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NCT04959318
Precision Nutrition Impact on Health-Related Behavior Change
NA trial testing Professional nutrition counseling in Metabolic Syndrome in 138 participants. Completed in 9 July 2021.
9 July 2021
Quick facts
| Lead sponsor | Madigan Army Medical Center |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 138 |
| Start date | 20 November 2019 |
| Primary completion | 9 July 2021 |
| Estimated completion | 9 July 2021 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Professional nutrition counseling
- No professional nutrition counseling
Conditions studied
- Metabolic Syndrome — all drugs for Metabolic Syndrome →
Sponsor
Madigan Army Medical Center
Who can join
Adults 18 to 45, any sex, with Metabolic Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A prospective, randomized, controlled trial enrolling up to 150 service members (SMs) from two sites; Joint Base Lewis McChord (JBLM) in the Northwest and Joint Base San Antonio (JBSA)-Lackland in the Southwest. A baseline genomic profile (70 genes/80 single nucleotide polymorphisms \[SNPs\]) augmented by common serum biomarkers specific to diet-related chronic disease (metabolic syndrome, cardiovascular disease \[CVD\], vitamin D deficiency) risk will be created. Subjects will be randomized to either personalized nutrition counseling or standard nutrition education for 6 weeks. This interval matches Service-run healthy weight initiatives such as the Army's current Fit for Performance Program. To promote self-care and engagement, a digital app will be utilized for 2 weeks for real-time health data capture with continuous feedback and will be validated with in-person RD interviews. Physical activity and injury data, sun exposure, and family history will help elucidate unique individual responses. Participant follow-up at 12 weeks will evaluate changes in anthropometrics and metabolic, cardiovascular, and vitamin D biomarkers.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04959318
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Madigan Army Medical Center trials
Trials by the same sponsor.
- NCT07335276 — Enhancing Operational Readiness With Digital Self-Managed Cognitive Behavioral Therapy for Insomnia (CBTI) · NA · not yet recruiting
- NCT05190341 — Ibuprofen Versus Ketorolac for Pain Relief During Hysterosalpingogram · Phase 4 · terminated
- NCT04704297 — Trigger Point Injection for Myofascial Pain Syndrome in the Low Back: A Randomized Controlled Trial · Phase 4 · recruiting
- NCT04547413 — STI/HIV Intervention Behavioral Intervention Program · NA · completed
- NCT04556136 — Comparing a Novel Phototherapy Kiosk to Oral Vitamin D Supplementation · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04959318 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Madigan Army Medical Center
- Last refreshed: 11 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04959318.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing