Sleep study for GI cancer surgery patients pulled before starting
NCT ID NCT05044312
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study was designed to track sleep disturbances in adults with gastrointestinal cancers before and after surgery. Participants would have filled out a daily sleep questionnaire and worn a FitBit while in the hospital. However, the study was withdrawn before enrolling anyone, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Expected to start
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Mar 2020
An estimate. Start dates often move.
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adult GI Cancer patients admitted for elective gastrointestinal surgery. 2. Patients with an expected hospitalstay of at least 72 hours. 3. Able to be able to read and speak English. 4. Must have access to internet or use of mobile device for FitBit. Exclusion Criteria: 1. \<18 years of age. 2. Night shift workers. Obtained from job history, any patient \>/= 2 days per week, within the last six months prior consenting, are not eligible.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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