StackTerminal.Health

Your personalized stack

Public 2/9/2026

Built from your goals and the supplement evidence library. You can edit doses and timing.

Practical pre-check
Deterministic heuristics (stimulants, duplicates, hydration). Not medical advice.
Supplements
6
Items in this stack
Training load
Unknown load
Need more wearable data
Stimulant estimate
200 mg
Only counts explicit caffeine items
STIMULANT LOAD
Stimulant load
Estimated caffeine dose is about 200mg/day (only counting explicit caffeine items). This can shift sleep and perceived recovery, especially under higher training load.
AI risk assessment
Context: No wearable data
No assessment yet.
Supplements
6 items
Morning or pre-workout • Caffeine anhydrous • Click to expand
Caffeine acutely improves multiple performance outcomes; common effective range is ~3–6 mg/kg in many studies, with high inter-individual variability.
200mg
Sleep disruption (safety warning)
High
Population: Healthy adults
Study type: Systematic review & meta-analysis
Dose context: 200 mg typical (range: 100–400 mg) • Duration: Acute

Caffeine prolongs sleep latency, reduces total sleep time and efficiency; clinically meaningful disruption occurs with 400 mg within 8–12 h of bedtime.

Citation: Gardiner C et al. Sleep Med Rev. 2023;68:101764.DOI: 10.1016/j.smrv.2022.101764https://pubmed.ncbi.nlm.nih.gov/36870101/
Avoid caffeine within 6–8 h of intended sleep time when sleep is a priority.
Cognitive performance (attention, reaction time)
High
Population: Healthy adults (31 trials, n=1,455)
Study type: Systematic review & meta-analysis
Dose context: 200 mg typical (range: 100–400 mg) • Duration: Acute

Caffeine significantly improves reaction time (g=0.28) and accuracy (g=0.27) on attention tasks; dose ≥200 mg shows larger effects.

Citation: Grgic J et al. Int J Sport Nutr Exerc Metab. 2021;31(3):199–206.https://pubmed.ncbi.nlm.nih.gov/33800853/
Benefits are acute; tolerance develops with daily use.
Endurance and sport performance
High
Population: Athletes and active adults
Study type: ISSN Position Stand (systematic review)
Dose context: 200 mg typical (range: 100–400 mg) • Duration: Acute (single dose)

Strong evidence that 3–6 mg/kg caffeine improves endurance, strength, and power; benefits consistent but moderated by genetics and habituation.

Citation: Guest NS et al. J Int Soc Sports Nutr. 2021;18(1):1.DOI: 10.1186/s12970-020-00383-4https://pubmed.ncbi.nlm.nih.gov/33388079/
CYP1A2 and ADORA2A genotypes influence individual response.
Beta-AlanineModerate
Evening • Beta-alanine • Click to expand
Chronic beta-alanine supplementation increases muscle carnosine and can improve performance, commonly using multi-gram daily dosing over weeks.
3200mg
Exercise capacity and performance (broader meta-analysis)
Moderate
Population: Mixed athletes; 1,461 participants across 40 studies
Study type: Systematic review & meta-analysis
Dose context: 4800 mg typical (range: 3200–6400 mg) • Duration: 4–12 weeks

Significant overall effect size (ES = 0.18, 95% CI 0.08–0.28); greatest benefit for exercise in 1–10 min duration window.

Citation: Saunders B et al. Br J Sports Med. 2017;51(8):658–669.DOI: 10.1136/bjsports-2016-096396https://pubmed.ncbi.nlm.nih.gov/27797728/
Effect size modest; larger in capacity vs. performance measures.
High-intensity exercise performance (1–4 min efforts) via muscle carnosine elevation
High
Population: Athletes and trained adults
Study type: ISSN Position Stand (systematic review)
Dose context: 4800 mg typical (range: 3200–6400 mg) • Duration: 4–12 weeks

4–6 g/day for ≥4 weeks significantly augments muscle carnosine (intracellular pH buffer) and improves exercise lasting 1–4 min; no benefit for efforts <60 s.

Citation: Trexler ET et al. J Int Soc Sports Nutr. 2015;12:30.DOI: 10.1186/s12970-015-0090-yhttps://pubmed.ncbi.nlm.nih.gov/26175657/
Paresthesia (tingling) is common but harmless; split dosing reduces it.
Evening • Cholecalciferol • Click to expand
Effectively raises serum 25(OH)D concentrations.
50mg
Vitamin D status and physical performance in athletes
Low
Population: Competitive and recreational athletes
Study type: Narrative review
Dose context:

Vitamin D insufficiency is prevalent among athletes, particularly indoor athletes and those in northern latitudes in winter. Insufficiency is associated with reduced muscle strength, power, and endurance; supplementation of 2,000–6,000 IU/day recommended to maintain 25(OH)D >40 ng/mL.

Citation: Yoon S, Kwon O, Kim J. Vitamin D in athletes: focus on physical performance and musculoskeletal injuries. Phys Act Nutr. 2021;25(2):20-25.DOI: 10.20463/pan.2021.0011https://pubmed.ncbi.nlm.nih.gov/34315203/
Narrative review; prevalence data robust, intervention evidence more limited.
Fracture prevention in elderly adults
Moderate
Population: Ambulatory and institutionalized elderly persons
Study type: Systematic review and meta-analysis of RCTs
Dose context:

Vitamin D at 700–800 IU/day reduced hip fracture risk by 26% (RR 0.74) and any nonvertebral fracture by 23% (RR 0.77); no significant benefit was observed at 400 IU/day.

Citation: Bischoff-Ferrari HA, Willett WC, Wong JB, et al. Fracture prevention with vitamin D supplementation: a meta-analysis of randomized controlled trials. JAMA. 2005;293(18):2257-64.DOI: 10.1001/jama.293.18.2257https://pubmed.ncbi.nlm.nih.gov/15886381/
Dose-dependent effect; 400 IU/day insufficient for fracture prevention.
Prevention of acute respiratory tract infections
Moderate
Population: Children and adults (ages 0–95); 25 RCTs, n=11,321
Study type: Systematic review and meta-analysis of individual participant data from RCTs
Dose context:

Vitamin D supplementation reduced risk of acute respiratory tract infection (adjusted OR 0.88, 95% CI 0.81–0.96); greatest benefit in those with baseline deficiency (<25 nmol/L) and those receiving daily or weekly dosing rather than bolus doses.

Citation: Martineau AR, Jolliffe DA, Hooper RL, et al. Vitamin D supplementation to prevent acute respiratory tract infections: systematic review and meta-analysis of individual participant data. BMJ. 2017;356:i6583.DOI: 10.1136/bmj.i6583https://pubmed.ncbi.nlm.nih.gov/28202713/
IPD meta-analysis; high statistical power; effect strongest in vitamin D-deficient individuals.
Evening • Creatine monohydrate • Click to expand
Creatine monohydrate is safe and effective for improving performance and lean mass at commonly used doses.
5500mg
Strength / power performance
High
Population: Healthy adults; athletes and recreationally trained
Study type: ISSN Position Stand (comprehensive review)
Dose context: 5000 mg typical (range: 3000–5000 mg) • Duration: 4–12+ weeks

Consistent improvements in strength, power, and training volume; safe for long-term use (up to 30 g/day for 5 years studied). Loading optional; maintenance commonly 3–5 g/day.

Citation: Kreider RB et al. J Int Soc Sports Nutr. 2017;14:18.DOI: 10.1186/s12970-017-0173-zhttps://pubmed.ncbi.nlm.nih.gov/28615996/
Non-responders (~25–30%) exist; vegetarians/vegans tend to show larger gains.
Short-term memory and reasoning
Moderate
Population: Healthy adults (6 RCTs, n=281); larger effects in older adults
Study type: Systematic review of RCTs
Dose context: 5000 mg typical (range: 3000–20000 mg) • Duration: 4–12 weeks

Oral creatine may improve short-term memory and intelligence/reasoning in healthy individuals; effect on other cognitive domains unclear.

Citation: Avgerinos KI et al. Exp Gerontol. 2018;108:166–173.DOI: 10.1016/j.exger.2018.04.013https://pubmed.ncbi.nlm.nih.gov/29704637/
Cognitive benefits most consistent in aging or sleep-deprived populations and those with lower dietary creatine (e.g., vegetarians).
Evening • Triglyceride fish oil • Click to expand
Improves triglycerides and other risk markers; outcomes depend on baseline risk and dose.
2000mg
Cardiovascular outcomes and mortality
Moderate
Population: General adults and cardiovascular risk populations
Study type: Systematic review and meta-analysis
Dose context:

Omega-3 supplementation associated with reductions in cardiovascular events; benefit most consistent at higher EPA+DHA doses (≥2 g/day) and in high-risk populations.

Citation: See Omega-3 cardiovascular outcome trials meta-analysis.https://pmc.ncbi.nlm.nih.gov/articles/PMC12129820/
PMC full-text review; curated cardiovascular evidence.
Delayed-onset muscle soreness (DOMS) after eccentric exercise
Low
Population: Healthy adults performing eccentric exercise
Study type: Systematic review and meta-analysis of RCTs
Dose context:

Omega-3 PUFA supplementation produced a statistically significant reduction in DOMS (MD −0.93, 95% CI −1.44 to −0.42; p=0.0004) across 12 RCTs, though the effect size fell below the minimal clinically important difference of 1.4 on a 10-point VAS. Low-quality evidence overall.

Citation: Lv ZT, Zhang JM, Zhu WT. Omega-3 Polyunsaturated Fatty Acid Supplementation for Reducing Muscle Soreness after Eccentric Exercise: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Biomed Res Int. 2020;2020:8062017.DOI: 10.1155/2020/8062017https://pubmed.ncbi.nlm.nih.gov/32382573/
Statistical significance without clear clinical significance; larger doses (≥6 g/day) and longer supplementation (≥7 weeks) may be required.
Triglyceride reduction
High
Population: Adults with hypertriglyceridemia
Study type: Systematic review and meta-analysis of RCTs
Dose context: (range: 2000–4000 mg)

High-dose omega-3 (≥2 g EPA+DHA/day) consistently reduces fasting triglycerides by 15–30% in adults with elevated baseline levels.

Citation: See PubMed triglyceride meta-analysis.https://pubmed.ncbi.nlm.nih.gov/34139241/
Evening • Lyophilized powder • Click to expand
Retatrutide produced large, dose-dependent mean body-weight reductions over 48 weeks versus placebo; GI adverse effects were common and dose-related.
12mg
Body weight reduction
High
Population: Adults with obesity (without diabetes) in a randomized controlled phase 2 trial
Study type: Randomized, double-blind, placebo-controlled phase 2 trial
Dose context: 12 mg typical (range: 1–12 mg) • Duration: 48 weeks

Retatrutide produced substantial mean body-weight reductions over 48 weeks (up to ~24% at highest dose), with larger losses at higher doses; GI adverse effects were common and dose-related.

Citation: Jastreboff et al., N Engl J Med (2023) — Triple–Hormone-Receptor Agonist Retatrutide for ObesityDOI: 10.1056/NEJMoa2301972https://www.nejm.org/doi/full/10.1056/NEJMoa2301972
Phase 3 registrational program design (TRIUMPH)
Low
Population: Adults with obesity ± OSA, knee osteoarthritis, or cardiovascular disease (>5800 participants across 4 trials)
Study type: Phase 3 registrational program design/rationale publication
Dose context: • Duration: Ongoing (trials projected through 2025–2026)

The TRIUMPH phase 3 program (4 trials, >5800 participants) evaluates once-weekly subcutaneous retatrutide vs. placebo for weight management and obesity-related complications (OSA, OA, CVD). No primary efficacy results published as of early 2026; design and rationale published in 2025.

Citation: Wadden et al., Diabetes Obes Metab (2025) — Retatrutide for obesity, OSA and knee OA: Rationale and design of TRIUMPHhttps://pubmed.ncbi.nlm.nih.gov/41090431/

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