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Control Group for Dementia
N/A
Waitlist Available
Led By Nicole McClure, MS, MA
Research Sponsored by University of Central Florida
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
The Three Good Things (3GT) is a gratitude list intervention that is empirically supported (Emmons \& McCullough, 2003; Seligman et al., 2005) and is a low-cost, easily accessible tool for medical and mental providers to recommend and dementia caregivers to implement independently. Thus, this study aims to investigate the feasibility of use of 3GT in the dementia caregiving population and investigate potential therapeutic mechanisms of the intervention.
Eligible Conditions
- Dementia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Assess caregiver burden using the Zarit Burden Interview
To asses ICN1-10 validity, the Burnout Measure, Short (BMS) will be used
To assess positive emotion using The Positive and Negative Affect Schedule (PANAS)
+6 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Active Control
Group I: Control GroupActive Control1 Intervention
Participants will be asked to reflect on early memories of their life, with no specific prompts provided, for 15 days during the evening. This activity is consistent with prior efficacy studies of 3GT (Seligman et al., 2005).
Group II: Intervention Protocol (The 3GT)Active Control1 Intervention
Participants will be asked to identify three things that went well that day and their role for this occurring \["What went well today, and what was your role in making it happen?" as adapted from (Sexton \& Adair, 2019)\]. They will be asked to engage in this exercise for 15 days during the evening.
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Who is running the clinical trial?
University of Central FloridaLead Sponsor
91 Previous Clinical Trials
1,120,135 Total Patients Enrolled
2 Trials studying Dementia
80 Patients Enrolled for Dementia
Nicole McClure, MS, MAPrincipal InvestigatorUniversity of Central Florida
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