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Sequenced Reverse Recall of Digits--Auditory for Delay Discounting (RehabEF Trial)

N/A
Recruiting
Led By Richard Yi, PhD
Research Sponsored by University of Kansas
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline; week 6-8; month 3; month 6
Awards & highlights

RehabEF Trial Summary

This trial will attempt to reduce unhealthy behaviors in mid-life individuals by training them in executive function skills.

Who is the study for?
This trial is for mid-life individuals in Baltimore neighborhoods willing to join a 5-7 week cognitive training program. It's not for those with severe substance use (except tobacco), major depression, or conditions like traumatic brain injury, dementia, significant learning disabilities, or schizophrenia.Check my eligibility
What is being tested?
The study tests if special memory and verbal exercises can help people make better health decisions by improving their ability to wait for rewards. Participants will do tasks involving recalling words and numbers both visually and audibly.See study design
What are the potential side effects?
Since the interventions are non-medical cognitive training exercises, traditional physical side effects are not expected. However, participants may experience mental fatigue or stress.

RehabEF Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline; week 6-8; month 3; month 6
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline; week 6-8; month 3; month 6 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Delay Discounting (DD)
Secondary outcome measures
Change in Hopkins Verbal Learning Test
Change in Iowa Gambling Task
Change in Letter Numbering Sequencing (LTC)
+1 more
Other outcome measures
Change in Chernyshenko Conscientiousness Scale (CCS)
Change in Patient Activation Measure
Change in The Multidimensional Health Locus of Control
+8 more

RehabEF Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Active Training (AT) GroupExperimental Treatment4 Interventions
Participants will complete four computerized training programs to improve executive function (EF), including Sequenced Recall of Digits - Auditory, Sequenced Reverse Recall of Digits - Auditory, Sequenced Recall of Words - Visual, Verbal Memory - Visual.
Group II: Control Training (CT) GroupActive Control1 Intervention
Participants will complete the four computerized programs relating to executive function (EF), but will be provided with the answer (i.e., without memory requirements). That is, participants in the control condition will not be asked to engage their cognitive functions.

Find a Location

Who is running the clinical trial?

University of Maryland, BaltimoreOTHER
688 Previous Clinical Trials
373,976 Total Patients Enrolled
Michigan State UniversityOTHER
185 Previous Clinical Trials
601,298 Total Patients Enrolled
University of FloridaOTHER
1,340 Previous Clinical Trials
715,025 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

To what demographic is this research opportunity accessible?

"If individuals hope to take part in this research, they must possess a propensity for delay discounting and be within the age range of 40-60. Currently, there are about 432 participants enrolled in the trial."

Answered by AI

Is there currently any recruitment taking place for this medical experiment?

"This experiment, which was initially posted on November 1st 2014 and last adjusted on May 16th 2022, is not actively recruiting participants at this time. However, there are alternative clinical trials that offer enrolment opportunities for prospective patients."

Answered by AI

Are individuals aged 25 and older eligible for enrollment into this clinical trial?

"The upper and lower bounds for patient participation in this trial is determined by age, with the minimum being 40 years old and the maximum 60."

Answered by AI
Recent research and studies
~65 spots leftby Apr 2025