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Memory and Fear Study (Fear of Memory Loss Study)

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Northwestern University

Status

Completed

Conditions

Anxiety and Fear

Treatments

Behavioral: Conventional Mindfulness Program
Behavioral: Tailored Mindfulness Program for Fear of Memory Loss

Study type

Interventional

Funder types

Other

Identifiers

NCT04821960
STU00214078

Details and patient eligibility

About

This study is a randomized control study to determine the impact of a tailored, web-based mindfulness program to reduce anxiety and increase the quality of life in older adults experiencing dementia-related fears, relative to a conventional meditation program.

Full description

The study will test two different types of online mindfulness programs to see if an online self-paced mindfulness program can help reduce anxiety related to memory loss. Participants will be involved in the study for a total of 10 weeks. Participants will log on to an online mindfulness program 4 days per week for about 10-20 minutes each. The total program will last 3 weeks. Participants will also be asked to complete questionnaires before starting the program, during the program, and after they complete the program.

Enrollment

81 patients

Sex

All

Ages

55+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 55 years of age or older
  • Elevated dementia-related fear
  • Able to read/write in English
  • Willingness to be randomized to intervention group
  • Willingness to complete three weeks of self-guided intervention, questionnaires, and cognitive tests.
  • Access to a reliable internet connection

Exclusion criteria

  • Diagnosis of mild cognitive impairment, Alzheimer's Disease, or dementia by a healthcare provider.
  • Impaired cognitive or neurologic function
  • Unstable medical condition
  • Severe depression
  • Current treatment for anxiety or depression
  • Current participation in another psychotherapy
  • Current use of psychiatric medication
  • Current substance use disorder
  • Inadequate vision or hearing to interact with study materials

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

81 participants in 2 patient groups

Conventional Mindfulness Program
Active Comparator group
Description:
Routine mindfulness lessons and activities.
Treatment:
Behavioral: Conventional Mindfulness Program
Tailored Mindfulness Program for Fear of Memory Loss
Experimental group
Description:
Tailored mindfulness lessons and activities for fear of memory loss.
Treatment:
Behavioral: Tailored Mindfulness Program for Fear of Memory Loss

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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