Yale New Haven Hospital
New Haven, Connecticut, 06520, United States
Location status: Recruiting
NCT Number: NCT06006000
This is a prospective longitudinal study that will evaluate the unmet needs of older adults (65 and older) who return home (either directly or after short-term rehab) after an ICU hospitalization, evaluate the association of these unmet needs with clinically relevant outcomes, and assess barriers and facilitators to addressing these unmet needs. The proposed research will inform the development and evaluation of a subsequent intervention to improve functional outcomes among older ICU survivors, in alignment with the NIH's mission to reduce disability.
Interested in participating?
Request Info65 year and older
All sexes
Observational
New Haven, Connecticut, 06520, United States
Location status: Recruiting
To identify unmet needs in multiple domains after return home from an ICU hospitalization, evaluate whether these unmet needs are associated with disability burden in the subsequent 6 months, and ascertain whether these associations are moderated by initial discharge destination (home or STR).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
PARTICIPANTS
CAREGIVERS
Exclusion criteria
PARTICIPANTS
CAREGIVERS
Time frame: monthly up to 6 months
Number of instances of disability during activities of daily living (ADLs), instrumental activities of daily living (IADLs), and mobility activity. Disability is defined as an inability to complete the task or the need for personal assistance to complete the task. The higher the count, the more disability.
Time frame: monthly up to 6 months
Number of hospital readmissions monthly up to 6 months.
Time frame: monthly up to 6 months
Number of deaths each month up to 6 months.
Time frame: month 6
Barriers and facilitators to addressing unmet needs will be assessed using qualitative interviews. A subgroup of participants will receive qualitative interviews conducted with members of the study team. Content analysis will then be used to identify barriers and facilitators to addressing unmet needs that will be informative when planning a future intervention.
Time frame: monthly up to 6 months
Not returning to the pre-ICU functional baseline within the follow-up period
Interested in participating?
Request InfoYale University
Other
Acronym: LANTERN
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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