Last reviewed · How we verify
NCT01717365
Psychometric / Validation Study
trial in To Determine the Psychometric Properties of the Short Child Occupational Profile in 499 participants. Completed.
Quick facts
| Lead sponsor | Texas Woman's University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 499 |
| Sites | 1 location across United States |
Conditions studied
- To Determine the Psychometric Properties of the Short Child Occupational Profile — all drugs for To Determine the Psychometric Properties of the Short Child Occupational Profile →
Sponsor
Texas Woman's University
Who can join
Under 21, any sex, with To Determine the Psychometric Properties of the Short Child Occupational Profile. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Data for the study will be collected from therapist across the world. The therapists will share data they have already compiled from their caseload. Data will be stripped of all personal identifiers and personal health information. The TWU SCOPE research team has no contact with clients whose assessment data is being shared for secondary analysis or clinical data repository. For educational and training purposes clients can be videotaped by the therapist who will obtain consent and/or assent from the client. Not every client will be videotaped. The subjects from the data shared by the therapists are from the ages of 0-21, both male and female, and of any ethnicity. The total amount of data collected from all participating therapists will be 500 pieces.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT01717365
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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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 NCT01717365 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Texas Woman's University
- Last refreshed: 13 October 2017
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/NCT01717365.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing