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NCT03811353
The Turkish Mastication Observation and Evaluation (T-MOE) Instrument
trial testing T-MOE in Chewing Problem in 80 participants. Completed in 19 March 2019.
19 March 2019
Quick facts
| Lead sponsor | Hacettepe University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 80 |
| Start date | 19 February 2019 |
| Primary completion | 19 March 2019 |
| Estimated completion | 19 March 2019 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- T-MOE
Conditions studied
- Chewing Problem — all drugs for Chewing Problem →
- Swallowing Disorder — all drugs for Swallowing Disorder →
Sponsor
Hacettepe University
Who can join
Adults 18 Months to 12, any sex, with Chewing Problem or Swallowing Disorder. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to test the reliability and validity of the T-MOE among pediatric patients with chewing disorders.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Turkish Version of the Mastication Observation and Evaluation (MOE) Instrument: A Reliability and Validity Study in Children.
Serel Arslan S, Demir N, Karaduman AA. · · 2020 · cited 5× · PMID 31292728 · DOI 10.1007/s00455-019-10035-8
Verify or expand the search:
- PubMed search for NCT03811353
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Chewing Problem
Currently open trials in the same condition.
- NCT06491407 — RISK FACTOR ANALYSIS OF CHEWING AND SWALLOWING PERFORMANCE IN GERIATRICS · recruiting
- NCT04458207 — Cognitive Changes and Neural Correlates After Rehabilitation of Masticatory Function in Elderly -an Intervention Study · NA · active not recruiting
Other Hacettepe University trials
Trials by the same sponsor.
- NCT07522060 — Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Us · not yet recruiting
- NCT07390162 — The Effect of Changes in the Frequency of Endotracheal Tube Repositioning in Intensive Care Units on the Prevention of O · NA · not yet recruiting
- NCT07579676 — DEVELOPMENT AND PSYCHOMETRIC EVALUATION OF THE NEUROCOGNITIVE UPPER EXTREMITY TESTS: A RELIABILITY AND VALIDITY STUDY · not yet recruiting
- NCT07524842 — Clinical Performance of Three Different Restorative Materials · NA · not yet recruiting
- NCT07439861 — The Effect of Cognitive Dual-Task on Athletic Performance Parameters in Volleyball Players With and Without Chronic Ankl · not yet recruiting
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 NCT03811353 (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 Hacettepe University
- Last refreshed: 21 March 2019
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/NCT03811353.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing