Autopsy report · NCT05591794
Effects of Diet Versus Diet Plus Aerobic and Resistant Exercise Program in Overweight Women
Cause of deathStaffing, sites or logistics
“The study was halted prematurely following the departure of two researchers, resulting in insufficient research capacity to continue the study.”
Life of this trial
- Registered 1 month after it had already started.
- Ran for about 2 years 3 months before it stopped.
- 24 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Bezmialem Vakif University
- Sponsor type
- University, hospital or other
- Conditions
- Overweight; Exercise
- Interventions
- Aerobic and resistance exercises; Diet program; Regular walking program
- Participants
- 24
- Sites
- 1
- Countries
- Turkey (Türkiye)
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“The study was stopped because there were not enough eligible patients to complete the study.” - Comparing Palliative Radiotherapy With or Without Carboplatin
“The study was stopped due to insufficient recruitment.” - Involuntary Memories Investigation in Schizophrenia
“The research was stopped because of recruitment difficulties at the end of the study due to a high drop-out rate for one of the two tasks included in the protocol.” - Platelet Reactivity With Fentanyl, Morphine, or no Narcotic
“The study was halted prematurely due to difficulties in recruiting a sufficient number of participants. Despite efforts to enroll eligible individuals, the recruitment goals were not met, making it infeasible to continue the study as planned.” - Function, Pain, and Alignment Following Knee Replacement for the Treatment of Osteoarthritis
“The study was prematurely terminated due to a long pause in study activities and significant missing participant data.”
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.