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Completed

NCT Number: NCT04949789

Pilot Study to Evaluate Efficacy of Botanical Extracts as Protein Amplifier for Skeletal Muscle Strength & Growth.

Sponsor proposes ingredients that when added to daily whey supplementation, can lead to increased muscle strength, improves sleep quality and reduction in fatigue level.

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Key information

Conditions

Age range

20 year–35 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Vedic Lifesciences

Mumbai, Maharashtra, 411046, India

About this study

The present study is a randomized, blinded, placebo-controlled, pilot study. Approximately 40 males aged between ≥ 20 and ≤ 35 years, will be screened. Each trial arm will have at least 5 completed after accounting for dropout/withdrawal rate of 20%. The treatment duration for all the study participants will be 28 to 56 days (Day 56 is only applicable for participants with less than 10% increase in weight leg pressed for 1 RM on Day 28. All participants in arm 1 of study will have their end of study visit on Day 28).Sponsor proposes ingredients that when added to daily whey supplementation, can lead to increased muscle strength, improves sleep quality and reduction in fatigue level.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males aged 20 - 35 years with active lifestyle moderate physical activity level as per International Physical Activity Questionnaire.
  • Recreationally active but not participating in resistance type training on regular basis.
  • Body mass index (BMI) 22 - 29.9 kg/ m2
  • Participants with an Insomnia Severity Index score ≥7 and ≤14
  • Ready to refrain from caffeinated products and intense strength/ endurance exercise for 24 hrs. prior to the exercise lab visit.
  • Fasting Glucose ≤ 110 mg/ dl
  • Systolic Blood Pressure ≤ 129 mm Hg and Diastolic Blood Pressure ≤ 89 mm Hg
  • TSH (thyroid stimulating hormone) ≥0.4 and ≤ 4.9 mIU/L

Exclusion criteria

  • Engaged in structured weight training during the previous 12 months prior to screening.
  • Presence of chronic disease.
  • Changes in body weight more than 4.5 kg (10 pounds) in the past three months.
  • Participants with uncontrolled hypertension.
  • Participants who are diagnosed with Type II Diabetes Mellitus.
  • History or presence of clinically significant renal, hepatic, endocrine, biliary, gastrointestinal, pancreatic, or neurologic disorders.
  • Allergy to whey or herbal ingredients.
  • Participants who have any other disease or condition, or are using any medication, that in the judgment of the investigator would put them at unacceptable risk for participation in the study or may interfere with evaluations in the study or noncompliance with treatment or visits.
  • Participants who have been part of a clinical trial within 90 days prior to the screening.
  • Participants who have used whey or other supplemental proteins anytime in last 3 months

Treatment and study plan

Placebo without Exercise

Other

2 Capsules to be taken 30 minutes before breakfast.

Placebo with Exercise

Other

2 Capsules to be taken 30 minutes before breakfast.

IP I

Other

2 Capsules to be taken 30 minutes before breakfast.

IP II

Other

2 Capsules to be taken 30 minutes before breakfast.

IP III

Other

2 Capsules to be taken 30 minutes before breakfast.

Primary outcomes

  1. 1-Repetition Maximum

    Time frame: Day 0 to Day 28 and /or day56

    The final weight lifted successfully for atleast 1 repetition but could not complete 3 repetition will be recorded as 1- RM.

    Change in muscle strength as indicated by increase in 1Repetition Maximum leg press weight

Secondary outcomes

  1. Body fat composition: Lean Muscle Mass by Dual-energy X-ray absorptiometry

    Time frame: Day 0 to Day 28 and /or day56

    Increase in lean muscle mass by DXA

  2. Quality of Sleep: Modified Insomnia Severity Index

    Time frame: Day 0 to Day 28 and /or day56

    Improvement in sleep quality as assessed by the modified Insomnia Severity Index

  3. Visual Analogue Scale for Fatigue

    Time frame: Day 0 to Day 28 and /or day56

    Reduction in fatigue level as assessed by the 11-point Visual Analogue scale for Fatigue

  4. Mid-thigh Girth

    Time frame: Day 0 to Day 28 and /or day56

    Increase in mid-thigh muscle-girth (prior to exercise) at midpoint between inguinal fold and superior border of patella.

  5. Digestive diary

    Time frame: Day 0 to Day 28 and /or day56

    Participants will be asked to fill out a paper/online digestive diary to monitor any significant changes that might occur to the digestive system due to the consumption of WPI and the IP.

    there should be No significant effect on digestive system as per participant digestive diary.

Sponsors and collaborators

Lead sponsor

Vedic Lifesciences Pvt. Ltd.

Industry

Registry information

Official study title

A Randomized, Placebo-controlled, Blinded, Pilot Study to Evaluate Efficacy of Botanical Extracts as Protein Amplifier for Skeletal Muscle Strength & Growth.

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jul 2, 2021
Registry last updated
Feb 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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