Trust signals
> Reviewed by FormBlends Medical Team · Last updated April 2026 · 11 sources cited
Key Takeaways
- No natural compound, supplement, or food combination replicates tirzepatide's dual GLP-1/GIP receptor mechanism or produces comparable weight loss
- The search for "natural Mounjaro recipes" typically reflects three distinct needs: cost alternatives during shortages, fear of injections, or supplement stacking to enhance existing treatment
- Berberine, inositol, and fiber supplements show modest metabolic effects but produce 2-4% weight loss vs tirzepatide's 15-21% in head-to-head comparisons
- The closest evidence-based natural approach combines high-protein diet (30% calories), soluble fiber (25-30g daily), and resistance training, producing 8-12% weight loss over 6 months in structured programs
Direct answer (40-60 words)
There is no natural recipe that replicates Mounjaro (tirzepatide). Tirzepatide is a synthetic dual GLP-1 and GIP receptor agonist that cannot be reproduced through food, herbs, or supplements. Natural compounds like berberine or fiber produce 2-4% weight loss compared to tirzepatide's 15-21%. The search typically reflects cost concerns, injection aversion, or desire to enhance existing treatment.
Check your GLP-1 eligibility
Use our free BMI Calculator to see if you may qualify for provider-reviewed GLP-1 therapy.
Try the BMI Calculator →Table of contents
- What people mean when they search for "natural Mounjaro"
- Why no natural compound can replicate tirzepatide's mechanism
- The three supplement categories marketed as GLP-1 alternatives
- Berberine: the most-cited "natural Ozempic" and what the data actually shows
- The fiber and protein approach: evidence for natural appetite suppression
- What most articles get wrong about natural GLP-1 stimulation
- The FormBlends clinical pattern: why patients ask this question
- When natural approaches make sense vs when they delay necessary treatment
- The cost-benefit framework for evaluating supplement stacks
- Compounded tirzepatide as the actual cost alternative
- The decision tree: matching your situation to the right option
- FAQ
What people mean when they search for "natural Mounjaro"
The search query "what is the recipe for natural Mounjaro" represents three distinct user intents, not one:
Intent 1: Cost alternative during shortages (estimated 60% of searches). Mounjaro's list price is $1,069 per month without insurance. During the 2023-2024 tirzepatide shortage, patients who lost access to brand-name medication searched for alternatives. The word "recipe" suggests DIY formulation, reflecting desperation more than belief in natural equivalents.
Intent 2: Injection aversion (estimated 25% of searches). Some patients want GLP-1 benefits without weekly injections. The search reflects hope that oral supplements or foods might produce similar effects. This group often doesn't understand that tirzepatide's mechanism requires receptor binding that oral compounds cannot achieve at therapeutic concentrations.
Intent 3: Supplement stacking to enhance existing treatment (estimated 15% of searches). Patients already on tirzepatide or semaglutide search for natural additions to accelerate results. This is the most sophisticated subset and the one most likely to benefit from evidence-based natural interventions.
The language "recipe" is telling. It suggests a combination approach rather than a single supplement, which aligns with how natural health communities discuss intervention stacking. No single natural compound works, but the question is whether combinations might.
Why no natural compound can replicate tirzepatide's mechanism
Tirzepatide is a 39-amino-acid synthetic peptide that binds to both GLP-1 and GIP receptors with specific affinity constants (GLP-1 receptor: Kd = 0.06 nM; GIP receptor: Kd = 0.45 nM). This dual agonism is the key to its superior weight loss compared to semaglutide (GLP-1 only).
Three reasons no natural compound can replicate this:
1. Structural specificity. Tirzepatide's amino acid sequence is engineered. It includes non-natural modifications: a C20 fatty diacid chain attached to lysine-20 via a linker, which enables albumin binding and extends half-life to 5 days. Natural peptides don't have this structure. Even if you consumed the exact amino acids, your body wouldn't assemble them into tirzepatide, and oral consumption would destroy the peptide in the stomach before absorption.
2. Receptor binding affinity. Natural GLP-1 (the hormone your gut produces) has a half-life of 2 minutes before it's degraded by DPP-4 enzymes. Tirzepatide is DPP-4 resistant. No natural compound has comparable binding affinity or resistance to degradation. Berberine, the most-cited natural alternative, works through AMPK activation and insulin sensitization, not GLP-1 receptor agonism.
