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COMPLETED NA

Ashwagandha Extract for Weight and Stress Management in Overweight and Obese Adults

NCT07215455 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to evaluate the effects of KSM-66 Ashwagandha root extract (300 mg daily) on weight management and stress reduction in overweight and obese adults. Ashwagandha (Withania somnifera) is a traditional herbal supplement that may help reduce stress and support overall health. In this randomized, double-blind, placebo-controlled trial, participants will receive either Ashwagandha extract or a placebo for the study duration. The main goal is to measure changes in body weight and stress levels. Other health outcomes, such as body mass index (BMI), waist circumference, and quality of life, will also be assessed. The study will help determine whether Ashwagandha is effective and safe for managing stress and supporting weight loss in adults with overweight or obesity.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Ashwagandha 300 mg standardized root extract
  • OTHER Identical placebo capsule.

Study Locations (1)

California

  • San Francisco Research Institute — San Francisco

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-06-17
Est. Completion 2025-10-22
Phase NA

Sponsor

SF Research Institute

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07215455

The ClinicalTrials.gov registry entry for NCT07215455 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SF Research Institute, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Stress appearing as the primary indexed condition, and to 2 interventions — of which Ashwagandha 300 mg standardized root extract is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07215455 reports 1 study location spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07215455 about?

NCT07215455 is a clinical study titled "Ashwagandha Extract for Weight and Stress Management in Overweight and Obese Adults". This study is designed to evaluate the effects of KSM-66 Ashwagandha root extract (300 mg daily) on weight management and stress reduction in overweight and obese adults. Ashwagandha (Withania somnifera) is a traditional herbal supplement that may help reduce stress and support overall health. In th...

What is the current status of trial NCT07215455?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2025-06-17. Estimated completion is 2025-10-22.

What conditions does trial NCT07215455 study?

This clinical trial studies the following conditions: Stress, Weight Management. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07215455?

The interventions under investigation include: Ashwagandha 300 mg standardized root extract (DIETARY_SUPPLEMENT), Identical placebo capsule. (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07215455?

This trial is sponsored by SF Research Institute, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07215455 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial