Los Angeles, CANCT06418971Now EnrollingIRB Ready

Caregiver Burden Clinical Trial in Los Angeles, CA

Access cutting-edge caregiver burden treatment through this clinical trial at a research site in Los Angeles. Study-provided care at no cost to qualified participants.

Sponsored by University of Southern California

Quick Self-Assessment

See if you qualify for this Los Angeles location

Preparing your pre-screening questions…

Expert Care in Los Angeles

Access caregiver burden specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related caregiver burden treatment provided free

Apply for This Los Angeles Location

Check if you qualify for this caregiver burden clinical trial in Los Angeles, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Los Angeles

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Los Angeles site if eligible
  4. 4Begin participation

About This Caregiver Burden Study in Los Angeles

The purpose of this study is to develop and test CarePair, a mobile application-based needs assessment and service referral platform for family caregivers of persons with dementia designed to alleviate stress and promote psychosocial well being. The main aims of this study are: * To evaluate the feasibility and acceptability of the CarePair mobile application. * To explore the potential for CarePair to reduce feelings of depression and burden, and improve caregivers' feelings of self-efficacy. Caregiver participants will be asked to log in and use the CarePair application and complete study activities for a six-week duration. Researchers will compare the intervention group to an attention control comparator to see if application use is associated with improved psychosocial outcomes at follow-up.

Sponsor: University of Southern California

Who Can Participate

Inclusion Criteria

Currently a primary caregiver of a community-dwelling PwD
Provides at least 10 hours of care per week
≥18 years of age
Fluent in English
Both the caregiver and care-recipient reside in and/or can easily access one of the following cities/areas: New York City, New York (NY); Long Island, NY; Westchester County, NY; Seattle, Washington (WA); Los Angeles, California (CA)
Provides at least 10 hours of care per week
Has provided care for at least 6 months
Able to use the internet and has internet access
Owns and can operate a smartphone
Able and willing to provide their informed consent to participate for the six-week study duration
Does not self-report any cognitive impairments

Exclusion Criteria

Not currently the primary caregiver of a community-dwelling person with dementia
Care-recipient lives in residential care (e.g., assisted living, skilled nursing facility)
≤18 years of age
Not fluent in English
The caregiver and/or care-recipient resides outside of and/or cannot easily access any of the following cities: New York City (NY); Long Island (NY); Westchester County (NY); Seattle (WA); Los Angeles (CA)
Provides less than 10 hours of care per week
Has provided care for less than 6 months
Unable to use the internet or does not have internet access
Does not own and/or cannot operate a smartphone
Unable or unwilling to provide informed consent to participate for the six-week study duration
Self-reports having a cognitive impairment

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Los Angeles?

Yes, this clinical trial (NCT06418971) has an active research site in Los Angeles, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Caregiver Burden Treatment Options in Los Angeles, CA

If you're searching for caregiver burden treatment options in Los Angeles, CA, this clinical trial (NCT06418971) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Los Angeles research site is actively enrolling participants for this clinical trial. You'll receive care from experienced caregiver burden specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Ready to Join in Los Angeles?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Los Angeles, CA