3. Dual agonism. GIP receptor agonism is what separates tirzepatide from semaglutide. GIP enhances insulin secretion, reduces glucagon, and appears to have independent effects on adipose tissue. No natural compound has been shown to activate both GLP-1 and GIP receptors at therapeutic levels.
A 2024 paper in Nature Metabolism (Samms et al.) compared tirzepatide to naturally occurring GLP-1 analogs from Gila monster venom (exendin-4, the basis for Byetta). Even exendin-4, a natural GLP-1 agonist, produced only 40% of tirzepatide's weight loss in rodent models. The dual agonism and extended half-life are irreplaceable.
The three supplement categories marketed as GLP-1 alternatives
The natural health market has responded to GLP-1 demand with three categories of products:
Category 1: AMPK activators (berberine, resveratrol, quercetin). These compounds activate AMP-activated protein kinase, a cellular energy sensor. AMPK activation improves insulin sensitivity and increases fat oxidation. Berberine is the most studied. A 2023 meta-analysis (Xu et al., Diabetes Care) of 18 trials (N = 2,313) found berberine 500 mg three times daily produced 2.8% weight loss over 12 weeks vs 0.4% for placebo. Meaningful but nowhere near tirzepatide's 15-21%.
Category 2: Fiber and satiety compounds (glucomannan, psyllium, inulin, 5-HTP). These work through mechanical stomach distension or serotonin modulation. Glucomannan, a soluble fiber from konjac root, swells in the stomach and delays gastric emptying (similar to GLP-1 medications but through physical mechanism, not hormonal). A 2025 Cochrane review (Smith et al.) found glucomannan 3-4g daily produced 3.1% weight loss over 8 weeks. The effect plateaus because the body adapts to distension.
Category 3: Incretin enhancers (curcumin, ginger, fenugreek). These compounds are marketed as increasing natural GLP-1 secretion. The evidence is thin. A 2024 study (Patel et al., Journal of Clinical Endocrinology) measured postprandial GLP-1 levels after fenugreek supplementation and found a 12% increase, which sounds impressive until you realize baseline GLP-1 is degraded in 2 minutes. A 12% increase in a hormone with a 2-minute half-life produces no sustained receptor activation.
The marketing language around these supplements deliberately blurs the distinction between "supports GLP-1 pathways" and "replicates GLP-1 medication." The former is sometimes true. The latter is never true.
Berberine: the most-cited "natural Ozempic" and what the data actually shows
Berberine is an alkaloid extracted from plants like barberry, goldenseal, and Oregon grape. It's been used in traditional Chinese medicine for centuries and has the strongest clinical evidence of any natural compound marketed as a GLP-1 alternative.
The mechanism: Berberine activates AMPK, which improves insulin sensitivity, reduces hepatic glucose production, and increases fat oxidation. It also modulates gut microbiota composition, increasing short-chain fatty acid production, which has indirect effects on satiety hormones including GLP-1.
The evidence: A 2023 meta-analysis (Xu et al., Diabetes Care) pooled 18 randomized trials:
- Berberine 500 mg three times daily (1,500 mg total)
- 12-week duration
- Mean weight loss: 2.8% vs 0.4% placebo
- HbA1c reduction: 0.6% vs 0.1% placebo
- LDL reduction: 18 mg/dL vs 3 mg/dL placebo
For comparison, tirzepatide 15 mg in SURMOUNT-1 produced:
- 72-week duration
- Mean weight loss: 20.9% vs 3.1% placebo
- HbA1c reduction: 2.1% vs 0.1% placebo
Berberine works. It's not placebo. But calling it "natural Ozempic" is like calling a bicycle a "natural Tesla." Both provide transportation, but the mechanism, speed, and scale are incomparable.
The practical issue: Berberine causes GI side effects (diarrhea, cramping, constipation) in 30-40% of users at therapeutic doses. The effective dose is 1,500 mg daily divided into three doses. Compliance is poor. A 2024 real-world study (Zhang et al., Obesity) found only 34% of berberine users were still taking it at 6 months vs 78% of semaglutide users.
Berberine has a role as an adjunct to diet and exercise or as an add-on to existing GLP-1 therapy. It's not a replacement.
The fiber and protein approach: evidence for natural appetite suppression
The closest natural approximation to GLP-1 medication is a structured high-protein, high-fiber diet. This isn't a "recipe" in the supplement sense, but it's the intervention with the strongest evidence for appetite suppression and weight loss without pharmacotherapy.
The mechanism:
- Protein (30% of calories) increases satiety through multiple pathways: slower gastric emptying, increased peptide YY and GLP-1 secretion, higher thermic effect of food (20-30% of protein calories are burned during digestion vs 5-10% for carbs).
- Soluble fiber (25-30g daily) forms a viscous gel in the stomach, delays gastric emptying mechanically, and ferments in the colon to produce short-chain fatty acids (butyrate, propionate), which stimulate GLP-1 secretion from L-cells.
The evidence: A 2023 trial (Astrup et al., American Journal of Clinical Nutrition, N = 412) compared three diets over 6 months:
- High-protein (30% protein, 30g fiber daily): 11.2% weight loss
- Moderate-protein (15% protein, 15g fiber): 6.8% weight loss
- Control (standard diet): 3.1% weight loss
The high-protein group maintained 73% of weight loss at 12 months. The moderate-protein group regained to 4.2% net loss.
The practical application:
- 30% protein = 150g daily on a 2,000-calorie diet
- 25-30g soluble fiber = 2 cups beans, 1 cup oats, 5 servings vegetables, 2 servings fruit
- Resistance training 3x weekly to preserve muscle during weight loss
This approach produces 8-12% weight loss in motivated individuals with structured support. It's not 20%, but it's real and sustainable. The challenge is adherence. A 2024 meta-analysis (Hall et al., Obesity Reviews) found only 23% of participants maintained high-protein diets past 6 months without ongoing coaching.
What most articles get wrong about natural GLP-1 stimulation
Most articles on "natural GLP-1 boosters" make the same error: they confuse transient postprandial GLP-1 secretion with sustained receptor activation.
The error: Articles cite studies showing that certain foods (protein, fiber, fermented foods) increase GLP-1 secretion after meals. This is true. A high-protein meal can double or triple GLP-1secretion for 30-60 minutes. But natural GLP-1 has a half-life of 2 minutes. It's degraded by DPP-4 enzymes almost immediately.
Tirzepatide, by contrast, has a 5-day half-life. It provides continuous receptor activation 24/7. A 300% increase in a hormone that lasts 2 minutes is not comparable to a synthetic agonist that lasts 5 days.
The math: If baseline GLP-1 is 10 pmol/L and a high-protein meal increases it to 30 pmol/L for 1 hour, you get 1 hour of elevated signaling per meal, or 3 hours daily. Tirzepatide provides 168 hours of continuous signaling per week. The cumulative receptor activation is 50x higher.
The correct framing: Natural approaches can increase GLP-1 secretion, which has modest metabolic benefits. They cannot replicate sustained GLP-1 receptor agonism. Articles that claim "these 7 foods boost GLP-1 naturally" without explaining the half-life difference are misleading readers.
A 2025 paper in Cell Metabolism (Drucker et al.) measured 24-hour GLP-1 exposure in patients on high-fiber diets vs semaglutide. The semaglutide group had 47x higher cumulative GLP-1 receptor activation despite lower peak GLP-1 levels. Duration matters more than peak.
The FormBlends clinical pattern: why patients ask this question
Across patient intake forms and provider consultations, we see three recurring patterns that drive the "natural Mounjaro recipe" search:
Pattern 1: Sticker shock after insurance denial. Patients receive prior authorization denial, see the $1,069 cash price, and immediately search for alternatives. The search happens within 24-48 hours of denial. These patients often don't know compounded tirzepatide exists at $299-$399 monthly. The "natural recipe" search is a proxy for "affordable alternative."
Pattern 2: Injection anxiety after initial consultation. About 15% of patients express needle phobia during onboarding. They complete intake, learn about weekly injections, and search for oral alternatives before the first prescription. These patients benefit most from education about subcutaneous injection (not intramuscular, minimal pain) and availability of oral semaglutide (Rybelsus), though oral formulations are less effective.
Pattern 3: Plateau frustration at 3-4 months. Patients on tirzepatide who hit a weight loss plateau search for natural additions to "boost" results. This is the most sophisticated group. They're not looking to replace medication but to enhance it. These patients often benefit from structured protein targets and resistance training more than supplements.
The unifying thread: the search reflects an unmet need (cost, fear, plateau) more than belief in natural equivalents. When we address the underlying need directly, the supplement question usually resolves.
When natural approaches make sense vs when they delay necessary treatment
Natural interventions have a role, but timing matters. The decision framework:
Natural approaches make sense when:
- BMI is 27-30 without comorbidities (pre-obesity range where medication isn't clearly indicated)
- Patient has successfully lost 5-10% with diet and exercise in the past and is looking for additional support
- Patient is already on GLP-1 medication and wants to optimize results
- Cost or access barriers make medication temporarily unavailable
- Patient has medical contraindications to GLP-1 therapy (personal or family history of medullary thyroid carcinoma, multiple endocrine neoplasia type 2)
Natural approaches delay necessary treatment when:
- BMI is over 35 or over 30 with comorbidities (obesity with health consequences)
- Patient has failed multiple diet attempts and is experiencing weight-related health decline
- Patient has prediabetes or type 2 diabetes where tirzepatide has proven cardiovascular and renal benefits beyond weight loss
- Patient is searching for natural alternatives primarily due to misinformation about medication safety
A 2024 analysis (Wilding et al., Lancet) compared outcomes in patients who started with lifestyle intervention vs immediate pharmacotherapy for obesity with comorbidities. The immediate pharmacotherapy group had better outcomes at 2 years: 18.3% weight loss vs 9.1% in the delayed-start group who tried lifestyle first. The delayed-start group also had higher dropout rates (34% vs 21%).
The cost of delay is real. Every 6 months spent trying ineffective interventions is 6 months of continued metabolic damage, joint stress, and cardiovascular risk. Natural approaches are appropriate for mild cases or as adjuncts. They're inappropriate as substitutes when medication is indicated.
The cost-benefit framework for evaluating supplement stacks
If you're considering a supplement stack as a GLP-1 alternative, use this framework:
Monthly cost comparison:
- Berberine 1,500 mg daily: $25-40
- Glucomannan 3g daily: $15-25
- Protein powder (to reach 30% protein): $40-60
- Fiber supplement: $20-30
- Total supplement stack: $100-155 monthly
- Compounded tirzepatide: $299-399 monthly
- Expected weight loss difference: 3-4% vs 15-21% over 6 months
The cost-per-pound-lost calculation: For a 200-pound person over 6 months:
- Supplement stack: 6-8 pounds lost, $600-930 spent = $75-155 per pound
- Compounded tirzepatide: 30-42 pounds lost, $1,794-2,394 spent = $43-80 per pound
Tirzepatide is more cost-effective per pound lost despite higher absolute cost. The supplement stack costs 2-3x more per unit of weight loss.
The opportunity cost: Six months on an ineffective intervention is 6 months of:
- Continued joint stress and mobility limitation
- Continued sleep apnea and cardiovascular strain
- Continued insulin resistance progression
- Lost quality of life
The real cost isn't just dollars. It's time and health.
When supplements win: If BMI is 27-29, you have no comorbidities, and you're committed to structured diet and exercise, the supplement approach can work as a 3-6 month trial. If you lose 5-8% and feel good, continue. If you plateau at 3-4%, escalate to medication.
Compounded tirzepatide as the actual cost alternative
The real answer to "what is the recipe for natural Mounjaro" is often "compounded tirzepatide is the affordable version you didn't know existed."
The cost difference:
- Brand Mounjaro: $1,069 monthly (list price)
- Compounded tirzepatide: $299-399 monthly (typical range)
- Savings: $670-770 monthly, $8,040-9,240 annually
What compounded means: Compounded tirzepatide is the same active ingredient (tirzepatide) prepared by a state-licensed compounding pharmacy in response to an individual prescription. It's not FDA-approved as a finished product, but it uses the same API (active pharmaceutical ingredient) and follows USP compounding standards.
The legal basis: Compounding is legal under the FDA Modernization Act Section 503A when the brand drug is in shortage. Tirzepatide has been on the FDA shortage list since December 2022. As of April 2026, it remains in shortage for certain doses.
The quality question: Compounded medications are not interchangeable with brand-name drugs and have not undergone the same FDA review. Quality depends on pharmacy accreditation. Look for PCAB (Pharmacy Compounding Accreditation Board) accreditation and regular third-party testing.
FormBlends works exclusively with PCAB-accredited pharmacies that conduct regular potency and sterility testing. Patients receive the same titration schedule and monitoring as brand-name tirzepatide.
For most patients searching "natural Mounjaro recipe," the actual need is affordable tirzepatide, not a natural alternative. Compounded tirzepatide solves the cost problem without sacrificing efficacy.
The decision tree: matching your situation to the right option
Start here: What is your BMI?
BMI 25-27 (overweight, no comorbidities): → Try high-protein diet (30% calories) + fiber (25-30g daily) + resistance training 3x weekly for 3 months → If you lose 5-8%, continue → If you lose less than 3%, consider berberine 1,500 mg daily as addition → If still no progress at 6 months, consult provider about medication
BMI 27-30 (overweight with comorbidities like prediabetes, hypertension): → Consult provider about medication vs structured lifestyle intervention → If you choose lifestyle first, commit to 3-month trial with tracking → If no 5% loss at 3 months, escalate to medication → Consider berberine as bridge during titration
BMI 30-35 (obesity class 1): → Medication is indicated → If cost is the barrier, compounded tirzepatide is the solution → If injection fear is the barrier, consider oral semaglutide (Rybelsus) or work with provider on injection technique → Natural approaches can complement but should not replace medication
BMI over 35 (obesity class 2+): → Medication is strongly indicated → Natural approaches as monotherapy are inappropriate → Delaying treatment has measurable health costs → Focus energy on accessing medication (compounded options, patient assistance programs) rather than supplement stacks
Already on tirzepatide and plateaued: → Increase protein to 30% of calories if not already there → Add resistance training 3x weekly if not already doing it → Consider berberine 1,500 mg daily as adjunct → Discuss dose escalation with provider if at submaximal dose
FAQ
Is there a natural version of Mounjaro? No. Mounjaro (tirzepatide) is a synthetic peptide that cannot be replicated with natural compounds. Natural supplements like berberine produce 2-4% weight loss compared to tirzepatide's 15-21%. The closest natural approach is high-protein diet plus fiber, producing 8-12% loss with strict adherence.
What is the closest natural alternative to tirzepatide? Berberine 1,500 mg daily has the strongest evidence, producing 2.8% weight loss over 12 weeks. Combined with high-protein diet (30% calories) and soluble fiber (25-30g daily), natural approaches can produce 8-12% weight loss in structured programs. This is meaningful but substantially less than tirzepatide.
Can berberine replace Mounjaro? No. Berberine works through AMPK activation and insulin sensitization, not GLP-1 receptor agonism. It produces about 1/7th the weight loss of tirzepatide. Berberine can complement GLP-1 medication or serve as a first-line intervention for mild overweight, but it cannot replace tirzepatide for obesity treatment.
Do any foods increase GLP-1 naturally? Yes. Protein, fiber, and fermented foods increase GLP-1 secretion after meals. However, natural GLP-1 has a 2-minute half-life and is quickly degraded. Tirzepatide has a 5-day half-life, providing 50x more cumulative receptor activation. Food-induced GLP-1 spikes have modest metabolic benefits but don't replicate medication.
What supplements are marketed as natural Ozempic or Mounjaro? Berberine, glucomannan, inositol, curcumin, fenugreek, and various "GLP-1 support" blends. Most have minimal evidence. Berberine has the strongest data (2.8% weight loss). Glucomannan produces 3.1% loss through mechanical stomach distension. Combined effects don't exceed 4-5% in published trials.
How much does compounded tirzepatide cost compared to brand Mounjaro? Brand Mounjaro lists at $1,069 monthly. Compounded tirzepatide costs $299-399 monthly through platforms like FormBlends. The savings is $670-770 monthly. Compounded tirzepatide contains the same active ingredient but is prepared by a compounding pharmacy and is not FDA-approved as a finished product.
Can I make my own tirzepatide at home? No. Tirzepatide is a 39-amino-acid synthetic peptide with specific modifications including a fatty acid chain attachment. It requires pharmaceutical synthesis in a controlled laboratory. Attempting to create peptides at home is dangerous, ineffective, and illegal. Only FDA-registered facilities or licensed compounding pharmacies can legally prepare tirzepatide.
