Version Changes
Revised. Amendments from Version 1
Kindly note the following changes: Title: Change from ‘preforming’ to ‘performing’ has been done. Abstract: Background (ashwagandha dose corrected as 600mg); Conclusion (removed the term ‘recovery’ as there were no measures for it. Introduction: Sentence referring to citation number 6 has been reframed as “Serum creatine kinase is raised in individuals who regularly participate in endurance exercise, with peak levels seen 48 hours after the exercise.” Sentence referring to citation number 18 is reframed as “A previously published study evaluating muscle strength focused only on male participants.” and rationale behind including both sexes in our study has been added. Methods: Due to repetition, details of ethical approval are removed. (Study design section). A statement regarding the personal history and habits of both study groups has been added. (Subjects section) Number of participants in each group who consumed the capsules with milk has been added. (Interventions section) Under “Outcomes” names of tests done for safety assessment are added. Results: In all the 4 tables, decimal point of one place has been maintained for mean and standard deviation. Figures 3 and 4 have been removed to avoid duplication of data. A statement for the outcomes of clinical tests done for safety and tolerability of Ashwagandha has been added in the “Adverse events and safety parameters” section. Data regarding the same has been made available on figshare repository as extended data. Discussion: A statement regarding milk consumption is added as a limitation. Failure to anticipate lost to follow up in the sample size calculation and study planning has been added. Data availability: Updated URL of figshare repository having the extended data is added. “Extended data” has data related to the results of clinical tests done for safety evaluation. Throughout the article ‘muscle mass’ is replaced with ‘muscle size’; ‘chest press’ with ‘bench press’.
Abstract
Background
Ashwagandha is a well-known Ayurvedic herb used for youthful vigor and wellbeing. This study investigated the effects of 600 mg standardized root extract (>5% withanolides) of Ashwagandha ( Withania somnifera) on muscle size, strength and cardiorespiratory endurance following resistance training.
Methods
In this eight-week, parallel-group, multicenter, randomized, double-blind, placebo-controlled clinical study, 80 healthy male and female participants aged 18-45 years, who engaged in regular physical activity were randomly allocated in a 1:1 ratio to receive Ashwagandha (AG, n=40) 300 mg capsules twice daily for eight weeks, or identical placebo (PB, n=40). Seven (3 AG, 4 PB) participants were excluded due to poor compliance. All participants conducted eight-week resistance training. Study outcomes included muscle strength (1RM bench press and leg extension), muscle size (circumference of arm, chest and upper thigh) and cardio-respiratory endurance (VO 2max) assessed at baseline and at eight weeks. Analysis of covariance (ANCOVA) was used to estimate adjusted differences based on sex, BMI and chest circumference at baseline.
Results
AG caused greater improvement in bench press (males: p = 0.0084; females: p = 0.0005), leg press (males: p = 0.0049; females: p = 0.018) and endurance (males: p <0.0001; females: p <0.0001) as compared to PB. Also, greater improvements in muscle girth for arm, chest and thigh were seen in both male and female participants with AG. No adverse events were reported in the study.
Conclusions
Eight weeks of AG root extract supplementation along with resistance training is effective in improving muscle strength, growth and endurance in both male and female participants. AG root extract could be a safer, effective and low-cost alternative for athletes to improve muscle endurance.
Keywords: Muscle strength, Cardiorespiratory endurance, Muscle girth, Resistance training
Introduction
Resistance training is a specific conditioning technique in which an individual works against a broad spectrum of resistive loads to enhance general health, fitness and performance. 1 A resistance training program comprises a set of well-organized exercises and aids in rhythmic muscular contraction and relaxation against external resistance. The repetition of actions allows the human body to adapt to such resistance and induces strength and endurance over time. 2 – 4 In addition to strength development, resistance training improves immunity, bone and muscle health and overall function of all organs. 5 Furthermore, regular exercise alters biochemical and physiological processes. Serum creatine kinase is raised in individuals who regularly participate in endurance exercise, with peak levels seen 48 hours after the exercise. 6
A major component of physical fitness and resistance training is cardiorespiratory endurance. Maximal oxygen consumption (VO 2max) refers to the maximum amount of oxygen that an individual can utilize during an intense exercise session and is considered a valid measure to estimate cardiovascular fitness. 7 Studies suggest that resistance training enhances VO 2max by improving heart-muscle function, increased blood volume and increased oxygen-carrying capacity. 8
Alongside resistance training and exercises, diet plays a key role in attaining physical and mental fitness and improving overall health. Traditionally, herbs and their extracts have been considered important dietary supplements with multiple health benefits. 9 Several studies have shown multifaceted efficacy of herbs as they can diminish recovery time, improve performance, enhance muscle size and reduce fat levels. 10 , 11 This has resulted in a growing demand for safe and effective herbal supplements to improve endurance and strength performance among athletes and those with an active lifestyle. 12 Withania somnifera, popularly known as Ashwagandha (AG), is a plant that belongs to the Solanaceae family and grows in arid or semi-arid regions. AG is one of the most frequently used medicinal plants in the Ayurvedic system of complementary medicine for a varied range of ailments. It has been used to treat musculoskeletal conditions and improve general vitality and quality of life. 13 – 15 Pharmacologically, AG has been explored extensively for its potential as a versatile health supplement. 13
Sandhu et al. (2010) studied the impact of 500 mg of AG supplementation for eight weeks on aerobic exercise performance and the activity of associated muscles in healthy young adults. There was a significant increase in VO 2max and muscular power. 16 In another study, Raut et al. (2012) explored the safety, tolerability and activity of 750 mg to 1250 mg of AG in healthy volunteers for 30 days and found that AG supplementation increased muscle strength, improved sleep quality and reduced lipid concentrations. 17 Wankhede et al. (2012) also demonstrated that as in adjunction to a resistance training program, 600 mg of AG supplementation for eight weeks increased muscle strength in untrained male adults. 18 Looking at these previous studies, the current study was based on a hypothesis that AG will lead to a significant improvement in muscle strength, muscle growth and cardio-respiratory endurance in the study participants.
Although preliminary studies mentioned above have been conducted, robust human clinical trials evaluating the performance-enhancing effects of standardized AG root extract are still limited. A previously published study evaluating muscle strength focused only on male participants. 18 However, data on muscle strength and endurance in female participants is scarce. Since gender is an important factor affecting serum hormone levels (and subsequent response to effects of exercise) due to physiological factors, this study focussed on testing the responses in both the genders who are regularly active exercising. There is scarcity of data in previously published literature. Therefore, this randomized, double-blind, placebo-controlled study aims to examine the effects of a standardized AG root extract (as a complement to a resistance training program) on changes in muscle strength, muscle growth and cardio-respiratory endurance in active, healthy participants of either sex.
Methods
Ethical approval
The study was approved by the Institutional Ethics Committees of both King George Medical University (Reference number. #202/IEC/R.Cell-18) and M. V. Hospital and Research (Reference number #IEC/01/28/18) and it was prospectively registered with the Clinical Trials Registry of India (Registration# CTRI/2018/07/014969).
Study design
This was a parallel-group=eight-week, multicenter, randomized, double-blind, PB-controlled study. It was conducted in compliance with the Declaration of Helsinki guidelines, the New Drugs and Clinical trials rules 2019 and the Indian Council of Medical Research (ICMR) ethical guidelines for biomedical research on human subjects.
Recruitment and randomization
The recruitment of participants was performed by circulating printed fliers in the purlieu of a gymnasium which served as the site for the training program. This brochure was approved by both institutional ethics committees. Recruitment of participants started on 11 September, 2018 (first visit of first participant) and ended on 28 March, 2019 (last visit of last participant). Subjects were randomly and equally allocated to two groups in 1:1 ratio using stratified randomization (male and female) to receive either an AG capsule standardized root extract (n=40), or PB which looked identical to AG capsule (n=40). The randomization was computer-generated through randomly permuted blocks of 20. Within each block, the number of participants assigned to each of the two treatment arms was equal. The AG and PB capsules were manufactured and packed in identical containers and labeled equivalently, along with unique serial numbers to ensure blinding. The study centers received numbered and sealed envelopes that contained no information about treatment allocation.
Subjects
All participants read and signed an informed consent form before final selection and enrollment in this study. Healthy adults of either sex aged between 18 to 45 years engaging in regular physical activity (gymnasium/strength training exercise at least three months before screening for this study) were considered eligible. Sex of the participants was defined based on self-reporting. Personal history and habits were found similar in both AG and PB groups. Participants agreed to engage in the same exercise schedule and diet regime for the study period as prescribed in the study protocol and if of child-bearing age, agreed to use barrier birth control measures. Participants were excluded if they were taking any nutritional supplements, medications, or steroids used to enhance physical performance. Those with a history of drug abuse, who smoked more than 10 cigarettes a day, or were habitually consuming more than 14 grams of alcohol per day were also excluded. Other exclusion criteria were: any planned participation in any sporting event during the study period; a weight loss of >5 kg in the previous three months; a history of any orthopedic injury or surgery in the past six months; any known hypersensitivity to AG; participation in any clinical study in the past three months; a history of heart disease, diabetes, depression, stroke or neurological disorder. Participants were also excluded if they were taking anti-hypertensive drugs, beta-blockers, beta-agonists, hormonal contraceptives, corticosteroids, or psychotropic substances over the previous three months.
Interventions
Capsules containing either 300 mg of AG standardized root extract (KSM-66, Ixoreal Biomed, CA, US) or 300 mg starch (Shri Kartikeya Pharma, Hyderabad, India) were used for AG and PB groups respectively. Both the AG and PB formulations were cellulose-based hard capsules and identical in appearance, weight, texture and color. Participants were required to take one capsule twice daily with milk or water. Two males and one female consumed capsules with milk in AG group, whereas 3 males and one female in PB group consumed capsules with milk.
The AG root extract is a light yellowish powder extracted using a proprietary process. The green extraction process is devoid of any alcohol or similar solvents, hence maintaining the standards as recommended by traditional Ayurveda. The product, KSM-66 Ashwagandha, contains a high concentration of root extract of this herb and more than 5% of total withanolides as standardized by high-performance liquid chromatography. The batch number of product used was KSM/VG/18/1020. The chemical profile of the study product was confirmed by Shri Kartikeya Pharma, Hyderabad, India.
Sample size
The target sample size was estimated using G*Power (Version 3.1.9.3). It was based on a previously published randomized controlled clinical study evaluating the effect of an AG root extract on muscle strength and recovery. 18 A recently published systematic review on AG also supported this kind of improvement (effect size of 0.67) in physical performance. 19 Considering the previous study, we hypothesized that AG treatment is better than PB by an effect size of 0.6 with regards to change in the one-repetition maximum (1 RM) bench press exercise after eight weeks. To detect an effect size of 0.6 in a two-parallel-group design (1:1) using independent Student t-test, with a 5% risk of type 1 error (alpha) and 80% power, 40 subjects per group were required while considering a 10% drop-out rate. Thus, 80 healthy male and female subjects were recruited in the study.
Resistance training exercise program
The resistance training regimen used in this study was focused on improving muscle strength, increasing muscle size and enhancing cardiorespiratory endurance. Various resistance exercises were chosen with the objective of training targeted muscle groups. Such training programs target the upper and lower body and consist of a series of exercises with suitable resistance, grouped into multiple sets and repetitions as per the National Strength and Conditioning Association’s (NSCA) regulations and guidelines. 20 Each participant was required to complete the training session every alternate day with a one-day complete rest per week. Therefore, participants were training three days per week. Each training session started with a warm-up of low intensity aerobic exercise. Participants were instructed to perform the maximum repetitions possible for each set until exhaustion. The exercise program is detailed in Figure 1, comprising exercises for week 1, week 2 and remainder of the study (weeks 3 to 8).
Figure 1. Exercise protocol.
Data for this study is available in the online repository ‘Figshare’ under the dataset named ‘Ashwagandha_Muscle study’ ( Underlying data). 34
Study outcomes
Primary outcome measures
Muscle strength
Changes in upper and lower body muscular strength were the primary efficacy assessment of this study. As per common practice in sports medicine, muscle strength was assessed by one-repetition maximum (1RM) for bench press and leg press. 1RM testing was performed using NSCA’s protocol. 20 1 RM refers to the maximal load lifted by a participant for one cycle of the exercise. Muscle strength measurements were conducted at baseline (first day of training) and end of the study (after the completion of eight weeks of training and supplementation). The equipment used was a Bench Press (SL7028) manufactured by Impulse and a Leg extension (GCEC340) manufactured by Body Solid Inc.
Secondary outcome measures
Muscle girth
Muscle size was measured at three sites - arm (flexed mid-upper arm), chest (sternum at mid-tidal volume) and upper thigh (just inferior to gluteal fold) of each participant. Measurements were undertaken on the first day of training (baseline) and at end of the study (day 56). Maximal cross-sectional area (CSA) was measured for thigh and arm using the Moritani-DeVries method, 21 whereas, for chest measurement, girth was measured at the level of middle of the sternum by passing a measuring tape under both arms at the end of normal expiration.
Cardiorespiratory endurance (maximum rate of oxygen consumption)
Resistance training and endurance are highly correlated. 22 , 23 Cardiorespiratory endurance measures overall body performance during high-intensity exercises. Studies indicate that resistance training induces an increase in the maximal rate of oxygen consumption (VO 2max). 22 , 23 VO 2max is measured during incremental exercise, most typically on a motorized treadmill. Bruce protocol was used to assess the treadmill test outcomes of all participants. Test score was considered as time taken for the test in minutes and it was converted to estimate a VO 2max score as per the Bruce protocol. 22
Safety assessment and adverse events
Clinical safety was assessed based on the frequency of adverse events reported by the participants. In addition to this subjective report, standard biochemistry tests (hematology, renal function, liver function and thyroid function tests) were also performed along with measurement of vital signs.
Statistical analysis
Data was entered in Microsoft Excel spreadsheet using manual double-entry method to ensure data accuracy. Statistical analyses were done using MedCalc (version 20.011). Efficacy analysis was done on the modified intention to treat (ITT) dataset (n=73), and safety analysis was done on the whole dataset (n=80). Data for continuous variables are presented as means with standard deviation (SD), whereas categorical and discrete data are presented as counts with percentages. Unpaired t-test was used to assess between-group differences. Change in values form baseline to eight weeks were computed from and compared between the two groups using unpaired t-test. Effects of sex, BMI and chest circumference on different parameters were analyzed using analysis of covariance (ANCOVA). Adjusted means with 95% confidence intervals (CI) and effect size (Cohen’s d) were presented for change from baseline. Criteria for effect sizes were based on the standard criteria (<0.2, trivial; 0.2–0.6, small; 0.6–1.2, moderate; 1.2–2.0, large; 2.0–4.0, very large; and >4.0, nearly perfect). 24
Normality assumptions were checked on all variables using a one-sample Shapiro-Wilk test. A p-value lower than 0.05 was considered the threshold to claim statistical significance.
Results
Participant demographics
A total of 92 people were screened for participation in the study, of which 80 met the inclusion criteria and were enrolled in the study ( Figure 2). All enrolled participants completed the eight-week follow-up. However, four subjects (3 males and 1 female) in the PB and three subjects (3 males) in the AG group did not consume supplementation after their second visit. These participants were documented as having poor compliance to treatment and were excluded from the efficacy analysis. Reasons for premature medication discontinuation were reported as unintentional forgetfulness due to travel and other personal issues by these seven subjects. Baseline demographic characteristics and vital signs are detailed in Table 1 and indicate that the study population was homogenous with no significant differences between the treatment and control groups. Baseline parameters across both the groups are displayed in Table 2.
Figure 2. CONSORT flow chart.
Table 1. Baseline demography and vital parameters in two groups.
AG (n=37) | PB (n=36) | Unpaired t-test | ||
---|---|---|---|---|
M=17/F=20 | M=17/F=19 | |||
Mean (SD) | Mean (SD) | p | ||
Age (yrs.) | Male | 25.2 (4.4) | 23.3 (3.9) | 0.165 |
Female | 25.2 (4.5) | 23.9 (4.8) | 0.528 | |
Total | 25.2 (4.4) | 23.7 (4.3) | 0.155 | |
Pulse (per min) | Male | 78.4 (3.4) | 77.6 (5.1) | 0.484 |
Female | 79.0 (4.5) | 76.9 (2.1) | 0.264 | |
Total | 78.8 (4.0) | 77.3 (3.8) | 0.213 | |
Systolic BP (mm Hg) | Male | 126.8 (5.9) | 124.6 (4.5) | 0.589 |
Female | 126.0 (5.2) | 127.1 (5.5) | 0.476 | |
Total | 126.3 (5.5) | 125.9 (5.2) | 0.321 | |
Diastolic BP (mm Hg) | Male | 79.2 (3.5) | 78.2 (4.3) | 0.936 |
Female | 78.3 (4.6) | 79.6 (4.4) | 0.439 | |
Total | 78.7 (4.1) | 78.9 (4.3) | 0.165 |
AG: Ashwagandha; PB: Placebo.
Table 2. Baseline parameters in two groups.
AG (n=37) | PB (n=36) | Unpaired t-test | ||
---|---|---|---|---|
M=17/F=20 | M=17/F=19 | |||
Mean (SD) | Mean (SD) | p | ||
Weight (kg) | Male | 62.1 (6.7) | 60.3 (4.7) | 0.351 |
Female | 54.9 (4.0) | 54.3 (4.3) | 0.706 | |
Total | 58.2 (6.4) | 57.1 (5.4) | 0.451 | |
BMI (kg/sq.m) | Male | 23.5 (1.0) | 22.5 (1.9) | 0.059 |
Female | 23.0 (0.9) | 22.7 (1.4) | 0.382 | |
Total | 23.2 (1.0) | 22.6 (1.6) | 0.049 | |
Body fat (%) | Male | 23.8 (2.7) | 25.0 (2.3) | 0.157 |
Female | 29.0 (5.0) | 28.3 (3.4) | 0.771 | |
Total | 26.6 (4.8) | 26.7 (3.3) | 0.718 | |
1-RM Bench Press (kg) | Male | 51.8 (7.8) | 54.8 (7.5) | 0.261 |
Female | 49.0 (5.0) | 51.4 (6.4) | 0.221 | |
Total | 50.3 (6.5) | 53.0 (7.0) | 0.270 | |
1-RM Leg Press (kg) | Male | 60.1 (6.4) | 59.5 (9.5) | 0.848 |
Female | 60.0 (6.7) | 59.7 (8.4) | 0.907 | |
Total | 60.0 (6.4) | 59.6 (8.8) | 0.553 | |
Max. VO 2 (ml/kg/min) | Male | 38.2 (1.4) | 37.8 (2.4) | 0.804 |
Female | 28.8 (1.4) | 28.7 (1.4) | 0.817 | |
Total | 33.1 (5.0) | 33.0 (5.0) | 0.982 | |
Mid-arm circumference (cm) | Male | 31.1 (2.9) | 30.2 (2.1) | 0.185 |
Female | 29.2 (3.0) | 27.3 (3.1) | 0.063 | |
Total | 30.1 (3.1) | 28.6 (3.0) | 0.029 | |
Thigh circumference (cm) | Male | 58.5 (4.2) | 55.8 (10.0) | 0.307 |
Female | 57.8 (6.1) | 57.3 (7.4) | 0.894 | |
Total | 58.1 (5.3) | 56.6 (8.6) | 0.396 | |
Chest circumference (cm) | Male | 92.2 (6.0) | 88.2 (7.5) | 0.019 |
Female | 88.2 (3.5) | 84.8 (4.2) | 0.031 | |
Total | 90.0 (5.2) | 86.4 (6.2) | 0.002 |
AG: Ashwagandha; PB: Placebo.
Muscle strength
Changes in 1 RM bench press and leg press across both treatment groups throughout the eight-week trial period are detailed in Table 3. There were significant differences between the groups in both 1 RM bench press (males: effect size, 0.91; p=0.0084; females: effect size, 1.56; p=0.0005; total: effect size, 1.14; p<0.0001) and 1 RM Leg press (males: effect size, 1.22; p=0.0049; females: effect size, 0.63; p=0.018; total: effect size, 1.11; p=0.0005). A within-group analysis in AG group demonstrated a significant (p<0.0001) increase of 23.5 % and 22.8% in 1 RM bench press and an increase of 15% and 9.9% in 1 RM leg press over time and in both male and female participants respectively. Table 4 presents the comparison of AG and PB for change (unadjusted and adjusted for baseline values) in 1 RM leg press and 1 RM bench press from baseline to eight weeks.
Table 3. Change from baseline at 8 weeks in two groups (Univariate tests).
AG (n=37) | PB (n=36) | Unpaired t-test | ||
---|---|---|---|---|
M=17/F=20 | M=17/F=19 | |||
Mean (SD) | Mean (SD) | ‘p’ | ||
Weight (kg) | Male | 1.4 (1.1) | 1.2 (1.2) | 0.605 |
Female | 1.2 (0.9) | 0.8 (0.8) | 0.114 | |
Total | 1.3 (1.0) | 1.0 (1.0) | 0.177 | |
BMI (kg/sq.m) | Male | 0.5 (0.5) | 0.4 (0.5) | 0.636 |
Female | 0.5 (0.4) | 0.3 (0.3) | 0.079 | |
Total | 0.5 (0.4) | 0.4 (0.4) | 0.140 | |
Body fat (%) | Male | -1.6 (0.3) | -1.7 (0.3) | 0.413 |
Female | -1.7 (0.2) | -1.7 (0.2) | 0.839 | |
Total | -1.7 (0.3) | -1.7 (0.3) | 0.428 | |
1RM Bench Press (kg) | Male | 10.7 (8.5) | 8.8 (7.4) | 0.440 |
Female | 11.2 (6.1) | 9.0 (5.2) | 0.226 | |
Total | 11.0 (7.3) | 8.9 (6.3) | 0.176 | |
1RM Leg Press (kg) | Male | 8.0 (7.4) | 6.2 (5.9) | 0.382 |
Female | 5.9 (10.5) | 2.8 (9.9) | 0.330 | |
Total | 7.0 (9.03) | 4.5 (8.2) | 0.194 | |
Max. VO 2 (ml/kg/min) | Male | 3.6 (1.6) | 1.4 (0.5) | <0.0001 |
Female | 2.0 (0.9) | 1.0 (0.6) | <0.0001 | |
Total | 2.8 (1.5) | 1.2 (0.6) | <0.0001 | |
Mid-arm circumference (cm) | Male | 1.6 (0.4) | 1.2 (0.4) | 0.009 |
Female | 1.5 (0.7) | 1.2 (0.6) | 0.226 | |
Total | 1.5 (0.5) | 1.2 (0.5) | 0.014 | |
Thigh circumference (cm) | Male | 3.4 (3.3) | 2.9 (1.1) | 0.540 |
Female | 0.8 (0.1) | 0.6 (0.2) | 0.009 | |
Total | 2.1 (2.6) | 1.8 (1.4) | 0.519 | |
Chest circumference (cm) | Male | 3.7 (1.7) | 2.9 (1.5) | 0.099 |
Female | 3.5 (2.1) | 2.0 (0.8) | 0.006 | |
Total | 3.6 (1.9) | 2.5 (1.3) | 0.002 |
Within group changes (baseline versus week 8) significant at p<0.05 (paired t-test); AG: Ashwagandha; PB: Placebo.
Table 4. Comparison between AG and PB for change from baseline at 8 weeks in two groups.
Difference (AG – PB) | Effect size | Power | ||||
---|---|---|---|---|---|---|
Unadjusted Mean (95% C.I.) | Adjusted Mean (95% C.I.) | Unadjusted | Adjusted | ‘p’ | ||
Weight (kg) | 0.4 (-0.01 to 0.91) | 0.7 (0.22 to 1.19) | 0.324 | 0.483 | 0.005 | 0.695 |
BMI (kg/sq.m) | 0.2 (0.01 to 0.38) | 0.3 (0.10 to 0.49) | 0.343 | 0.497 | 0.004 | 0.733 |
1RM Bench Press (kg) | 2.1 (-1.08 to 5.20) | 2.5 (-0.96 to 6.04) | 0.218 | 0.241 | 0.152 | 0.214 |
1RM Leg Press (kg) | 2.7 (-1.52 to 6.87) | 4.4 (-0.02 to 8.85) | 0.212 | 0.332 | 0.051 | 0.418 |
Max. VO 2 (ml/kg/min) | 1.5 (0.99 to 2.10) | 1.6 (1.08 to 2.10) | 0.930 | 1.034 | <0.0001 | 1.000 |
Body fat (%) | 0.1 (-0.04 to 0.18) | 0.1 (-0.05 to 0.20) | 0.209 | 0.193 | 0.251 | 0.238 |
Mid-arm circumference (cm) | 0.3 (0.07 to 0.58) | 0.4 (0.16 to 0.70) | 0.420 | 0.526 | 0.002 | 0.865 |
Thigh circumference (cm) | 0.3 (-0.73 to 1.34) | 0.2 (-0.65 to 1.11) | 0.097 | 0.086 | 0.607 | 0.063 |
Chest circumference (cm) | 1.3 (0.49 to 2.06) | 1.3 (0.59 to 2.08) | 0.538 | 0.596 | 0.001 | 0.910 |
Adjusted values based on Analysis of Covariance for change from baseline (Covariates appearing in the model are evaluated at the following values: Sex=1.50, baseline BMI=22.83 kg/sq.m, baseline chest circumference=88.18 cm); AG: Ashwagandha; PB: Placebo.
Muscle size
Changes in muscle size across the two treatment groups during the study period are detailed in Table 3. At the end of the study, there was a significant increase in both chest circumference (Total participants: p=0.019) and arm circumference (Total participants: p<0.0001), among the participants in AG group as compared to the PB group. However, no improvement was seen in thigh circumference when compared to PB group. A within-group analysis in AG group demonstrated a significant increase in the chest circumference (males: p<0.0001; females: p<0.0001), mid-arm circumference (males: p<0.0001; females: p<0.0001) and thigh circumference (males: p=0.0003; females: p<0.0001). Table 4 presents the comparison of AG and PB for change (unadjusted and adjusted for baseline values) for mid-arm, thigh and chest circumference from baseline to eight weeks.
Endurance
Changes in the VO 2max across the two treatment groups throughout the eight-week trial period are detailed in Table 3. At the end of the study, there was a statistically significant between-group difference in VO 2max values (males: p<0.0001; females: p=0.0001), when compared with the PB group. In the AG group=a statistically significant 9.5% and 7% increase were observed over time in both males (p<0.0001) and females (p<0.0001), respectively. Table 4 presents the comparison of AG and PB for change (unadjusted and adjusted for baseline values) in VO 2max from baseline to eight weeks. The analysis for VO 2max yielded 100% power and greater changes were observed with AG as compared to placebo (effect size, 1.034, p<0.0001).
Adverse events and safety parameters
The participants did not report any adverse events during the study period. No significant changes were observed from baseline to week 8 in any of the laboratory tests conducted for hematology, renal function, liver function and thyroid function tests with both AG and PP treated participants (supplementary data). Similarly, no changes in any of the vital parameters was observed at week 8 in both treatment groups. 34
Discussion
The present study assessed the impact of AG root extract supplementation on resistance training adaptations such as muscle strength and endurance in healthy and active adults. The primary findings of the study are that significantly greater improvements in muscle strength for both lower body (1 RM Leg press) and upper body (1 RM Bench press) occurred in participants consuming AG as compared to PB. In addition, AG supplementation significantly increased muscle size and endurance. However, there were no differences in thigh muscle size (male) and body composition (body fat) between the two groups.
The impact of resistance exercise training on increasing muscular strength was better (p<0.05) with AG (23%) versus PB (8%). Similarly, a previous study by Wankhede et al. (2012) reported significant improvements in both bench press and leg extension after eight weeks of the AG supplement in healthy adult males. 18 However, these improvements were greater in comparison to the current study, which could be due to the fact that experiment was conducted on inexperienced individuals in the previous study versus resistance-trained adults in the current investigation. Earlier studies recommended that along with strength and muscle growth, factors such as human growth hormone and testosterone were found higher in males compared to females. 25 Our study also measured the muscular strength of male and female participants (1 RM bench press and leg press), and a significantly greater outcome was found in males than female participants with an exception of 1 RM bench press in females, both before and after the resistance training program. Furthermore, due to resistance training, general development from the baseline parameters was observed for all the participants. This suggests that the improvement was of clinical relevance (effect size, 0.9, indicating larger effect) which is an improvement over the meta-analysis conducted by Bonilla et al. (2021) 19 that analyzed twelve clinical trials of AG on physical performance; however, only two trials were relevant for muscular strength.
The percentage of adults whose chest, thigh and mid-arm muscle size increased differed significantly between the two study groups, although men’s thigh size remained similar in both groups. Furthermore, endurance measured by VO 2max also increased significantly in AG group which suggests that the effect, although small in magnitude (8%), might be clinically relevant. This observation is lower compared to a previous study by Tiwari et al., 26 which reported a 16% improvement in VO 2max. Similarly, another study by Choudhary et al. 27 observed 13% increase in VO 2max after eight weeks of AG supplementation. Therefore, the current improvement is comparable and consistent with literature review.
No significant benefit was seen with respect to body fat, as assessed by the body composition monitor. Slight improvement was seen in AG group, but there was no significant difference between the two groups. However, the study was not powered enough to assess the change in body fat.
AG was well tolerated by the subjects and no serious side effects were reported. This finding is consistent with previously published studies on AG ( Withania somnifera) root extract in healthy volunteers, which also advocated the herb’s tolerance. 17 , 18 , 28 , 29 Thus, it could be a safer alternative to improve and maintain physical performance.
Increased levels of anabolic hormone (serum testosterone) may be the cause of improved muscular strength, which could be associated with its structural similarities to withanolides (major constituents of AG root extract). 30 Most of the studies included in the meta-analysis by Bonilla et al., which involved muscle strength, endurance and recovery might be owed to the antioxidant properties of this plant. 19 In addition, as previously shown, AG alleviates stress, improves sleep and physical performance, 14 , 31 – 33 even though these were not measured in this study.
Our trial had certain strengths, including enrollment of resistance-trained adult men and women, adequate sample size, a double-blind, PB-controlled design, excellent participant retention and use of standardized AG extract. Since it was expected that the study participants were highly motivated adults performing regular exercises, we had not anticipated data loss due to lost to follow-up. However, we had data loss not due to lost to follow-up, but due to poor compliance (3 participants in AG and 4 in PB group). We failed to anticipate this possibility during study planning. However, we estimated the effect size (1.14 and 1.11 for 1-RM bench press and 1-RM leg press respectively) for the primary outcomes, to derive our conclusions. Another noteworthy drawback was the lack of quantitative data on the subjects’ food intake. They were, however, instructed not to change and follow the specified diet for entire length of the trial. Although the subjects claimed to have followed the instructions (as per subject’s diary), we were unable to determine if these factors influenced the effect of AG due to a lack of reliable detailed quantitative information on daily calorie and protein intake. Also, as some participants in both groups consumed the capsules with milk our study lacked to establish the effects of milk consumption on the study parameters. Another limitation is that our research focused on resistance-trained adults for eight weeks, so extrapolating results to other groups for a longer duration should be done with caution. As a result, in future studies, we advocate a comprehensive dietary analysis of participants' daily calorie and protein consumption, as well as a longer-term follow-up with diverse populations.
Conclusions
In conclusion, eight weeks of AG root extract supplementation in combination with resistance training is effective in promoting muscle strength, muscle growth and can also improve endurance in both male and female participants. The study also indicated that the participants have tolerated the AG root extract well. Thus, AG root extract could probably represent a safer low-cost alternative for athletes.
Author contributions
All the authors of this study contributed to the project equally. NV supervised the study at the KGMU hospital and led the study. SKG supervised the study at MV hospital. SP worked on review and editing of the article. ST helped in data collection and analysis. AKM conceptualized the study, helped in data analysis and writing the manuscript. All the authors participated in study designing and implementation and all the authors have gone through the final article and approved it for submission. Every author actively participated in drafting the manuscript and approved the final version of the article.
Acknowledgments
The authors thank Ixoreal BioMed Inc., Los Angeles, California, USA, for supplying the AG high concentration root extract used in this study.
Funding Statement
The author(s) declared that no grants were involved in supporting this work.
[version 2; peer review: 1 approved
Data availability
Underlying data
Figshare: Ashwagandha_Muscle study, https://doi.org/10.6084/m9.figshare.22081895.v4. 34
The project contains the following underlying data:
-
-
Ashwagandha_Muscle study_Raw data.csv
-
-
Ashwagandha_Muscle study_Raw data.xlsx
-
-
Filled consort checklist
-
-
Study protocol
Extended data
Figshare: Ashwagandha_Muscle study, https://doi.org/10.6084/m9.figshare.22081895.v4. 34
This project contains the following extended data:
-
•
Data related to the outcomes of clinical tests done for safety assessment of the participants are available in the Figshare repository.
Reporting guidelines
Figshare: CONSORT checklist for ‘Effects of Ashwagandha ( Withania somnifera) standardized root extract on physical endurance and VO 2max in healthy adults preforming resistance training: An eight-week, prospective, randomized, double-blind, placebo-controlled study’. https://doi.org/10.6084/m9.figshare.22081895.v4. 34
Data are available under the terms of the Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).
References
- 1. Lloyd RS, Faigenbaum AD, Stone MH, et al. : Position statement on youth resistance training: the 2014 International Consensus. Br J Sports Med. 2014 Apr;48(7):498–505. 10.1136/bjsports-2013-092952 [DOI] [PubMed] [Google Scholar]
- 2. Kraemer WJ, Ratamess NA: Fundamentals of Resistance Training: Progression and Exercise Prescription. Med Sci Sport Exerc. 2004 Apr;36(4):674–688. 10.1249/01.MSS.0000121945.36635.61 Reference Source [DOI] [PubMed] [Google Scholar]
- 3. Staron RS, Karapondo DL, Kraemer WJ, et al. : Skeletal muscle adaptations during early phase of heavy-resistance training in men and women. J Appl Physiol. 1994 Mar 1;76(3):1247–1255. 10.1152/jappl.1994.76.3.1247 [DOI] [PubMed] [Google Scholar]
- 4. Sale DG: Neural adaptation to resistance training. Med Sci Sport Exerc. 1988 Oct;20(Sup 1):S135–S145. 10.1249/00005768-198810001-00009 Reference Source [DOI] [PubMed] [Google Scholar]
- 5. Nieman DC, Wentz LM: The compelling link between physical activity and the body’s defense system. J Sport Heal Sci. 2019 May;8(3):201–217. 10.1016/j.jshs.2018.09.009 Reference Source [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Totsuka M, Nakaji S, Suzuki K, et al. : Break point of serum creatine kinase release after endurance exercise. J Appl Physiol. 2002 Oct 1;93(4):1280–1286. 10.1152/japplphysiol.01270.2001 [DOI] [PubMed] [Google Scholar]
- 7. Jones GL, Killian KJ, Summers E, et al. : Inspiratory muscle forces and endurance in maximum resistive loading. J Appl Physiol. 1985 May 1;58(5):1608–1615. 10.1152/jappl.1985.58.5.1608 [DOI] [PubMed] [Google Scholar]
- 8. Hellsten Y, Nyberg M: Cardiovascular Adaptations to Exercise Training. Comprehensive Physiology. Wiley;2015; pp.1–32. 10.1002/cphy.c140080 [DOI] [PubMed] [Google Scholar]
- 9. Probst YC, Guan VX, Kent K: Dietary phytochemical intake from foods and health outcomes: a systematic review protocol and preliminary scoping. BMJ Open. 2017 Feb 15;7(2):e013337. 10.1136/bmjopen-2016-013337 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Konda MR, Alluri KV, Janardhanan PK, et al. : Combined extracts of Garcinia mangostana fruit rind and Cinnamomum tamala leaf supplementation enhances muscle strength and endurance in resistance trained males. J Int Soc Sports Nutr. 2018 Jan 5;15(1):50. 10.1186/s12970-018-0257-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. Chen CK, Muhamad AS, Ooi FK: Herbs in exercise and sports. J Physiol Anthropol. 2012 Dec 8;31(1):4. 10.1186/1880-6805-31-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Williams MH: Dietary Supplements and Sports Performance: Introduction and Vitamins. J Int Soc Sports Nutr. 2004 Dec 1;1(2):1–6. 10.1186/1550-2783-1-2-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Mishra LC, Singh BB, Dagenais S: Scientific basis for the therapeutic use of Withania somnifera (ashwagandha): a review. Altern Med Rev. 2000 Aug;5(4):334–346. [PubMed] [Google Scholar]
- 14. Chandrasekhar K, Kapoor J, Anishetty S: A Prospective, Randomized Double-Blind, Placebo-Controlled Study of Safety and Efficacy of a High-Concentration Full-Spectrum Extract of Ashwagandha Root in Reducing Stress and Anxiety in Adults. Indian J Psychol Med. 2012 Jul 1;34(3):255–262. 10.4103/0253-7176.106022 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Archana R, Namasivayam A: Antistressor effect of Withania somnifera. J Ethnopharmacol. 1998 Jan;64(1):91–93. 10.1016/S0378-8741(98)00107-X Reference Source [DOI] [PubMed] [Google Scholar]
- 16. Sandhu J, Shah B, Shenoy S, et al. : Effects of Withania somnifera (Ashwagandha) and Terminalia arjuna (Arjuna) on physical performance and cardiorespiratory endurance in healthy young adults. Int J Ayurveda Res. 2010;1(3):144–149. 10.4103/0974-7788.72485 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Raut A, Rege N, Shirolkar S, et al. : Exploratory study to evaluate tolerability, safety, and activity of Ashwagandha (Withania somnifera) in healthy volunteers. J Ayurveda Integr Med. 2012;3(3):111–114. 10.4103/0975-9476.100168 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Wankhede S, Langade D, Joshi K, et al. : Examining the effect of Withania somnifera supplementation on muscle strength and recovery: a randomized controlled trial. J Int Soc Sports Nutr. 2015 Oct 20;12(1):43. 10.1186/s12970-015-0104-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Bonilla DA, Moreno Y, Gho C, et al. : Effects of Ashwagandha (Withania somnifera) on Physical Performance: Systematic Review and Bayesian Meta-Analysis. J Funct Morphol Kinesiol. 2021 Feb 11;6(1):20. 10.3390/jfmk6010020 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Haff G, Triplett N: Essentials of strength training and conditioning. 4th ed. United States, Champaign, IL: Human Kinetics;2016; pp.264–470. [Google Scholar]
- 21. DeFreitas JM, Beck TW, Stock MS, et al. : A Comparison of Techniques for Estimating Training-Induced Changes in Muscle Cross-Sectional Area. J Strength Cond Res. 2010 Sep;24(9):2383–2389. 10.1519/JSC.0b013e3181ec86f3 Reference Source [DOI] [PubMed] [Google Scholar]
- 22. Gäbler M, Prieske O, Hortobágyi T, et al. : The Effects of Concurrent Strength and Endurance Training on Physical Fitness and Athletic Performance in Youth: A Systematic Review and Meta-Analysis. Front Physiol. 2018 Aug 7;9. 10.3389/fphys.2018.01057/full [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Hughes DC, Ellefsen S, Baar K: Adaptations to Endurance and Strength Training. Cold Spring Harb Perspect Med. 2018 Jun;8(6):a029769. 10.1101/cshperspect.a029769 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Cohen J: Statistical Power Analysis for the Behavioral Sciences. Elsevier;1977. Reference Source [Google Scholar]
- 25. Kraemer W, Gordon S, Fleck S, et al. : Endogenous Anabolic Hormonal and Growth Factor Responses to Heavy Resistance Exercise in Males and Females. Int J Sports Med. 1991 Apr 14;12(02):228–235. 10.1055/s-2007-1024673 [DOI] [PubMed] [Google Scholar]
- 26. Tiwari S, Gupta SK, Pathak AK: A double-blind, randomized, placebo-controlled trial on the effect of Ashwagandha (Withania somnifera dunal.) root extract in improving cardiorespiratory endurance and recovery in healthy athletic adults. J Ethnopharmacol. 2021 May;272:113929. 10.1016/j.jep.2021.113929 Reference Source [DOI] [PubMed] [Google Scholar]
- 27. Choudhary B, Shetty A, Langade D: Efficacy of Ashwagandha (Withania somnifera [L.] Dunal) in improving cardiorespiratory endurance in healthy athletic adults. AYU (An Int Q J Res Ayurveda). 2015;36(1):63. Reference Source [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Lopresti AL, Drummond PD, Smith SJ: A Randomized, Double-Blind, Placebo-Controlled, Crossover Study Examining the Hormonal and Vitality Effects of Ashwagandha (Withania somnifera) in Aging, Overweight Males. Am J Mens Health. 2019 Mar 10;13(2):155798831983598. 10.1177/1557988319835985 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29. Kuchewar V, Borkar M, Nisargandha M: Evaluation of antioxidant potential of Rasayana drugs in healthy human volunteers. AYU (An Int Q J Res Ayurveda). 2014;35(1):46–49. 10.4103/0974-8520.141919 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Mirjalili M, Moyano E, Bonfill M, et al. : Steroidal Lactones from Withania somnifera, an Ancient Plant for Novel Medicine. Molecules. 2009 Jul 3;14(7):2373–2393. 10.3390/molecules14072373 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Salve J, Pate S, Debnath K, et al. : Adaptogenic and Anxiolytic Effects of Ashwagandha Root Extract in Healthy Adults: A Double-blind, Randomized, Placebo-controlled Clinical Study. Cureus. 2019 Dec 25;11:e6466. 10.7759/cureus.6466 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32. Langade D, Kanchi S, Salve J, et al. : Efficacy and Safety of Ashwagandha (Withania somnifera) Root Extract in Insomnia and Anxiety: A Double-blind, Randomized, Placebo-controlled Study. Cureus. 2019 Sep 28;11:e5797. 10.7759/cureus.5797 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Langade D, Thakare V, Kanchi S, et al. : Clinical evaluation of the pharmacological impact of ashwagandha root extract on sleep in healthy volunteers and insomnia patients: A double-blind, randomized, parallel-group, placebo-controlled study. J Ethnopharmacol. 2021 Jan;264:113276. 10.1016/j.jep.2020.113276 Reference Source [DOI] [PubMed] [Google Scholar]
- 34. Verma N, Gupta SK, Patil S, et al. : Ashwagandha_Muscle study.Dataset. figshare. 2023. 10.6084/m9.figshare.22081895.v4 [DOI]