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NCT05194228: Exemplar
Exemplar: Determining the Best Practices for EMA Studies
NA trial testing Ecologial Momentary Assessment settings in Ecological Momentary Assessment Best Practices in 416 participants. Completed in 26 October 2022.
26 October 2022
Quick facts
| Lead sponsor | University of Oklahoma |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | factorial |
| Masking | none |
| Primary purpose | other |
| Enrollment | 416 |
| Start date | 30 November 2021 |
| Primary completion | 26 October 2022 |
| Estimated completion | 26 October 2022 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Ecologial Momentary Assessment settings
Conditions studied
- Ecological Momentary Assessment Best Practices — all drugs for Ecological Momentary Assessment Best Practices →
Sponsor
University of Oklahoma
Who can join
Adults 18 to 99, any sex, with Ecological Momentary Assessment Best Practices. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Ecological momentary assessment (EMA) is a measurement methodology that utilizes the repeated collection of real-time data on participants' behavior and experience in their natural environment. While EMA allows researchers to gain valuable insights into dynamic behavioral processes, the need for frequent self-report can be burdensome and disruptive to participants. Compliance with EMA protocols is important for accurate, unbiased sampling, yet there is no "gold standard" for EMA study design. In the present study, the investigators aim to use a factorial design to identify the optimal components, or combinations of components, for achieving the highest compliance rates for smartphone-based ecological momentary assessments (EMAs). Participants will be randomized into 1 of 32 conditions in a 2x2x2x2x2 design (i.e., number of questions per EMA survey \[15 vs. 25\] x number of EMAs per day \[2 vs. 4\] x EMA prompting schedule \[random vs. fixed times\]) x payment type \[per EMA vs. based on percentage of EMAs completed\] x order of EMA item question types \[i.e., slider type first 2 weeks vs. Likert-type questions first 2 weeks\]). All participants will complete EMAs for 4 weeks. The effect of each factor on EMA compliance will be examined, as well as the effects of interactions on EMA compliance. The investigators will also examine within and between-subjects factors that influence response rates, and 2) contextual features such as environment and mood that may be associated with better compliance and participant engagement. The results of this study will have broad applications for developing best practices guidelines for future studies utilizing EMA methodologies.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
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Mobile Health Interventions for Substance Use Disorders.
Businelle MS, Perski O, Hébert ET, Kendzor DE. · · 2024 · cited 30× · PMID 38346293 · DOI 10.1146/annurev-clinpsy-080822-042337 -
Investigating Best Practices for Ecological Momentary Assessment: Nationwide Factorial Experiment.
Businelle MS, Hébert ET, Shi D, Benson L, et al · · 2024 · cited 16× · PMID 39133915 · DOI 10.2196/50275 -
Detecting Deception and Ensuring Data Integrity in a Nationwide mHealth Randomized Controlled Trial: Factorial Design Survey Study.
Kezbers KM, Robertson MC, Hébert ET, Montgomery A, et al · · 2025 · cited 4× · PMID 39874573 · DOI 10.2196/66384 -
Associations between cannabis use and same-day health and substance use behaviors.
La Torre I, Hébert ET, Kezbers KM, Walters D, et al · · 2025 · cited 3× · PMID 39756126 · DOI 10.1016/j.addbeh.2024.108239 -
Effects of Ecological Momentary Assessment Prompting Schedule on Affect Measurement Variability and Associations With Next-Day Health Behaviors.
Langford JS, Hébert ET, Jones DR, Tonkin SS, et al · · 2026 · PMID 42145270 · DOI 10.1177/10731911261444953
Verify or expand the search:
- PubMed search for NCT05194228
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT05194228 (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 University of Oklahoma
- Last refreshed: 10 January 2023
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/NCT05194228.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing