locally prepared cleanser in Nigeria [31]. The commonly used CAM methods to treat AV in the Eastern Mediterranean Region (EMR) include honey, yogurt, lemon, clay, vinegar, oatmeal, in addition to other herbs and nutritional supplements [25, 28, 30, 31].

The prevalence of CAM use among Palestinians ranges between 45.9% and 91.5%. While some studies have focused on the use of herbal remedies, others have addressed CAM use among certain populations, including people with coronary heart disease, diabetes mellitus, hypertension, pediatric patients, cancer, hemodialysis, and pregnant women [32, 33, 34, 35]. However, research addressing acne in Palestine is scarce. To the best of the authors' knowledge, no research has explored the use of CAM in the management of AV in Palestine.

Patients with AV may delay or refrain from seeking medical opinion and opt for self‐medication for various reasons, including the preference for natural approaches, perceived effectiveness, and easy accessibility [26, 27, 29]. The delay in seeking medical opinion may lead to chronic complications such as scarring [2]. Similarly, some alternative treatment methods may sometime lead to adverse outcomes [20]. Therefore, exploring the forms and patterns of CAM use in the management of AV in Palestine is key to evaluating the scope of the problem and informing potential interventions. This study aimed to explore the forms of CAM utilized to manage AV and the factors influencing their utilization among university students. It also aimed to identify the patterns related to CAM use, including the reasons and sources of information related to this use.

2. Methods

2.1. Study Design

This was a cross‐sectional study based on a self‐administered questionnaire. It was conducted from March to June 2023 at the Faculty of Medicine and Health Sciences, An‐Najah National University (NNU) in Nablus, Palestine.

2.2. Population and Sampling

All students registered in the second semester of 2022/2023 at the Faculty of Medicine and Health Sciences, An‐Najah National University, were eligible for inclusion. Based on information obtained from the faculty administration, the population (N) of students enrolled was 5100 students, the vast majority of whom were studying medicine. To determine the minimum sample size (X), a desired margin of error (E) was set at 5%; a confidence level of 95% (the corresponding z value is 1.96); and the expected prevalence (P) of AV was 80.9% in a previous survey conducted among medical students at NNU [36]. The following two equations were used to determine the initial sample size (n) and to correct for a finite population (N):

n=N/1+NE2
X=n/1+n/N

The minimum sample size was estimated at approximately 346, but the sample size was increased to 427 to account for nonresponse and missing data. Convenience sampling was utilized to invite students to participate because obtaining records of students for randomization of sampling was infeasible.

2.3. Data Collection Tool and Variables

All participants were assessed for acne under clear daylight by a certified physician. Each participant filled a paper‐based, self‐administered questionnaire without interaction with other participants and in front of the researcher. The questionnaire was developed by the authors in Arabic, the native language of the students. A pilot study was carried out on 25 respondents to ensure the clarity and cultural acceptability of the questionnaire. Based on the feedback, the structure and content were modified, and additional suggestions were added to the CAM list. The final questionnaire consists of three sections.

The first section gathered information on demographic characteristics, including age; gender; university major; year of study; and self‐reported weight and height to measure BMI. The World Health Organization's (WHO) BMI classification was adopted (underweight: < 18.5 kg/m2, normal weight: 18.5–24.9 kg/m2, overweight: 25.0–29.9 kg/m2, obese: > 30.0 kg/m2) [37, 38].

The second section contains clinical questions on receiving dermatologist‐prescribed treatment for AV; first‐degree family history of AV (yes, no); duration of AV (< 1 year, 1–5 years, 5–10 years, > 10 years); location of AV (forehead, right cheek, left cheek; nose; chin; and trunk); and smoking status (current, defined as daily smoking during the past year; previous, quit smoking with the specified rate > 1 year ago; or nonsmoker).

The third section contains questions that explore the use and pattern of complementary and alternative medicine. The first part of this section explored the types and forms of CAM used to manage AV and was developed by the authors based on the consultation and cross‐review of pharmacological professors who are experts in CAM, especially those forms that are used locally. Similar studies were reviewed to create a comprehensive list of regional and global CAM. The MSD Manual list of CAM was employed as a framework to assign CAM forms to the following types: biological (including animal‐ and plant‐based modalities of CAM, diet therapy, vitamins and supplements, oily products and chelation therapy); mind–body medicine (relaxation, meditation, hypnotherapy, and biofeedback‐guided imagery); whole medical systems (Ayurveda, homeopathy, naturopathy Chinese medicine, prophetic medicine, including ruqyah); manipulative and body‐based practices (hijama, massage, reflexology, and chiropractic); and energy medicine (acupuncture, magnets, therapeutic touch, Reiki) [39]. Hijama is a religion‐based cupping therapy that is purported to remove “stagnant blood and toxins” [40]. Most of the biological CAM therapies listed are topically applied and not orally consumed (Table 4). The second part of this section explored the patterns of CAM use, including the reasons for using CAM, sources of information, response to CAM use, and side effects associated with CAM use.

TABLE 4.

Forms of complementary and alternative medicine.

CAM name n (%)
Blossom water* 58 (35.6%)
Yogurt* 47 (28.8%)
Aloe vera * 46 (28.2%)
Honey* 44 (27.0%)
Massage 34 (20.9%)
Rice water* 28 (17.2%)
Relaxation 26 (16.0%)
Lime* 25 (15.3%)
Meditation 19 (11.7%)
Only Vitamin C 19 (11.7%)
Multivitamins 19 (11.7%)
Hijama (wet cupping) 16 (9.8%)
Oily products* 14 (8.6%)
Turmeric* 14 (8.6%)
Prophetic medicine 13 (8.0%)
Yoga 13 (8.0%)
Cinnamon* 13 (8.0%)
Egg* 12 (7.4%)
Yeast* 11 (6.7%)
Tea* 09 (5.5%)
Low carb diet 09 (5.5%)
Mint* 08 (4.9%)
Parsley* 08 (4.9%)
Vinegar* 07 (4.3%)
Rosemary* 06 (3.7%)
Only vitamin B12 06 (3.7%)
Oats* 05 (3.1%)
Only vitamin E 04 (2.5%)
Chinese medicine 03 (1.8%)
Intermittent fasting diet 03 (1.8%)
Orange* 02 (1.8%)
Georgina* 02 (1.2%)
Keto diet 01 (0.6%)
Dead sea mask* 01 (0.6%)

Note: Percentages are not mutually exclusive due to the potential multiplicity of responses and thus sum up to more than 100%. Vitamins were listed separately when consumed without other vitamins and as ‘multivitamins’ when consumed as part of a multivitamin‐containing product.

*

These CAM modalities are topically applied and not orally consumed.

2.4. Data Analysis

The Statistical Package for Social Sciences program version 25 (SPSS) was used to insert and analyze the data, employing descriptive and inferential statistics. The mean (±SD) was reported for age, and percentages and frequencies were reported for categorical and ordinal variables. Percentages for potential multiple‐response variables, including acne locations, professional treatment modalities, CAM types and forms, reasons for use, sources of information, and side effects are not mutually exclusive and sum to more than 100%. The chi‐squared test was used to explore the association between the use of CAM (binary variable) and the following variables: age (categorized into 18–19, 20–21, ≥ 22 years old), gender, university major, year of study, BMI, smoking status (binary, with a smoker defined as smoking cigarettes/vape/shisha during the last 30 days [41]), family history, duration, bodily location of acne, and the use of professional treatment. Fisher's exact test was used when the assumptions of the chi‐squared test were violated. Significance was determined using a threshold p < 0.05.

2.5. Ethical Considerations

Permission was obtained from the IRB office at An‐Najah National University. The purposes and nature of the research study were communicated clearly to the respondents before obtaining informed consent. The privacy and confidentiality of the participants were ensured in regard to clinical information and collected data.

3. Results

Of the 427 students approached, 19 declined to complete the questionnaire (4.4%), and 41 were excluded from the study due to missing data (9.6%). The variables with negligible percentages of missing data were BMI (0.04%) and smoking status (0.03%). The study included a final sample of 367 participants, with 253 females (62.7%), 114 males (37.3%), and a mean age of 20.5 years (SD ± 1.54). Two‐thirds of the respondents were studying medicine (67.6%), followed by dentistry (6.8%), nursing (6.0%), and pharmacy (3.5%). Slightly below a third of the respondents were second‐year students (29.4%), followed by first‐year (24.5%), fourth‐year (16.6%), and third‐year students (15.8%). Table 1 shows the demographic characteristics of the participants in more detail.

TABLE 1.

The demographic characteristics of the respondents.

Variable n (%)
Age (years)
18–19 116 (31.6%)
20–21 135 (36.8%)
 22 116 (31.6%)
Gender
Male 114 (31.1%)
Female 253 (68.9%)
BMI a
Underweight 32 (8.7%)
Healthy range 237 (64.6%)
Overweight 67 (18.3%)
Obese 15 (4.1%)
Study major
Medicine 248 (67.6%)
Dentistry 25 (6.8%)
Nursing 22 (6%)
Pharmacy 13 (3.5%)
Medical imaging 12 (3.3%)
Physiotherapy 9 (2.5%)
Anesthesia and resuscitation 8 (2.2%)
Speech pathology 8 (2.2%)
Pharmacy doctor 6 (1.6%)
Medical laboratory sciences 4 (1.1%)
Midwifery 4 (1.1%)
Optometry 4 (1.1%)
Cardiac perfusion technology 3 (0.8%)
Cosmetics and skin care 1 (0.2%)
Year of study
First year 90 (24.5%)
Second year 108 (29.4%)
Third year 58 (15.8%)
Fourth year 61 (16.6%)
Fifth year 43 (11.7%)
Sixth year 7 (1.9)
Acne history
Yes 273 (74.4%)
No 94 (25.6%)
Smoking status a
Current smoker 48 (13.1%)
Previous smoker 4 (1.1%)
Nonsmoker 303 (82.6%)

Note: The total values percentages of three variables (study major, year of study, and smoking status) sums up to either 100.1% or 99.9% due to rounding percentages to the nearest 0.01.

Abbreviations: AV, acne vulgaris; BMI, body mass index.

a

Frequency (percentages) of missing values: BMI 16 (4.3%); and 12 smoking status (3.3%).

The prevalence of AV was 74.4%, with 72.2% reporting having a family history. Of the 273 participants with AV, only 39.2% used a treatment modality prescribed by a dermatologist. The forehead was the most common area of acne (62.2%), followed by the left cheek (53.1%), right cheek (51.6%), chin (35.6%), trunk (27.4%), and nose (14.7%). For the duration of the disease, 41.0% had acne for < 1 year, 47.6% for one to 5 years, 9.5% for 5–10 years, and 1.8% for > 10 years. Table 2 includes further detail on the AV‐related clinical characteristics of respondents, and Table 3 lists the medications utilized as per professional advice.

TABLE 2.

Association between the demographic and clinical characteristics of the respondents with acne vulgaris and the use of complementary and alternative medicine.

Variable CAM use; n (%) Total n a p
Yes No
Age (years)
18–19 62 (72.1%) 24 (27.9%) 86 (31.5%) 0.010*
20–21 56 (57.7%) 41 (42.3%) 97 (35.5%)
 22 45 (50.0%) 45 (50.0%) 90 (33.0%)
Gender
Male 28 (36.8%) 48 (63.2%) 76 (27.8%) < 0.001*
Female 135 (68.5%) 62 (31.5%) 197 (72.2%)
BMI b
Underweight 21 (80.8%) 5 (19.2%) 26 (10.0%) 0.08
Healthy range 104 (59.1%) 72 (40.9%) 176 (68.0%)
Overweight 24 (53.3%) 21 (46.7%) 45 (17.4%)
Obese 9 (75.0%) 3 (25.0%) 12 (4.6%)
Family history of AV
Yes 115 (58.4%) 82 (41.6%) 197 (72.2%) 0.47
No 48 (63.2%) 28 (36.8%) 76 (27.8%)
Study major
Medicine 97 (53.9%) 83 (46.1%) 180 (65.9%) 0.22
Dentistry 11 (68.8%) 5 (31.3%) 16 (5.8%)
Nursing 14 (82.4%) 3 (17.6%) 17 (6.2%)
Pharmacy 8 (72.7%) 3 (27.3%) 11 (4.0%)
Medical imaging 6 (54.5%) 5 (45.5%) 11 (4.0%)
Physiotherapy 5 (62.5%) 3 (37.5%) 8 (2.9%)
Anesthesia and resuscitation 7 (100.0%) 0 (0.0%) 7 (2.5%)
Speech pathology 3 (60.0%) 2 (40.0%) 5 (1.8%)
Pharmacy doctor 3 (75.0%) 1 (25.0%) 4 (1.5%)
Medical laboratory sciences 3 (75.0%) 1 (25.0%) 4 (1.5%)
Midwifery 3 (75.0%) 1 (25.0%) 4 (1.5%)
Optometry 1 (33.3%) 2 (66.7%) 3 (1.1%)
Cardiac perfusion technology 1 (50.0%) 1 (50.0%) 2 (0.7%)
Cosmetics and skin Care 1 (100.0%) 0 (0.0%) 1 (0.3%)
Year of study
First year 49 (74.2%) 17 (25.8%) 66 (24.1%) 0.08
Second year 43 (74.2%) 31 (41.9%) 74 (27.1%)
Third year 23 (50.0%) 23 (50.0%) 46 (16.8%)
Fourth year 25 (55.6%) 20 (44.4%) 45 (16.4%)
Fifth year 18 (51.4%) 17 (48.6%) 35 (12.8%)
Sixth 05 (71.4%) 02 (28.6%) 07 (2.6%)
Duration of acne
Less than a year 73 (65.2%) 39 (34.8%) 112 (41.0%) 0.41
1–5 years 74 (56.9%) 56 (43.1%) 130 (47.6%)
5–10 years 13 (50.0%) 13 (50.0%) 26 (9.5%)
> 10 years 3 (60.0%) 2 (40.0%) 5 (1.8%)
Location of acne
Forehead 99 (58.2%) 71 (41.8%) 170 (62.2%) 0.52
Right cheek 85 (60.3%) 56 (39.7%) 141 (51.6%) 0.90
Left cheek 83 (57.2%) 62 (42.8%) 145 (53.1%) 0.33
Nose 20 (50.0%) 20 (50.0%) 40 (14.7%) 0.16
Chin 66 (68.0%) 31 (32.0%) 97 (35.6%) 0.04*
Trunk 51 (68.0%) 24 (32.0%) 75 (27.4%) 0.09
Professional treatment
Yes 67 (62.6%) 40 (37.4%) 107 (39.2%) 0.43
No 96 (57.8%) 70 (42.2%) 166 (60.8%)
Smoking status
Yes 22 (53.7%) 19 (46.3%) 41 (15.0%) 0.39
No 141 (60.8%) 91 (39.2%) 232 (85.0%)

Note: The chi‐squared test was used to test the association between the use of complementary and alternative medicine and other variables. Fisher's exact test was used when the assumptions of the chi‐squared test were violated. Percentages of the locations of acne vulgaris are not mutually exclusive due to potential multiplicity of response and thus sum up to more than 100%. The total values percentages of some variables might sum up to either more or less than 100% due to rounding percentages to the nearest 0.01.

Abbreviations: AV, acne vulgaris; BMI, body mass index.

a

The total count is the frequency of respondents with acne (n = 273).

b

Frequency (percentages) of missing values: BMI 14 (5.1%).

*

p value is below the threshold value for significance (0.05).

TABLE 3.

Drugs used in cases which sought professional dermatological care.

Name of drug n (%)
Facial cleanser 82 (76.6%)
Isotretinoin (PO) 52 (48.6%)
Medical cream 46 (43.0%)
Medical soap 37 (34.6%)
Adapalene and benzoyl peroxide (TOP) 4 (3.7%)
Benzoyl peroxide alone (TOP) 3 (2.8%)
Clindamycin (TOP) 3 (2.8%)
Doxycycline (PO) 3 (2.8%)
Erythromycin and Adapalene (TOP) 1 (0.9%)
Azithromycin (PO) 1 (0.9%)
Benzoyl peroxide and lipo‐hydroxy acid (TOP) 1 (0.9%)
Clindamycin and adapalene (TOP) 1 (0.9%)
Corticosteroid cream 1 (0.9%)
Fucidin (TOP) 1 (0.9%)
Salicylic acid (TOP) 1 (0.9%)
Betamethasone and Gentamicin (TOP) 1 (0.9%)

Note: Percentages are not mutually exclusive due to the potential multiplicity of responses and thus sum up to more than 100%.

Abbreviations: PO, per os (oral); TOP, topical.

Among those with AV, 59.7% were CAM users. Biological CAM forms were used by 90.2%, followed by mind–body practices (34.4%), physical practices (30.1%), and whole medical systems (9.8%). The most common CAM used were topically applied blossom water (by 35.6% of cases), yogurt (28.8%), aloe vera (28.4%), honey (28.2%), massage (20.9%), and rice water (17.2%), and relaxation (16.0%), lime (15.3%), meditation (11.7%), vitamin C (11.7%), multivitamins (11.0%), and hijama (9.8%). Table 4 lists the forms of CAM utilized by the respondents.

The most frequently reported reasons for using CAM were the perception that AV was not severe enough to seek professional advice (48.5%); self‐searching for treatment on the internet (33.1%); CAM was suggested by someone's recommendation (26.4%); CAM was easier to reach than professional treatment (15.3%); and the patient had no time to seek professional advice (13.5%). The most common sources of information on CAM use were the internet (44.8%), social media (41.1%), family (34.4%), friends (26.4%), healthcare professionals (20.2%), and commercials (8.6%). Table 5 shows the reasons and sources of information in more detail.

TABLE 5.

The reasons for using complementary and alternative medicine and the source of information.

Pattern of CAM use n (%)
Reasons that prompted patient to use CAM as a treatment
Acne was not severe enough to seek professional advice 79 (48.5%)
Self‐exploration for a treatment on the internet 54 (33.1%)
Recommendations made by others 43 (26.4%)
CAM was easier to reach than medical treatment 25 (15.3%)
Limited time to seek professional advice 22 (13.5%)
Pharmacist's recommendation to use CAM 19 (11.7%)
CAM is safer compared to conventional treatment 18 (11.0%)
CAM method was effective when used previously 13 (8.0%)
High cost of conventional treatment 12 (7.4%)
Embarrassed to seek medical advice 5 (3.1%)
Failure of conventional treatment 0 (0.0%)
Source of information of using CAM
Internet 73 (44.8%)
Social media 67 (41.1%)
Family 56 (34.4%)
Friends 43 (26.4%)
Healthcare professional 33 (20.2%)
Commercials 14 (8.6%)
Books and magazines 9 (5.5%)
Other people (not a family member or a friend) 5 (3.1%)
TV 2 (1.2%)
Articles 2 (1.2%)

Note: Percentages are not mutually exclusive due to the potential multiplicity of responses and thus sum up to more than 100%.

Less than half of CAM users reported some benefit from using CAM (43.5%), and slightly over a third reported no effect (38.0%), while only an insignificant minority said their acne worsened after using CAM (0.01%). The most common side effects of CAM were dehydration (30.7%), erythema (28.2%), desquamation (24.5%), skin itching (14.1%), eye itching (6.7%), eye redness (6.7%), and skin discoloration (4.9%). Table 6 shows the reported responses to CAM and side effects in more detail.

TABLE 6.

Results of using complementary and alternative medicine.

Pattern of CAM use n (%)
The response to using CAM
Better effect 71 (43.5%)
Worse effect 03 (0.01%)
No effect 62 (38.0%)
Side effects of CAM
Dehydration 50 (30.7%)
Erythema 46 (28.2%)
Desquamation 40 (24.5%)
Skin itching 23 (14.1%)
Eye itching 11 (6.7%)
Eye redness 11 (6.7%)
Skin discoloration 8 (4.9%)
Swelling 7 (4.3%)
Nail changes 4 (2.5%)
Hair changes 4 (2.5%)
Ulcers 4 (2.5%)
Fever 3 (1.8%)
Scaling 1 (0.6%)

Note: Percentages are not mutually exclusive due to the potential multiplicity of responses and thus sum up to more than 100%.

Only age (p = 0.010), gender (p < 0.001), and having acne on the chin (p = 0.04) were significantly associated with using CAM. Data analysis did not reveal any significant association between using CAM and any other demographic and clinical variables, including university major (p = 0.01), year of study (p = 0.08), BMI (p = 0.08), smoking status (p = 0.39), family history of acne (p = 0.47), duration of acne (p = 0.418), receiving dermatologist‐prescribed treatment (p = 0.44), and all other body locations of acne (p > 0.05). Table 2 displays the associations in more detail.

4. Discussion

The use of unconventional treatment methods in the management of AV may be laden with serious complications. To the best of the authors' knowledge, this was the first study to explore the use of CAM in the management of AV in Palestine. The study used a self‐administered questionnaire to identify the methods of CAM used to manage AV and the factors influencing their use among students in health‐related sciences. This study revealed a high prevalence of AV among the respondents, who used a variety of CAM forms, especially biologically based preparations, for various reasons. This use was associated with gender, age, and having acne on the chin. The most commonly cited sources of information to use CAM were the internet, social media, and family.

This study revealed that the prevalence of AV was 74.4%. In comparison with other studies among similar age groups, the prevalence reported by this study is higher than that in China (51.3%), Saudi Arabia (56.2%), France (60.7%), and Turkey (65.4%) [28, 42, 43, 44] but lower than that in Brazil and another study in Saudi Arabia [29, 45]. The global prevalence of AV varies widely, particularly across age groups, with the highest incidence in adolescence [46]. Variability in the prevalence of AV among young adults can be attributed to differences in nutritional habits and methodology, including demographic characteristics of populations, sample size, and data collection tools [46, 47, 48]. For instance, AV can be self‐reported or diagnosed by a clinician, potentially leading to over‐ or underestimation of the actual prevalence.

Most of the participants who have AV used at least one form of CAM (59.7%), with most using biological CAM. The popularity of CAM among diverse patient populations in Palestine can be ascribed to the influence of culture and religion. These traditional healing practices, rooted in Palestinian culture and transmitted across generations, embody a holistic and proactive approach to well‐being that promotes the use of CAM. Moreover, religious beliefs not only encourage the use of spiritual practices but also promote nonspiritual methods, such as herbs and other botanical remedies, as mentioned frequently in religious texts [49, 50].

However, the prevalence of CAM utilization among university students with AV is lower than the rates reported in most local studies involving other populations, including pregnant women, pediatric patients, and patients with hypertension and cancer [32, 33, 34, 35, 51]. This discrepancy might be attributed to differences in the clinical and demographic characteristics of the study population. Pregnant women, for example, are more inclined to comply with professional advice that emphasizes the intake of vitamins and minerals and discourages the use of herbs, aligning with pregnancy‐specific safety concerns [34]. Furthermore, patients with hypertension and cancer tend to be older than university students and are thus more inclined toward traditional medicine [32, 51]. In parallel, a study that investigated CAM use among university students, who have similar characteristics to the current study population, revealed reasonable use of CAM compared with older populations [52]. Moreover, students studying health‐related majors may be less likely to use CAM because of the knowledge, awareness, and culture emphasizing adherence to conventional biomedicine.

In comparison with global studies conducted among patients with AV, the rate of CAM use in this study is comparable to findings from two studies in Turkey (56.9% and 64.3%) [27, 28] but lower than those reported in three other studies in Turkey (74.41%), Saudi Arabia (77%), and South Korea (87.4%) [25, 30, 53]. This variation may have arisen from differences in methodology; for instance, one study included facial cleansers, medical soaps, and medical creams within the definition of CAM, although these are regularly prescribed by dermatologists as part of the treatment regimen [53].

The most frequently used type of CAM in this study was biological, with topically applied blossom water, yogurt, aloe vera, honey, massage, and rice water identified as the most common forms. Some of these animal‐ or plant‐based products are also used regionally to varying degrees to manage AV. Similar to the present study, honey, yogurt, and lemon were the most commonly used CAM in Saudi Arabia [25, 26], while herbs, lime, clay, blossom water, and vinegar were more commonly used in Turkey [27, 30]. The prevailing CAM methods used for AV were substantially different in other global regions. In South Korea, one study reported that cosmetics, diet therapy, and cleansing and bathing techniques were most common [53]. In Nigeria, a locally made cleanser, Dudu Osun, was commonly used [31]. The increasing variation in CAM forms with the movement from similar ethnocultural to regional and global settings highlights the impact of culture and religion on the pattern of CAM use. In Palestine, certain biological CAM, such as herbs and honey, are commonly used among the most studied populations, as these are rooted in inherited cultural practices and encouraged by religious texts. On the other hand, energy‐based practices and whole therapeutic systems, such as Chinese medicine and Reiki, are unpopular and thus rarely used, except for religion‐based practices such as prophetic medicine and hujama, as revealed by this study. Moreover, blossom water and aloe vera, which were commonly reported in the present study, are components of many over‐the‐counter acne preparations worldwide. Research into the efficacy of aloe vera in treating skin conditions has been undertaken, but more extensive research is still needed [54, 55].

The most reported reasons for using CAM in this study were the perception that AV was not severe enough to seek medical opinion, the influence of the internet and people, and the convenience associated with using CAM. This is unlike other regional studies in which reasons for using CAM were related to the ineffectiveness of medical therapy, recurrence reduction, affordability, and safety [30, 56]. Only in one other study did the lack of severity encourage the participants to self‐medicate, although not necessarily with CAM [26]. Given that most cases of AV in the present study were mild, patients might have found it cumbersome to seek medical opinion, especially in an environment conducive to using CAM. The relative inconvenience associated with seeking medical opinion might also be attributed to the loaded appointment schedule and shortage of Palestinian dermatologists, with 1.13 dermatologists per 100 000 individuals [57].

In this study, the internet and social media were the most cited sources of information regarding CAM, replacing traditional influencers, such as family and friends, followed by healthcare professionals. Similarly, the internet was the major source of information in other studies conducted among AV patients in South Korea and Turkey [30, 53], while family and friends were still the main influencers in Saudi Arabia [56]. The growing influence of social media and the digital world on health‐seeking behavior [58], especially on the use of unorthodox medicine, underscores the need for tailored interventions to address this trend and ensure access to reliable information, especially among females who were found to significantly use more CAM. Moreover, patients may turn to digital resources when CAM is not discussed in clinical settings. Integrating CAM knowledge into the medical education and clinical practice of medical students and physicians, along with encouraging discussions about CAM in clinical settings, is key for improving care quality and ensuring patient safety. Notably, specialty programs around the world have been increasingly adopting CAM‐integrated curricula in their continuous medical education [59, 60, 61, 62].

This study showed that gender and age are significantly associated with CAM. The gender association is consistent with other regional studies involving AV patients [25, 26, 27, 30, 56]. This might be explained by the gender roles of females as more involved in skincare and beauty practices [63]. Likewise, global studies have demonstrated that females are more inclined to resort to CAM use in general, which was shown to be affected by social factors such as income level [64, 65, 66]. Contrary to our study, the age association was not reported in other studies conducted among wider age groups, limiting comparison with this study [25, 27, 30]. Only one study reported such an association among university students, but it focused on over‐the‐counter medications [26]. Of note, seeking a professional opinion was not associated with CAM use in the present study. This is in contrast to a Korean study where AV patients who sought a medical opinion were significantly less likely to use traditional medicine [67]. This contrast may indicate healthcare workers' reluctance to discuss CAM in local dermatology practice, which further stresses the need to design interventions targeting healthcare workers and incorporating CAM into clinical practice.

5. Strengths and Limitations

This is the first study to measure the prevalence of AV in among Palestinian young adults, who are a typical age group affected by AV. This helps reflects the scale of the problem and forms the basis for further research to evaluate the economic burden of AV and guide healthcare resource allocation and health policy planning. However, this study may exhibit measurement bias for several reasons. First, the utilization of self‐reported questionnaires for data collection introduces the potential for reporting bias and recall bias. Respondents might have provided dishonest responses due to social desirability concerns. They might have also been unaware of certain CAM products, particularly those that are prepared by others or commercially manufactured. Moreover, the compilation of CAM practices in the survey may not encompass the full spectrum of these practices, as the selection is profoundly influenced by cultural factors. Although respondents were given the opportunity to supplement the provided list with unlisted CAM methods, the ability to do so was constrained by difficulties in recalling and comprehending the defining characteristics of CAM methods. In addition, the reported side effects were not matched to a CAM form or period of CAM use. Moreover, specific types of CAM, such as biological options, were more commonly used by the participants than other types, such as whole medical system, limiting generalizability to certain types of CAM. Finally, the study reliance on a nonprobability convenience sampling technique and its exclusive focus on data collection within a single university context limit its generalizability. As such, caution must be exercised when extrapolating the findings to the broader population of Palestinian university students.

6. Conclusions

AV is a prevalent dermatological disease that may lead to chronic scarring and psychological comorbidity. The use of CAM to manage AV is common despite the inconclusive evidence. This study aimed to investigate the use of CAM in the management of AV, including the forms and patterns of CAM use and the factors influencing this usage. The majority of university students used CAM, which was associated with age and gender. Most used biological forms of CAM due to reasons related to lack of severity, self‐exploration on the internet, and the influence of others. The internet and social media, followed by family and friends, were the most common sources of information. Interventions should address the emerging influence of the internet and social media on the use of unconventional treatment modalities, especially among females. Moreover, CAM should be integrated into medical education and clinical practice of physicians to address possible CAM use among AV patients and its potential consequences.

Author Contributions

S.T. performed the literature search, collected and analyzed the data, and drafted the manuscript. M.T. was responsible for the integrity of the data and results, participated in the writing of the manuscript and data analysis, and provided critical input to improve the intellectual content of the study. S.T. and S.H.Z. established the concept and design, supervised the survey team, led the data analysis, and contributed to the final writing of the manuscript. All authors read and accepted the final manuscript.

Ethics Statement

The Institutional Review Board (IRB) of An‐Najah National University approved this study. They issued the appropriate permission documents for it. The students were free to accept or reject the invitation to participate in the study voluntarily. Verbal informed consent was obtained from each subject who agreed to participate in this study. The confidentiality of the data was ensured. The IRB of An‐Najah National University approved only verbal informed consent. The reason for verbal informed consent is that participants were only required for the interview and were not subjected to any harm as long as their privacy was kept confidential. The authors confirmed that all the methods were performed following the relevant guidelines and regulations.

Conflicts of Interest

The authors declare no conflicts of interest.

Funding: The authors received no specific funding for this work.

Data Availability Statement

Data collected and analyzed for this study are available from the corresponding author upon reasonable request.

References

  • 1. Jeremy A. H., Holland D. B., Roberts S. G., Thomson K. F., and Cunliffe W. J., “Inflammatory Events Are Involved in Acne Lesion Initiation,” Journal of Investigative Dermatology 121, no. 1 (2003): 20–27. [DOI] [PubMed] [Google Scholar]
  • 2. Holland D. B., Jeremy A. H., Roberts S. G., Seukeran D. C., Layton A. M., and Cunliffe W. J., “Inflammation in Acne Scarring: A Comparison of the Responses in Lesions From Patients Prone and Not Prone to Scar,” British Journal of Dermatology 150, no. 1 (2004): 72–81. [DOI] [PubMed] [Google Scholar]
  • 3. Bellew S., Thiboutot D., and Del Rosso J. Q., “Pathogenesis of Acne Vulgaris: What's New, What's Interesting and What May Be Clinically Relevant,” Journal of Drugs in Dermatology 10, no. 6 (2011): 582–585. [PubMed] [Google Scholar]
  • 4. Golchai J., Khani S. H., Heidarzadeh A., Eshkevari S. S., Alizade N., and Eftekhari H., “Comparison of Anxiety and Depression in Patients With Acne Vulgaris and Healthy Individuals,” Indian Journal of Dermatology 55, no. 4 (2010): 352–354. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Saitta P., Keehan P., Yousif J., Way B. V., Grekin S., and Brancaccio R., “An Update on the Presence of Psychiatric Comorbidities in Acne Patients, Part 1: Overview of Prevalence,” Cutis 88, no. 1 (2011): 33–40. [PubMed] [Google Scholar]
  • 6. Akinboro A. O., Ezejiofor O. I., Olanrewaju F. O., et al., “The Impact of Acne and Facial Post‐Inflammatory Hyperpigmentation on Quality of Life and Self‐Esteem of Newly Admitted Nigerian Undergraduates,” Clinical, Cosmetic and Investigational Dermatology 11 (2018): 245–252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Marron S. E., Miranda‐Sivelo A., Tomas‐Aragones L., et al., “Body Dysmorphic Disorder in Patients With Acne: A Multicentre Study,” Journal of the European Academy of Dermatology and Venereology 34, no. 2 (2020): 370–376. [DOI] [PubMed] [Google Scholar]
  • 8. Zouboulis C. C., “Acne and Sebaceous Gland Function,” Clinics in Dermatology 22, no. 5 (2004): 360–366. [DOI] [PubMed] [Google Scholar]
  • 9. Borzyszkowska D., Niedzielska M., Kozlowski M., et al., “Evaluation of Hormonal Factors in Acne Vulgaris and the Course of Acne Vulgaris Treatment With Contraceptive‐Based Therapies in Young Adult Women,” Cells 11, no. 24 (2022): 4078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Zaenglein A. L., Pathy A. L., Schlosser B. J., et al., “Guidelines of Care for the Management of Acne Vulgaris,” Journal of the American Academy of Dermatology 74, no. 5 (2016): 945–973. [DOI] [PubMed] [Google Scholar]
  • 11. Chen H., Zhang T. C., Yin X. L., Man J. Y., Yang X. R., and Lu M., “Magnitude and Temporal Trend of Acne Vulgaris Burden in 204 Countries and Territories From 1990 to 2019: An Analysis From the Global Burden of Disease Study 2019,” British Journal of Dermatology 186, no. 4 (2022): 673–683. [DOI] [PubMed] [Google Scholar]
  • 12. Institute for Health M, Evaluation , GBD Compare Data Visualization (Seattle: IHME, University of Washington, 2020). [Google Scholar]
  • 13.“Overview of Integrative, Complementary, and Alternative Medicine,” https://www.msdmanuals.com/professional/special‐subjects/integrative‐complementary‐and‐alternative‐medicine/overview‐of‐integrative‐complementary‐and‐alternative‐medicine.
  • 14. Millstine D., Overview of Integrative, Complementary, and Alternative Medicine (Rahway, NJ, USA: MSD Manual Professional Edition, 2022). [Google Scholar]
  • 15. Cao H., Yang G., Wang Y., et al., “Complementary Therapies for Acne Vulgaris,” Cochrane Database of Systematic Reviews 1, no. 1 (2015): CD009436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Jones V. A., Patel P. M., Wilson C., Wang H., and Ashack K. A., “Complementary and Alternative Medicine Treatments for Common Skin Diseases: A Systematic Review and Meta‐Analysis,” JAAD International 2 (2021): 76–93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Nwabudike L. C., “Individualised Homeopathic Treatment of Acne‐An Analysis of 83 Patients,” Homeopathy 110, no. 4 (2021): 271–276. [DOI] [PubMed] [Google Scholar]
  • 18. Rai S., Gupta G. N., Singh S., et al., “Efficacy of Individualized Homeopathic Medicines in Treatment of Acne Vulgaris: A Double‐Blind, Randomized, Placebo‐Controlled Trial,” Homeopathy 111, no. 4 (2022): 240–251. [DOI] [PubMed] [Google Scholar]
  • 19. Lalla J. K., Nandedkar S. Y., Paranjape M. H., and Talreja N. B., “Clinical Trials of Ayurvedic Formulations in the Treatment of Acne Vulgaris,” Journal of Ethnopharmacology 78, no. 1 (2001): 99–102. [DOI] [PubMed] [Google Scholar]
  • 20. Niggemann B. and Gruber C., “Side‐Effects of Complementary and Alternative Medicine,” Allergy 58, no. 8 (2003): 707–716. [DOI] [PubMed] [Google Scholar]
  • 21. Luff D. and Thomas K. J., “Getting Somewhere', Feeling Cared for: Patients' Perspectives on Complementary Therapies in the NHS,” Complementary Therapies in Medicine 8, no. 4 (2000): 253–259. [DOI] [PubMed] [Google Scholar]
  • 22. Sirois F. M. and Gick M. L., “An Investigation of the Health Beliefs and Motivations of Complementary Medicine Clients,” Social Science & Medicine 55, no. 6 (2002): 1025–1037. [DOI] [PubMed] [Google Scholar]
  • 23. McFadden K. L., Hernandez T. D., and Ito T. A., “Attitudes Toward Complementary and Alternative Medicine Influence Its Use,” Explorer 6, no. 6 (2010): 380–388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Thanner M., Nagel E., and Loss J., “Complementary and Alternative Medicine in the German Outpatient Setting: Extent, Structure and Reasons for Provision,” Gesundheitswesen 76, no. 11 (2014): 715–721. [DOI] [PubMed] [Google Scholar]
  • 25. Ahmad A., Alghanemi L., Alrefaie S., Alorabi S., Ahmad G., and Zimmo S., “The Use of Complementary Medicine Among Acne Valguris Patients: Cross Sectional Study,” Journal of Dermatology & Dermatologic Surgery 21, no. 2 (2017): 66–71. [Google Scholar]
  • 26. Alshehri M. D., Almutairi A. T., Alomran A. M., Alrashed B. A., and Kaliyadan F., “Over‐The‐Counter and Prescription Medications for Acne: A Cross‐Sectional Survey in a Sample of University Students in Saudi Arabia,” Indian Dermatology Online Journal 8, no. 2 (2017): 120–123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Mullaaziz D., Akkaya V. B., and Erturan İ., “Evaluation of the Use of Complementary and Alternative Therapy in Patients With Psoriasis and Acne Vulgaris,” Turkish Archives of Dermatology and Venereology 53, no. 2 (2019): 60–64. [Google Scholar]
  • 28. Duru P. and Orsal O., “The Effect of Acne on Quality of Life, Social Appearance Anxiety, and Use of Conventional, Complementary, and Alternative Treatments,” Complementary Therapies in Medicine 56 (2021): 102614. [DOI] [PubMed] [Google Scholar]
  • 29. Alrabiah Z., Arafah A., Rehman M. U., et al., “Prevalence and Self‐Medication for Acne Among Students of Health‐Related Science Colleges at King Saud University in Riyadh Region Saudi Arabia,” Medicina 59, no. 1 (2022): 52. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Kayiran M. A., Karadag A. S., Alyamac G., et al., “Use of Complementary and Alternative Medicine Among Patients With Acne Vulgaris and Factors Perceived to Trigger the Disease: A Multicentre Cross‐Sectional Study With 1571 Patients,” Indian Journal of Dermatology 67, no. 3 (2022): 311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Yahya H., “Acne Vulgaris in Nigerian Adolescents—Prevalence, Severity, Beliefs, Perceptions, and Practices,” International Journal of Dermatology 48, no. 5 (2009): 498–505. [DOI] [PubMed] [Google Scholar]
  • 32. Ali‐Shtayeh M. S., Jamous R. M., Jamous R. M., and Salameh N. M., “Complementary and Alternative Medicine (CAM) Use Among Hypertensive Patients in Palestine,” Complementary Therapies in Clinical Practice 19, no. 4 (2013): 256–263. [DOI] [PubMed] [Google Scholar]
  • 33. Zyoud S. H., Al‐Jabi S. W., Sweileh W. M., et al., “Use of Complementary and Alternative Medicines in Haemodialysis Patients: A Cross‐Sectional Study From Palestine,” BMC Complementary and Alternative Medicine 16, no. 1 (2016): 204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Quzmar Y., Istiatieh Z., Nabulsi H., Zyoud S. H., and Al‐Jabi S. W., “The Use of Complementary and Alternative Medicine During Pregnancy: A Cross‐Sectional Study From Palestine,” BMC Complementary Medicine and Therapies 21, no. 1 (2021): 108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Al‐Jabi S. W., Khader M., Hamarsha I., et al., “Complementary and Alternative Medicine Use Among Pediatrics in Palestine: A Cross‐Sectional Study,” BMC Pediatrics 21, no. 1 (2021): 503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Awawdeh S., Dabash D., and Salahat H., “Prevalence of Acne and Its Impact on the Quality of Life and Practices Regarding Self‐Treatment Among Medical Students in Palestine,” Scientific Reports 14, no. 1 (2021): 10.1038/s41598-024-55094-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Obesity WHOCo , World Health O: Obesity: Preventing and Managing the Global Epidemic: Report of a WHO Consultation (Switzerland: World Health Organization, 2000). [PubMed] [Google Scholar]
  • 38. Weir C. B. and Jan A., “BMI Classification Percentile and Cut off Points,” in StatPearls. editor by Weir C. B., and Jan A., vol. 76 (Treasure Island, FL: StatPearls Publishing, 2024), 300–315. [PubMed] [Google Scholar]
  • 39. Millstine D., “Types of Complementary and Alternative Medicine—Special Subjects,” in The Merck Manuals, eds. Falk S.. (Rahway, NJ, USA: Merck & Co, 2022). [Google Scholar]
  • 40. Rehman A., Ul‐Ain Baloch N., and Awais M., “Practice of Cupping (Hijama) and the Risk of Bloodborne Infections,” American Journal of Infection Control 42, no. 10 (2014): 1139. [DOI] [PubMed] [Google Scholar]
  • 41. Substance A., Mental Health Services A: National Survey on Drug Use and Health, 2008: Codebook (Rockville: SAMHSA, Office of Applied Studies, 2009). [Google Scholar]
  • 42. Al Robaee A. A., “Prevalence, Knowledge, Beliefs and Psychosocial Impact of Acne in University Students in Central Saudi Arabia,” Saudi Medical Journal 26, no. 12 (2005): 1958–1961. [PubMed] [Google Scholar]
  • 43. Wei B., Pang Y., Zhu H., et al., “The Epidemiology of Adolescent Acne in North East China,” Journal of the European Academy of Dermatology and Venereology 24, no. 8 (2010): 953–957. [DOI] [PubMed] [Google Scholar]
  • 44. Wolkenstein P., Misery L., Amici J. M., et al., “Smoking and Dietary Factors Associated With Moderate‐To‐Severe Acne in French Adolescents and Young Adults: Results of a Survey Using a Representative Sample,” Dermatology 230, no. 1 (2015): 34–39. [DOI] [PubMed] [Google Scholar]
  • 45. Bagatin E., Timpano D. L., Guadanhim L. R., et al., “Acne Vulgaris: Prevalence and Clinical Forms in Adolescents From Sao Paulo, Brazil,” Anais Brasileiros de Dermatologia 89, no. 3 (2014): 428–435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Bhate K. and Williams H. C., “Epidemiology of Acne Vulgaris,” British Journal of Dermatology 168, no. 3 (2013): 474–485. [DOI] [PubMed] [Google Scholar]
  • 47. Aksu A. E., Metintas S., Saracoglu Z. N., et al., “Acne: Prevalence and Relationship With Dietary Habits in Eskisehir, Turkey,” Journal of the European Academy of Dermatology and Venereology 26, no. 12 (2012): 1503–1509. [DOI] [PubMed] [Google Scholar]
  • 48. Lynn D. D., Umari T., Dunnick C. A., and Dellavalle R. P., “The Epidemiology of Acne Vulgaris in Late Adolescence,” Adolescent Health, Medicine and Therapeutics 7 (2016): 13–25. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49. Khafagi I., Zakaria A., Dewedar A., and El‐Zahdany K., “A Voyage in the World of Plants as Mentioned in the Holy Quran,” International Journal of Botany 2, no. 3 (2006): 242–251. [Google Scholar]
  • 50. Kahrizi D., Molsaghi M., Faramarzi A., et al., “Medicinal Plants in Holy Quran,” American Journal of Scientific Research 42 (2012): 62–71. [Google Scholar]
  • 51. Ali‐Shtayeh M. S., Jamous R. M., Salameh N. M., Jamous R. M., and Hamadeh A. M., “Complementary and Alternative Medicine Use Among Cancer Patients in Palestine With Special Reference to Safety‐Related Concerns,” Journal of Ethnopharmacology 187 (2016): 104–122. [DOI] [PubMed] [Google Scholar]
  • 52. Samara A. M., Barabra E. R., Quzaih H. N., and Zyoud S. H., “Use and Acceptance of Complementary and Alternative Medicine Among Medical Students: A Cross Sectional Study From Palestine,” BMC Complementary and Alternative Medicine 19, no. 1 (2019): 78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53. Moon S.‐H., Kwon T.‐G., and Lee S.‐K., “Use of Complementary and Alternative Medicine for Treatment of Acne in Patients in Busan: Results of a Survey,” Korean Journal of Dermatology 2017 (2017): 401–409. [Google Scholar]
  • 54. Orafidiya L., “The Effect of Aloe Vera Gel on the Anti‐Acne Properties of the Essential Oil of Ocimum gratissimum Linn Leaf—A Preliminary Clinical Investigation,” International Journal of Aromatherapy 14, no. 1 (2004): 15–21. [Google Scholar]
  • 55. Zhong H., Li X., Zhang W., Shen X., Lu Y., and Li H., “Efficacy of a New Non‐Drug Acne Therapy: Aloe Vera Gel Combined With Ultrasound and Soft Mask for the Treatment of Mild to Severe Facial Acne,” Frontiers in Medicine 8 (2021): 662640. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56. Al‐Atif H. M., Al‐Ghamdi H. S., Alzubaidi W. A., Alnaem N. M., and Qahtani S. H., “The Prevalence of Complementary and Alternative Medications Use Among Dermatology Patients in Aseer Region, Saudi Arabia,” Clinical, Cosmetic and Investigational Dermatology 15 (2022): 2607–2615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57. “Palestinian Central Bureau of Statistics—Department of User S: An Email: Health Statistics of Dermatologists,” 2023.
  • 58. Jia X., Pang Y., and Liu L. S., “Online Health Information Seeking Behavior: A Systematic Review,” Health 9, no. 12 (2021): 1740. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59. Milan F. B., Landau C., Murphy D. R., et al., “Teaching Residents About Complementary and Alternative Medicine in the United States,” Journal of General Internal Medicine 13, no. 8 (1998): 562–567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60. Kemper K. J., Vincent E. C., and Scardapane J. N., “Teaching an Integrated Approach to Complementary, Alternative, and Mainstream Therapies for Children: A Curriculum Evaluation,” Journal of Alternative and Complementary Medicine 5, no. 3 (1999): 261–268. [DOI] [PubMed] [Google Scholar]
  • 61. Lebensohn P., Kligler B., Dodds S., et al., “Integrative Medicine in Residency Education: Developing Competency Through Online Curriculum Training,” Journal of Graduate Medical Education 4, no. 1 (2012): 76–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62. Gardiner P., Filippelli A. C., Lebensohn P., and Bonakdar R., “Family Medicine Residency Program Directors Attitudes and Knowledge of Family Medicine CAM Competencies,” Explorer 9, no. 5 (2013): 299–307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63. Ertel K., Dooley C., Focht H., and Moak J., “Gender Differences in Attitudes and Practices Toward Body Skin Care,” Journal of the American Academy of Dermatology 60 (2009): AB85. [Google Scholar]
  • 64. Kristoffersen A. E., Stub T., Salamonsen A., Musial F., and Hamberg K., “Gender Differences in Prevalence and Associations for Use of CAM in a Large Population Study,” BMC Complementary and Alternative Medicine 14, no. 1 (2014): 463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65. Alwhaibi M. and Sambamoorthi U., “Sex Differences in the Use of Complementary and Alternative Medicine Among Adults With Multiple Chronic Conditions,” Evidence‐Based Complementary and Alternative Medicine 2016 (2016): 2067095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66. Rhee T. G. and Harris I. M., “Gender Differences in the Use of Complementary and Alternative Medicine and Their Association With Moderate Mental Distress in U.S. Adults With Migraines/Severe Headaches,” Headache 57, no. 1 (2017): 97–108. [DOI] [PubMed] [Google Scholar]
  • 67. Suh D. H., Shin J. W., Min S. U., et al., “Treatment‐Seeking Behaviors and Related Epidemiological Features in Korean Acne Patients,” Journal of Korean Medical Science 23, no. 6 (2008): 969–974. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data collected and analyzed for this study are available from the corresponding author upon reasonable request.


Articles from Journal of Cosmetic Dermatology are provided here courtesy of Wiley

RESOURCES