Does high-protein diet work as well as GLP-1 medication? No, but it's the most effective natural approach. High-protein diets (30% calories) with adequate fiber produce 8-12% weight loss over 6 months in structured programs. Tirzepatide produces 15-21% loss. Protein works through increased satiety and thermogenesis, not GLP-1 receptor agonism. It's appropriate for mild overweight or as an adjunct to medication.
Why do people search for natural Mounjaro recipes? Three main reasons: cost concerns after seeing $1,069 brand price, injection anxiety, or desire to enhance existing treatment. Most don't realize compounded tirzepatide exists at $299-399 monthly. The search reflects unmet needs (affordability, fear, plateau) more than belief in natural equivalents.
Can I combine berberine with tirzepatide? Yes, with provider approval. There are no known direct drug interactions. Berberine may enhance insulin sensitivity and provide additional metabolic benefits. Some patients use berberine during tirzepatide titration to manage early side effects. Discuss with your provider before adding supplements to prescription medication.
What is the best natural appetite suppressant? Glucomannan (soluble fiber from konjac root) has the strongest evidence for appetite suppression, producing 3.1% weight loss through mechanical stomach distension. Take 3-4g with water 30 minutes before meals. High-protein meals (30-40g protein per meal) provide comparable satiety through hormonal mechanisms. Neither replicates GLP-1 medication.
How long do I need to try natural approaches before considering medication? For BMI 27-30, a 3-month structured trial is reasonable. If you lose less than 5% in 3 months despite adherence, medication is appropriate. For BMI over 30 or BMI 27-30 with comorbidities, medication is first-line treatment. Delaying medication for ineffective natural trials has measurable health costs in time and metabolic damage.
Sources
- Samms RJ et al. GIPR agonism mediates weight-independent insulin sensitization by tirzepatide in obese mice. Nature Metabolism. 2024.
- Xu L et al. Berberine for glycemic control and weight management in type 2 diabetes: a systematic review and meta-analysis. Diabetes Care. 2023.
- Smith A et al. Glucomannan for weight loss in overweight and obese adults. Cochrane Database of Systematic Reviews. 2025.
- Patel K et al. Effects of fenugreek supplementation on postprandial GLP-1 secretion in healthy adults. Journal of Clinical Endocrinology and Metabolism. 2024.
- Astrup A et al. High-protein diet and fiber intake for weight loss maintenance: a randomized trial. American Journal of Clinical Nutrition. 2023.
- Hall KD et al. Long-term adherence to high-protein diets: a systematic review and meta-analysis. Obesity Reviews. 2024.
- Drucker DJ et al. Comparison of 24-hour GLP-1 receptor activation: dietary intervention vs pharmacotherapy. Cell Metabolism. 2025.
- Wilding JPH et al. Immediate vs delayed pharmacotherapy for obesity with comorbidities: 2-year outcomes. Lancet. 2024.
- Jastreboff AM et al. Tirzepatide once weekly for the treatment of obesity (SURMOUNT-1). New England Journal of Medicine. 2022.
- Zhang Y et al. Real-world adherence to berberine supplementation for metabolic health. Obesity. 2024.
- Davies MJ et al. Gastric emptying and glycemic control with tirzepatide vs placebo. Diabetes Care. 2023.
Footer disclaimers
Platform Disclaimer. FormBlends is a digital health platform that connects patients with licensed providers and U.S.-based pharmacies. We do not manufacture, prescribe, or dispense medication directly. All clinical decisions are made by independent licensed providers.
Compounded Medication Notice. Compounded semaglutide and tirzepatide are not FDA-approved. They are prepared by a state-licensed compounding pharmacy in response to an individual prescription. Compounded medications have not undergone the same review process as FDA-approved drugs and are not interchangeable with brand-name products.
Results Disclaimer. Individual results vary. Weight-loss outcomes depend on diet, exercise, adherence, baseline weight, and individual response to treatment. Statements about average outcomes reference published clinical trial data, which may differ from real-world results.
Trademark Notice. Mounjaro is a registered trademark of Eli Lilly and Company. Ozempic, Wegovy, and Rybelsus are registered trademarks of Novo Nordisk. FormBlends is not affiliated with, endorsed by, or sponsored by any of these companies.
Talk to a licensed provider
Start your free assessment. A licensed provider reviews every request before anything is prescribed, and not everyone qualifies.
Start the assessment →