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Adult Broad Learning Experiment (ABLE): Feasibility Study

Adult Broad Learning Experiment (ABLE): Feasibility Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03438136
Acronym
ABLE
Enrollment
22
Registered
2018-02-19
Start date
2017-12-05
Completion date
2019-12-13
Last updated
2018-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Decline

Brief summary

This study evaluates the feasibility of enrolling and retaining older adults in a 15-week intervention that will implement six factors from early childhood experiences: individualized scaffolding (having a responsive teacher), forgiving environment (allowing the learner to make and learn from mistakes), growth mindset (believing that abilities can develop with effort), open-minded learning (exploring new experiences), serious commitment to learning (adopting a learning lifestyle), and learning multiple skills simultaneously. These six factors will be implemented via concurrent classes at the UCR Extension center (OSHER Lifelong Learning Institute).

Interventions

BEHAVIORALAdult Broad Learning Experiment (ABLE)

This intervention implements six factors from early childhood experiences: individualized scaffolding (having a responsive teacher), forgiving environment (allowing the learner to make and learn from mistakes), growth mindset (believing that abilities can develop with effort), open-minded learning (exploring new experiences), serious commitment to learning (adopting a learning lifestyle), and learning multiple skills simultaneously.

Sponsors

American Psychological Foundation
CollaboratorOTHER
University of California, Riverside
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Half of the participants will participate in the intervention, and the other half will be assigned to a no contact control group.

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 55 years of age or older * Fluent in English * Have not been diagnosed with a cognitive condition (e.g., Mild Cognitive Impairment, Alzheimer's, and Dementia) * Currently not experiencing a mental health disorder (e.g., anxiety, depression, Schizophrenia) * Have normal eye vision or corrected-to-normal eye vision * Not proficient in any of the three skills that will be taught during the intervention. Proficiency of skills will be determined by participants' self-report of their experience with each skill. Only potential participants who self-report having less than one or more years of experience with any of the three skills in the past 10 years or as having less than 5 years of experience more than 50 years ago will be considered as being unfamiliar with that skill (or skills) and will be qualified to participate in the study.

Exclusion criteria

n/a

Design outcomes

Primary

MeasureTime frameDescription
Screening-to-enrollment ratioBeginning of the intervention (Week 1)Number of participants we screen relative to the number of participants who enroll
Intervention adherenceThroughout the intervention (15 weeks)Amount of homework hours logged and class attendance
Enjoyment of intervention activitiesWeek 15Assessed via a brief questionnaire of 4 questions created by our research team. Range: 4-24, summed across 4 questions.

Secondary

MeasureTime frameDescription
Executive FunctionPre-test to post-test (15 weeks: Week 1; Week 15)Measured by NIH EXAMINER battery
Broad Learning Adult QuestionnairePre-test to post-test (15 weeks: Week 1; Week 15)New questionnaire developed by PI

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026