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Therapy for Caregiver Depression (CARES Trial)

N/A
Recruiting
Led By Stephen F Smagula, PhD
Research Sponsored by University of Pittsburgh
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
No or stable pharmacotherapy for depression
Age 60 years or older
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, continuously up to weekly for 6-weeks, and follow-up (6 months)
Awards & highlights

CARES Trial Summary

This trial will test two different types of therapy to see which is more effective in treating depression.

Who is the study for?
This study is for individuals aged 60 or older who are unpaid caregivers to someone with dementia, feeling stressed, and have trouble getting going in the morning. They shouldn't be currently receiving cognitive therapy, have a substance use disorder, probable dementia themselves, or any condition that prevents MRI scans.Check my eligibility
What is being tested?
The trial tests whether certain interventions like adjusting sleep-wake times and morning routines can help reduce depression symptoms and improve brain function related to mood in caregivers experiencing stress.See study design
What are the potential side effects?
Since this trial involves behavioral strategies rather than medications, side effects may include emotional discomfort or fatigue due to changes in routine but are not expected to involve physical health risks.

CARES Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
My depression medication has not changed recently.
Select...
I am 60 years old or older.

CARES Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, continuously up to weekly for 6-weeks, and follow-up (6 months)
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, continuously up to weekly for 6-weeks, and follow-up (6 months) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change from baseline in anxiety symptoms at 6-months
Change from baseline in depressive symptoms at 6-months
Change from baseline in rumination at 6-months
+4 more
Secondary outcome measures
Change in cognitive functioning at 6-weeks
Change in executive function at 6-weeks
Change in morning light exposure at 6-weeks
+3 more

CARES Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Active condition (SAMM Protocol)Experimental Treatment3 Interventions
The goal of the SAMM protocol is to increase morning activity engagement over a 6-week period. Participants in this condition will review their morning routine, and make a list of potential morning activities to add. They will choose one activity and develop a plan for doing it. Each day, participants are asked to track if they do the morning activity plan. If unsuccessful, at weekly follow-ups, participants are asked to refine their plan or make a new one.
Group II: Attention-matched supportive control conditionActive Control1 Intervention
Participants in this condition will receive sessions in the same number and duration as the SAMM experimental condition. Therapists will create a comfortable environment by demonstrating interest, empathy, and acceptance without judgment. Caregivers will be encouraged to talk about stressors they experience, providing an opportunity to voice and self-address their problems. In this control condition, therapists will not deliver any particular strategy except for active listening and referring to the educational materials.

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
Behavioral therapies, such as cognitive-behavioral therapy (CBT) and mindfulness-based cognitive therapy (MBCT), are common treatments for Caregiver Burden. These therapies work by helping individuals identify and change negative thought patterns and behaviors, and by incorporating mindfulness strategies to focus on the present moment and reduce stress. These mechanisms are crucial for caregivers as they can significantly reduce psychological distress, improve coping strategies, and enhance overall well-being, addressing the high levels of stress and emotional burden that caregivers often face.
A pilot randomized controlled trial of E-care for caregivers: An internet intervention for caregivers of depressed patients.

Find a Location

Who is running the clinical trial?

University of PittsburghLead Sponsor
1,732 Previous Clinical Trials
16,307,052 Total Patients Enrolled
1 Trials studying Caregiver Burden
150 Patients Enrolled for Caregiver Burden
National Institute of Mental Health (NIMH)NIH
2,807 Previous Clinical Trials
2,665,546 Total Patients Enrolled
Stephen F Smagula, PhDPrincipal InvestigatorUniversity of Pittsburgh

Media Library

Activity Strategy-based Session with Therapist Clinical Trial Eligibility Overview. Trial Name: NCT05219955 — N/A
Caregiver Burden Research Study Groups: Active condition (SAMM Protocol), Attention-matched supportive control condition
Caregiver Burden Clinical Trial 2023: Activity Strategy-based Session with Therapist Highlights & Side Effects. Trial Name: NCT05219955 — N/A
Activity Strategy-based Session with Therapist 2023 Treatment Timeline for Medical Study. Trial Name: NCT05219955 — N/A
~60 spots leftby Jun 2026