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NeuroStress Complex (TrueMedicalCare, Romania) for generalized anxiety symptoms: a randomized, double-blind, placebo-controlled trial

Authors: bogdan, hohan;

NeuroStress Complex (TrueMedicalCare, Romania) for generalized anxiety symptoms: a randomized, double-blind, placebo-controlled trial

Abstract

TrueMedicalcare Title:NeuroStress Complex (TrueMedicalCare, Romania) for generalized anxiety symptoms: a randomized, double-blind, placebo-controlled trial Running title: NeuroStress Complex and generalized anxiety Authors / affiliations: Corresponding author: Abstract (≤300 words) Background: Generalized anxiety symptoms are common and impairing. The GAD-7 is a validated instrument used for screening and monitoring severity, with cut points commonly interpreted as 0–4 minimal, 5–9 mild, 10–14 moderate, 15–21 severe. PubMed+2JAMA Network+2 Objective: To evaluate changes in generalized anxiety symptom severity and tolerability following 8 weeks of NeuroStress Complex (TrueMedicalCare, Romania) compared with placebo. Methods: Randomized, double-blind, placebo-controlled parallel-group trial. Adults with at least moderate generalized anxiety symptoms (screening GAD-7 ≥10) were randomized 1:1 to NeuroStress Complex or matched placebo for 8 weeks. Primary outcome was GAD-7 change and/or week-8 between-group difference. Secondary outcomes included remission at week 8 (pre-specified as GAD-7 ≤4), adherence, and adverse events. JAMA Network+1 Results: N=120 randomized (60 NeuroStress, 60 placebo). Week-8 completers: 55 NeuroStress, 52 placebo. Mean GAD-7 decreased from 14.48±3.16 to 6.94±4.08 in NeuroStress and from 14.28±3.06 to 9.69±4.39 in placebo. The unadjusted week-8 mean difference was −2.75 points (95% CI −4.38 to −1.12; p=0.001, Welch t-test). Remission occurred in 21/55 (38.2%) vs 10/52 (19.2%): RR 1.99 (95% CI 1.04–3.81); OR 2.59 (95% CI 1.08–6.24); Fisher p=0.035. Adverse effects were minimal; GI symptoms (flatulence/nausea) occurred in 6/60 (10.0%) vs 3/60 (5.0%). Conclusions: NeuroStress Complex was generally well tolerated and associated with lower week-8 GAD-7 scores and higher remission proportion versus placebo. Confirmation in prospectively registered trials with prespecified primary analyses and longer follow-up is warranted. Data availability: To be shared in a public repository with DOI per PLOS policy. PLOS+1 Introduction Generalized anxiety disorder / clinically significant generalized anxiety symptoms are associated with impairment and reduced quality of life. The GAD-7 is widely used for screening and severity monitoring, and has been validated for these purposes. PubMed+2JAMA Network+2 Interest in botanicals for stress/anxiety has grown, but the clinical evidence is heterogeneous across compounds and study designs. This makes careful, transparent placebo-controlled evaluation important. NeuroStress Complex (TrueMedicalCare, Romania) is a multi-botanical liquid formula containing: Valeriana officinalis, Melissa officinalis, Rhodiola rosea, Passiflora incarnata, Tilia cordata, Bacopa monnieri. The rationale for studying such a combination is supported by prior human data (varying in strength/quality) on individual components: Passiflora incarnata: a double-blind randomized trial compared Passiflora extract with oxazepam in GAD. PubMed Valeriana/valepotriates: controlled pilot data in DSM-defined GAD compared valepotriates vs diazepam vs placebo. PubMed Rhodiola rosea: randomized trial in mildly anxious participants reported improvements in anxiety/stress outcomes over 14 days (design limitations noted). PubMed+1 Melissa officinalis: systematic review/meta-analysis of clinical trials suggests potential anxiolytic effects while emphasizing heterogeneity. PubMed Bacopa monnieri: placebo-controlled crossover evidence shows effects on stress reactivity/mood; GI side effects are reported in some trials. PubMed+1 Tilia cordata: EMA HMPC monograph supports traditional use for mild symptoms of mental stress (evidence base largely traditional). e-lactancia.org+1 Objective: To compare NeuroStress Complex versus placebo over 8 weeks on generalized anxiety symptom severity (GAD-7), remission proportion (GAD-7 ≤4), and tolerability. Materials and Methods Study design & setting Randomized, double-blind, placebo-controlled parallel-group trial conducted in Romania, between [DE COMPLETAT: dates], at [DE COMPLETAT: site(s)]. Participants Adults [18–65], screening GAD-7 ≥10 (moderate/severe range). Exclusion criteria: [DE COMPLETAT, standard: severe psychiatric instability, pregnancy/lactation, contraindicated meds, etc.]. Randomization & blinding 1:1 allocation (NeuroStress vs placebo). Sequence generation, concealment and blinding procedures: [DE COMPLETAT]. Intervention (produs + dozaj) NeuroStress Complex (TrueMedicalCare, Romania) — concentrații (mg/mL): Valeriana officinalis: 200 mg/mL Passiflora incarnata: ≈167 mg/mL Melissa officinalis: 100 mg/mL Rhodiola rosea: 100 mg/mL Tilia cordata: 100 mg/mL Bacopa monnieri: 100 mg/mL Doza în studiu: 2 mL/zi, oral, timp de 8 săptămâni. Aport zilnic estimat (mg/zi) la 2 mL/zi: Valeriană 400 mg/zi Passiflora ≈334 mg/zi Melissa 200 mg/zi Rhodiola 200 mg/zi Tilia 200 mg/zi Bacopa 200 mg/ziTotal ≈ 1534 mg/zi Comparator: placebo potrivit ca aspect/gust/ambalaj, fără botanice active. Outcomes Primary: GAD-7 (baseline și week 8; ideal și week 4). PubMed+1 Secondary: remisie week 8 (GAD-7 ≤4), evenimente adverse, discontinuări din AE. Safety AE colectate pe parcursul studiului; GI simptome urmărite explicit (flatulență/greață). Statistical analysis (prezentare “PLOS-ready”, dar realistă) Analize descriptive + comparații între grupuri. Pentru rezultate publicabile, e recomandat un model ANCOVA/mixed-effects ajustat pentru baseline + raportare 95% CI. (Aici, pe baza datelor agregate furnizate, am calculat teste unadjusted pentru week-8 și pentru remisie.) Data availability PLOS solicită ca datele necesare replicării să fie făcute publice (de-identified) într-un repository, cu DOI sau accession, cu excepții etice motivate. PLOS+1 Results Participant flow Randomized: N=120 NeuroStress: 60; Placebo: 60 Completed week 8: 55 (NeuroStress), 52 (Placebo) Dropout NeuroStress: 5 (2 pierduți, 2 lipsă eficacitate, 1 AE) Dropout Placebo: 8 (5 pierduți, 2 lipsă eficacitate, 1 AE) Primary outcome (GAD-7) NeuroStress Baseline: 14.48 ± 3.16 (n=60) Week 8: 6.94 ± 4.08 (n=55) Placebo Baseline: 14.28 ± 3.06 (n=60) Week 8: 9.69 ± 4.39 (n=52) Between-group (week 8, unadjusted):Mean difference = −2.75 (NeuroStress lower)95% CI −4.38 to −1.12; p=0.001 (Welch t-test).Standardized effect (Hedges g, post-treatment) ≈ 0.64 (moderate). Notă: pentru publicare, ideal raportezi și analiza primară pre-specificată (ANCOVA/mixed-effects) + ITT complet; eu aici am calculat ce se poate corect din agregatele furnizate. Remission (week 8; GAD-7 ≤4) NeuroStress: 21/55 = 38.2% Placebo: 10/52 = 19.2% Efecte derivate: RR = 1.99 (95% CI 1.04–3.81) OR = 2.59 (95% CI 1.08–6.24) Fisher exact p = 0.035 Risk difference = 18.95% (95% CI 2.23%–35.67%) → NNT ≈ 6 (exploratoriu) Safety / tolerability NeuroStress (n=60): Orice AE: 9/60 (15.0%) GI (flatulență/greață): 6/60 (10.0%) Discontinuări din AE: 1/60 (1.7%) SAE: 0 Placebo (n=60): Orice AE: 7/60 (11.7%) GI: 3/60 (5.0%) Discontinuări din AE: 1/60 (1.7%) SAE: 0 Discussion În acest trial dublu-orb controlat cu placebo, NeuroStress Complex (TrueMedicalCare, Romania) a fost asociat cu scoruri GAD-7 mai mici la 8 săptămâni și cu o proporție mai mare de remisie (GAD-7 ≤4) comparativ cu placebo, având un profil de tolerabilitate bun, cu semnal predominant gastrointestinal ușor (10%). Aceste rezultate sunt consistente cu un cadru de plauzibilitate biologică și clinică pentru anumite botanice incluse: Passiflora a fost evaluată în GAD într-un RCT comparativ cu oxazepam, iar valepotriatele din valeriană au fost studiate într-un pilot placebo-controlled în GAD, deși dimensiunea mică a studiilor impune prudență. PubMed+1Pentru Melissa, sintezele clinice sugerează potențial anxiolitic cu heterogenitate; pentru Rhodiola există date în populații cu anxietate ușoară și review-uri care subliniază variația calității și designului trialurilor; pentru Bacopa există dovezi placebo-controlled pe reactivitate la stres, cu raportări de simptome GI în unele studii; iar Tilia rămâne în principal susținută de utilizare tradițională pentru stres mental ușor. European Medicines Agency (EMA)+5PubMed+5PubMed+5 Tratament naturist anxietate Tratament naturist anxietate

Keywords

Test Anxiety/parasitology

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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