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Behavioural Intervention

Intervention Arm for Mild Cognitive Impairment

N/A
Recruiting
Led By Elizabeth Phelan
Research Sponsored by University of Washington
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Medical record documentation of early dementia and/or depression
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up assessed at 4 weeks post enrollment
Awards & highlights

Study Summary

This trial is testing a tool that helps people learn about safe firearm storage to see if it is practical and if people find it helpful.

Who is the study for?
This trial is for individuals with early signs of dementia or depression who have access to the internet or a mobile device and own firearms. It's not suitable for those currently having thoughts of suicide.Check my eligibility
What is being tested?
The study is examining a decision aid designed to help people make choices about safe firearm storage, particularly in the context of cognitive challenges like dementia or mood conditions like depression.See study design
What are the potential side effects?
Since this trial involves using a decision-making tool rather than medication, traditional physical side effects are not expected. However, participants may experience emotional or psychological responses.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
My medical records show I have early dementia or depression.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~assessed at 4 weeks post enrollment
This trial's timeline: 3 weeks for screening, Varies for treatment, and assessed at 4 weeks post enrollment for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Firearm storage (adapted from the National Firearm Survey)
Secondary outcome measures
Acceptability of Intervention Measure
Feasibility of intervention delivery
Knowledge Questionnaire
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Intervention ArmExperimental Treatment1 Intervention
Participants in this arm will receive the intervention and undergo research assessments.

Find a Location

Who is running the clinical trial?

University of WashingtonLead Sponsor
1,744 Previous Clinical Trials
1,848,311 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,682 Previous Clinical Trials
28,026,120 Total Patients Enrolled
Elizabeth PhelanPrincipal InvestigatorUniversity of Washington

Frequently Asked Questions

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

Are there any available openings for patients to participate in this study?

"Affirmative. The information available on clinicaltrials.gov indicates that this research study is currently seeking participants. Originally listed on April 1st, 2024, the trial was last modified on April 19th, 2024. There are openings for enrollment of up to 66 subjects at a single site."

Answered by AI

What is the total number of subjects actively involved in this research investigation?

"Indeed, data available on clinicaltrials.gov indicates that this particular trial is actively seeking participants. The study was initially posted on April 1st, 2024 and last revised on April 19th, 2024. A total of 66 individuals will be enrolled from one designated site."

Answered by AI
~33 spots leftby Jun 2024