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Post-ICU Problem Solving for Cognitive Impairment (PIC-UPS Trial)
N/A
Waitlist Available
Led By Judith A Tate, PhD
Research Sponsored by Ohio State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 15 months
Awards & highlights
PIC-UPS Trial Summary
This trial will test a program to help ICU patients with cognitive problems from their critical illness. It will study how well the program works and if patients want to do it.
Eligible Conditions
- Cognitive Impairment
- Mechanical Ventilation Complication
- Critical Illness
- Delirium
PIC-UPS Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 15 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~15 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Access change in participant use of the health system
Assess change in functional independence when performing activities of daily living as measured by the Katz Activities of Daily Living Scale.
Assess change in functional independence when performing instrumental activities of daily living using the Lawton Instrumental Activities of Daily Living.
+8 morePIC-UPS Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Post-ICU Problem SolvingExperimental Treatment1 Intervention
The PIC-UPS intervention focuses on self-regulation activities and environmental cues to overcome problems with memory, planning and decision-making. The interventionist uses guided discovery, reviews progress, and emphasizes generalization and transfer to other patient-identified problems. This approach may be more acceptable to participants because they can see the relevance of tasks to everyday life. Activities such as goal-setting, self-evaluation and reflective thinking behaviors enhance self-efficacy and increase the likelihood that the individual will engage in self-management behaviors. The first session of PIC-UPS will be delivered after enrollment to those participants randomized to the intervention group. Weekly intervention sessions will be conducted by a trained interventionist and supplemented by telephone reminders to complete daily homework. Follow-up data collection will be conducted in the home by a blinded data collector three months post-enrollment.
Group II: Control GroupActive Control1 Intervention
Participants in the control group will complete several surveys upon enrollment and randomization. Follow-up data collection will be conducted in the home for all participants control group by a blinded data collector three months post-enrollment.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Post-ICU Problem Solving
2022
N/A
~20
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Who is running the clinical trial?
Ohio State UniversityLead Sponsor
837 Previous Clinical Trials
507,927 Total Patients Enrolled
Judith A Tate, PhDPrincipal InvestigatorOhio State University
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Research Study Groups:
This trial has the following groups:- Group 1: Control Group
- Group 2: Post-ICU Problem Solving
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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