Autopsy report · NCT04836533
Enhancing Processing Speed and Executive Functioning in Depressed Older Adults With Computerized Cognitive Training
Cause of deathStaffing, sites or logistics
“Conflicts at the study site prevented the study from being carried out”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 1
- Sponsor
- Queens College, The City University of New York
- Sponsor type
- University, hospital or other
- Conditions
- Depression in Old Age; Depression
- Interventions
- Experimental: Computerized Cognitive Training; Experimental: Open-label antidepressant treatment; Active Comparator: Solitaire Training; Placebo Comparator: Placebo-controlled antidepressant treatment
- Participants
- 0
- Sites
- 1
- Countries
- United States
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“Study was unable to accrue subjects” - Use of Goggle Balloon to Improve Cecal Intubation During Colonoscopy
“no subjects consented due to competing studies” - Identification of Elderly Patients in Need of Palliative Care by Family Physicians
“We were not able to recruit participants to enrol the study. As it was not able, the investigation team decided not to proced.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.