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Whey Protein and Adaptogenic Supplementation in Physically Active Females

Whey Protein and Adaptogenic Herb Supplementation in Physically Active Females: A Randomised Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07594444
Enrollment
60
Registered
2026-05-18
Start date
2026-07-01
Completion date
2026-09-20
Last updated
2026-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Strength, Muscle Strength Recovery, Recovery, Sports Nutritional Sciences, Supplements

Keywords

Whey Protein, Plant protein, Ashwagandha, Shatavari, Adaptogens, Sports, Exercise, Active females, physically active females

Brief summary

The goal of this clinical trial is to learn whether whey protein or plant protein supplements, with or without an adaptogenic herb blend, can improve strength, recovery, stress, and wellbeing in active females. The adaptogenic blend contains ashwagandha root extract and shatavari root extract. The main questions the study aims to answer are: * Do whey protein and plant protein supplements improve muscle strength and recovery in physically active females? * Does adding ashwagandha and shatavari improve stress, recovery, sleep, and wellbeing compared with protein alone? * Are there differences between whey protein and plant protein when combined with the adaptogenic blend? Researchers will compare four supplement groups: * Whey protein * Whey protein with ashwagandha and shatavari * Plant protein * Plant protein with ashwagandha and shatavari Participants will: * Take their assigned supplement daily for 6 weeks * Attend testing sessions before and after the intervention * Complete questionnaires about recovery, sleep, stress, soreness, and digestive health * Provide saliva samples to measure stress, hormone, immune, and inflammation markers * Complete muscle strength tests, including handgrip strength and push-up testing * Complete a 24-hour dietary recall. The study includes physically active females aged 18 to 45 years who regularly participate in structured training.

Interventions

DIETARY_SUPPLEMENTWhey protein

Participants will consume a whey protein supplement daily for 6 weeks. The supplement will be provided in identical blank tubs. Participants will be instructed to maintain their usual diet and training habits throughout the intervention period.

DIETARY_SUPPLEMENTWhey Protein With Adaptogenic Blend

Participants will consume a whey protein supplement containing ashwagandha KSM-66® root extract (250 mg) and shatavari SRI-81™ root extract (300 mg) daily for 6 weeks. Supplements will be provided in identical blank tubs. Participants will maintain usual diet and training habits during the study.

DIETARY_SUPPLEMENTPlant Protein Supplement

Participants will consume a plant-based protein supplement daily for 6 weeks. The supplement will be provided in identical blank tubs. Participants will be instructed to maintain their usual diet and training habits throughout the intervention period.

DIETARY_SUPPLEMENTPlant Protein With Adaptogenic Blend

Participants will consume a plant-based protein supplement containing ashwagandha KSM-66® root extract (250 mg) and shatavari SRI-81™ root extract (300 mg) daily for 6 weeks. Supplements will be provided in identical blank tubs. Participants will maintain usual diet and training habits during the study.

Sponsors

Sports Performance and Applied Research in Trials and Analysis
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Masking description

Participants and outcome assessors will be blinded to group allocation. Supplements will be provided in identical blank tubs to minimise identification of the assigned intervention. Group allocation codes will be concealed until completion of data collection and primary analyses.

Intervention model description

Participants will be randomly assigned to 1 of 4 parallel groups: whey protein, whey protein with adaptogenic blend, plant protein, or plant protein with adaptogenic blend. Participants will remain in their assigned group for the full 6-week intervention period. Baseline and post-intervention assessments will be conducted to compare changes between groups and over time.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Female, aged 18-45 years * Currently participating in regular structured athletic or physical training (≥3 sessions per week) * Free from musculoskeletal injury that would prevent testing * Willing to maintain usual diet and training habits during the study * Not currently using protein supplements or adaptogenic supplements

Exclusion criteria

* Pregnant, breastfeeding, or planning pregnancy during the study period * Known allergy or sensitivity to dairy, pea protein, pumpkin seed, chia seed, ashwagandha, shatavari, or nightshades * Current use of prescribed medication that may interact with the supplements * Thyroid disorders, autoimmune conditions, hormone-sensitive conditions, or other medical conditions that may be affected by supplementation * Diagnosed eating disorder or condition affecting protein metabolism * Current musculoskeletal injury preventing participation in testing * Current use of other protein supplements or adaptogens

Design outcomes

Primary

MeasureTime frameDescription
Salivary Cortisol ConcentrationBaseline and Week 6Change in salivary cortisol concentration from baseline to post-intervention following 6 weeks of whey protein or plant protein supplementation with or without an adaptogenic herb blend containing ashwagandha KSM-66® and shatavari SRI-81™. Results will be reported in ng/mL.

Secondary

MeasureTime frameDescription
Handgrip StrengthBaseline and Week 6Change in maximal handgrip strength measured using a CAMRY dynamometer from baseline to post-intervention.
Upper Body Muscular EnduranceBaseline and Week 6Change in upper body muscular endurance assessed using the 90-degree push-up test protocol from baseline to post-intervention.
Perceived Recovery and WellbeingBaseline and Week 6Participants will complete the Hooper Index Questionnaire, which assesses four domains: sleep quality, fatigue, stress, and muscle soreness. Each domain is rated on a 10-point Likert scale ranging from 1 to 10, with total scores ranging from 4 to 40. Higher scores indicate poorer wellbeing and recovery status, whereas lower scores indicate better perceived wellbeing and recovery.
Salivary DHEA-S ConcentrationBaseline and Week 6Salivary DHEA-S concentration will be measured from saliva samples using enzyme-linked immunosorbent assay (ELISA) techniques. Results will be reported in ng/mL.
Perceived Gastrointestinal HealthBaseline and Week 6Change in gastrointestinal symptoms and digestive comfort assessed using a gastrointestinal distress questionnaire.
Dietary IntakeBaseline and Week 6Dietary intake assessed using a 24-hour dietary recall to evaluate habitual nutritional intake during the study period.
Salivary Oestradiol ConcentrationBaseline and Week 6Salivary oestradiol concentration will be measured from saliva samples using ELISA. Results will be reported in pg/mL.
Salivary Secretory Immunoglobulin A (sIgA) ConcentrationBaseline and Week 6Salivary secretory immunoglobulin A (sIgA) concentration will be measured from saliva samples using ELISA. Results will be reported in µg/mL.
Salivary C-reactive Protein ConcentrationBaseline to Week 6Salivary C-reactive protein will be measured from saliva samples using ELISA. Results will be reported in pg/mL.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 6, 2026