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Caregiver Coaching for Dementia (CuRB-IT Trial)
N/A
Recruiting
Led By Rita A Jablonski, PhD
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
The care provided consists of help with at least 2 Instrumental Activities of Daily Living or one Activity of Daily Living
Be older than 18 years old
Must not have
Persons who cannot speak/read English
Timeline
Screening 3 weeks
Treatment Varies
Follow Up daily during weeks 49, 50, and 51
Awards & highlights
No Placebo-Only Group
Summary
This trial tests an online training program called CuRB-IT, which helps family caregivers of people with dementia manage difficult behaviors. The program aims to boost caregivers' confidence and provide practical coping methods, making caregiving less stressful.
Who is the study for?
This trial is for family caregivers over 18 years old who help a relative with mild cognitive impairment or dementia and face resistance when providing care. Caregivers must speak/read English, have internet access, and share living or cooking space with the care recipient.
What is being tested?
The study tests CuRB-IT, an intervention for caregivers dealing with care-resistant behavior in dementia patients. Participants are split into two groups: one starts CuRB-IT immediately and the other after a delay, both completing surveys and diaries to track progress.
What are the potential side effects?
Since this trial involves coaching rather than medication, there aren't typical drug side effects. However, participants may experience emotional distress or fatigue from discussing caregiving challenges.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I need help with daily tasks like dressing or using the bathroom.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot speak or read English.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ daily during weeks 49, 50, and 51
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~daily during weeks 49, 50, and 51
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Dementia
Change in caregiver self-efficacy coping skills
Change in caregiver self-efficacy measured by selection of items from 10-item CurB-CuRB-IT Strategy checklist
+1 moreAwards & 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: Immediate InterventionExperimental Treatment1 Intervention
Complete baseline survey, complete 3 weeks of daily diaries and intermittent survey, receive 12 weeks of CurB-IT, then complete 3 rounds of 21-day daily diaries and intermittent surveys while receiving attention during the 12-week intervals between daily diaries.
Group II: Delayed interventionActive Control1 Intervention
Complete baseline survey, complete 3 weeks of daily diaries, receive 12 weeks of attention, complete 3 weeks of daily diaries and 1 intermittent survey, receive 12 weeks of CurB-IT, then complete 2 rounds of 21-day daily diaries and intermittent surveys while receiving attention during the 12-week intervals between daily diaries.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for dementia include pharmacologic approaches like cholinesterase inhibitors (e.g., donepezil) and NMDA receptor antagonists (e.g., memantine), which work by enhancing neurotransmitter function and slowing cognitive decline. Nonpharmacologic treatments, such as caregiver support programs like CuRB-IT, focus on reducing caregiver stress and enhancing coping strategies.
These interventions are crucial as they improve the caregiving environment, potentially leading to better patient outcomes and reduced caregiver burnout.
Enhanced rehabilitation and care models for adults with dementia following hip fracture surgery.Recruiting Dementia Caregivers Into Clinical Trials: Lessons Learnt From the Australian TRANSCENDENT Trial.
Enhanced rehabilitation and care models for adults with dementia following hip fracture surgery.Recruiting Dementia Caregivers Into Clinical Trials: Lessons Learnt From the Australian TRANSCENDENT Trial.
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Who is running the clinical trial?
University of Alabama at BirminghamLead Sponsor
1,645 Previous Clinical Trials
2,342,586 Total Patients Enrolled
12 Trials studying Dementia
807 Patients Enrolled for Dementia
Rita A Jablonski, PhDPrincipal InvestigatorUniversity of Alabama at Birmingham
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I cannot speak or read English.I am over 18, care for a family member aged 60+ without pay, and we live together or share a kitchen.I refuse or struggle to accept help with daily tasks.I need help with daily tasks like dressing or using the bathroom.
Research Study Groups:
This trial has the following groups:- Group 1: Immediate Intervention
- Group 2: Delayed 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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