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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Exclusion criteria from MDS include active psychiatric diagnoses (bipolar disorder, major depressive episode, schizophrenia or schizoaffective disorder, mood disorder with psychotic features, psychotic symptoms, hallucinations or delusions); terminal illness (on hospice); and lack of verbal or non-verbal response to staff (MDS section B)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre (1 year), post (1 year)
Awards & highlights
No Placebo-Only Group
Summary
This trial will test a new online training program for nursing home staff to see if it improves communication and reduces behavioral symptoms in people with dementia.
Who is the study for?
This trial is for nursing homes with internet access, willing to have staff complete CHATO training and participate in interviews/surveys. It's aimed at improving care for residents with Alzheimer's or other dementias. Staff providing direct care for 8+ hours weekly will do the training. Facilities that served in prior CHAT/CHATO studies, assisted living, or those with residents on hospice or certain psychiatric conditions are excluded.
What is being tested?
The study tests an online interactive training program (CHATO) designed to enhance communication skills of nursing home staff. The goal is to improve interactions with dementia patients and reduce their behavioral symptoms, contributing to better overall care.
What are the potential side effects?
Since this intervention involves educational training without medical procedures or drugs, there are no traditional side effects. However, participants may experience changes in workload or stress levels due to new practices implemented from the training.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not have severe mental health issues, am not in hospice care, and can communicate with staff.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre (1 year), post (1 year)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre (1 year), post (1 year)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
AIM 1. Test CHATO's effects on Behavioral and Psychological Symptoms of Dementia (BPSD) - Change in MDS E0200 at 3 and 6 months
AIM 1. Test CHATO's effects on Behavioral and Psychological Symptoms of Dementia (BPSD) - Change in MDS E0800 at 3 and 6 months
AIM 1. Test CHATO's effects on Behavioral and Psychological Symptoms of Dementia (BPSD) - Change in MDS E1100 at 3 and 6 months
+6 moreSecondary study objectives
AIM 3. Evaluate CHATO Cost (3 months of training)
Aim 3. Evaluate CHATO Sustainability (1 year post-training)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
Intervention nursing homes will receive the training and control nursing homes will complete assessments, but not receive the training.
Group II: Waitlist ControlActive Control1 Intervention
After the intervention nursing homes complete the training, the waitlist control nursing homes will crossover and complete the training.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Changing Talk Online (CHATO)
2019
N/A
~220
Find a Location
Who is running the clinical trial?
University of IowaOTHER
468 Previous Clinical Trials
891,691 Total Patients Enrolled
University of Kansas Medical CenterLead Sponsor
510 Previous Clinical Trials
175,099 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- My facility provides care for individuals with dementia.My nursing home has internet for staff to do CHATO training.I am a permanent employee at a participating nursing home and work at least 8 hours a week providing direct care.I do not have severe mental health issues, am not in hospice care, and can communicate with staff.
Research Study Groups:
This trial has the following groups:- Group 1: Waitlist Control
- Group 2: Intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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