NCT03438136

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).

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2017

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 5, 2017

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 28, 2018

Completed
22 days until next milestone

First Posted

Study publicly available on registry

February 19, 2018

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 13, 2018

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 13, 2019

Completed
Last Updated

February 19, 2018

Status Verified

February 1, 2018

Enrollment Period

1 year

First QC Date

January 28, 2018

Last Update Submit

February 15, 2018

Conditions

Outcome Measures

Primary Outcomes (3)

  • Screening-to-enrollment ratio

    Number of participants we screen relative to the number of participants who enroll

    Beginning of the intervention (Week 1)

  • Intervention adherence

    Amount of homework hours logged and class attendance

    Throughout the intervention (15 weeks)

  • Enjoyment of intervention activities

    Assessed via a brief questionnaire of 4 questions created by our research team. Range: 4-24, summed across 4 questions.

    Week 15

Secondary Outcomes (2)

  • Executive Function

    Pre-test to post-test (15 weeks: Week 1; Week 15)

  • Broad Learning Adult Questionnaire

    Pre-test to post-test (15 weeks: Week 1; Week 15)

Study Arms (2)

Intervention arm

EXPERIMENTAL

This arm will be enrolled in the intervention.

Behavioral: Adult Broad Learning Experiment (ABLE)

No intervention arm

NO INTERVENTION

This arm will be enrolled in a no contact control group.

Interventions

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.

Intervention arm

Eligibility Criteria

Age55 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of California, Riverside

Riverside, California, 92521, United States

Location

MeSH Terms

Conditions

Cognitive Dysfunction

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: Half of the participants will participate in the intervention, and the other half will be assigned to a no contact control group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

January 28, 2018

First Posted

February 19, 2018

Study Start

December 5, 2017

Primary Completion

December 13, 2018

Study Completion

December 13, 2019

Last Updated

February 19, 2018

Record last verified: 2018-02

Locations