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NCT04497974
Sweet Tooth: Nature or Nurture? Role of Long-term Dietary Sweetness Exposure on Sweetness Preferences
NA trial testing Dietary intervention in Food Preferences in 180 participants. Completed in 5 June 2024.
5 June 2024
Quick facts
| Lead sponsor | Wageningen University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | basic science |
| Enrollment | 180 |
| Start date | 20 October 2020 |
| Primary completion | 5 June 2024 |
| Estimated completion | 5 June 2024 |
| Sites | 1 location across Netherlands |
Drugs / interventions tested
- Dietary intervention
Conditions studied
- Food Preferences — all drugs for Food Preferences →
Sponsor
Wageningen University
Who can join
Adults 18 to 65, any sex, with Food Preferences. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In recent years, social pressure has been exerted towards lowering sugar and sweetness levels in foods, with the aim of decreasing the sweetness preference of the general population. However, the resilience/flexibility of sweetness preferences and the impact on energy intake is a fundamental knowledge gap. Recent, relatively long-term studies limited to no more than 3 months did not find a relationship between sweetness exposure and sweetness preferences. Therefore, a longer-term systematic investigation is necessary to objectively evaluate whether sweetness preferences can be altered via varying the sweetness exposure and whether it can affect other outcomes, such as perceived taste intensity, food intake, body weight, body composition, glucose homeostasis and sweet liker type. The study sample will consist of 180 subjects. Enrolled participants will be distributed into three intervention groups; regular dietary sweetness exposure (n=60); low dietary sweetness exposure (n=60); and high dietary sweetness exposure (n =60). The intervention is semi-controlled for a period of six months. Preference and perceived taste intensity of a series of familiar and unfamiliar foods will be assessed at baseline (Day 0), during the intervention (Month 1, Month 3, Month 6) and in the follow-up period (Month 7, Month 10). Furthermore, outcomes such as observed food choice and intake during a test meal, reported food preferences, reported food cravings, sweet-liker type, glucose homeostasis, body weight, body composition and biomarkers related to diabetes and cardiovascular disease will be assessed as well.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
Study protocol of the sweet tooth study, randomized controlled trial with partial food provision on the effect of low, regular and high dietary sweetness exposure on sweetness preferences in Dutch adults.
Čad EM, Tang CS, de Jong HBT, Mars M, et al · · 2023 · cited 10× · PMID 36627602 · DOI 10.1186/s12889-022-14946-4 -
Understanding the determinants of sweet taste liking in the African and East Asian ancestry groups in the U.S.-A study protocol.
Cheung MM, Hubert PA, Reed DR, Pouget ER, et al · · 2024 · cited 5× · PMID 38683826 · DOI 10.1371/journal.pone.0300071 -
The Sweet Tooth Trial: A Parallel Randomized Controlled Trial Investigating the Effects of A 6-Month Low, Regular, or High Dietary Sweet Taste Exposure on Sweet Taste Liking, and Various Outcomes Related to Food Intake and Weight Status.
Čad EM, Mars M, Pretorius L, van der Kruijssen M, et al · · 2026 · cited 2× · PMID 41485871 · DOI 10.1016/j.ajcnut.2025.09.041 -
XXXIIIth Annual Meeting of the European Chemoreception Research Organization, ECRO 2023, “Diverse Flavors” Van der Valk Hotel Nijmegen Lent, The Netherlands, 18 - 21 September 2023
· 2023
Verify or expand the search:
- PubMed search for NCT04497974
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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 NCT04497974 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Wageningen University
- Last refreshed: 13 June 2024
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/NCT04497974.
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