Writing Intervention for Cognitive Health in Older Adults
What You Need to Know Before You Apply
What is the purpose of this trial?
UCLA researchers looking for healthy older adults (aged 65+) to participate in a study investigating how writing about experiences can affect your brain and body.Once a week for 6 weeks, participants will write about their experiences and fill out online questionnaires. Participants will also come to the UCLA campus to complete a neuroimaging session (fMRI), provide a blood spot sample, and fill out questionnaires 2 times: once prior to the 6-week writing period and once immediately after the 6-week writing period.
Do I need to stop taking my current medications for the trial?
The trial excludes participants using certain medications like steroids and opioids. If you are taking these, you may need to stop, but the protocol does not specify a washout period.
Is writing therapy safe for humans?
How is the Writing Intervention treatment different from other treatments for cognitive health in older adults?
Writing Intervention, such as Expressive Writing Therapy, is unique because it uses writing as a form of emotional expression to improve cognitive and emotional health, unlike traditional treatments that may not focus on personal storytelling and emotional disclosure. This approach can be done individually or in groups, providing flexibility and a non-pharmacological option for enhancing mental well-being.26789
What data supports the effectiveness of the treatment Writing Intervention, Expressive Writing Therapy, Narrative Exposure Therapy, Therapeutic Writing for cognitive health in older adults?
Research shows that writing therapy, including expressive writing, can help improve mood and reduce symptoms of depression and distress. It has been used effectively in various therapies to promote psychological well-being and personal growth, suggesting potential benefits for cognitive health in older adults.348910
Are You a Good Fit for This Trial?
Healthy adults aged 65 and older can join this UCLA study. It's not for those with chronic infections like Hepatitis C or HIV, a BMI over 35, claustrophobia, current smokers, uncontrolled medical issues, major psychiatric conditions, left-handedness, body metal implants or on steroids/opioids.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants write about their experiences and fill out online questionnaires once a week for 6 weeks. They also complete a neuroimaging session (fMRI), provide a blood spot sample, and fill out questionnaires at the start and end of the 6-week period.
Follow-up
Participants are monitored for changes in inflammatory gene expression, social support, social participation, and psychological distress.
What Are the Treatments Tested in This Trial?
Interventions
- Writing Intervention
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of California, Los Angeles
Lead Sponsor