ClinicalTrials.Veeva

Menu

Neural and Physiological Responses to Real-World Experiences

University of California, Los Angeles (UCLA) logo

University of California, Los Angeles (UCLA)

Status

Completed

Conditions

Gene Expression

Treatments

Other: Writing about places, objects
Behavioral: Writing about people

Study type

Interventional

Funder types

Other

Identifiers

NCT01723410
GGSC-GRAT

Details and patient eligibility

About

UCLA researchers looking for healthy individuals (aged 35-50) who have a home computer with internet access, are not pregnant, planning to become pregnant, or currently breastfeeding (if female), to participate in a study investigating whether real-world experiences alter the brain and body. This study takes place over an eight week period and involves providing the names of 8 close friends or family members, completing a neuroimaging session, providing blood and saliva (for genetic analysis), and a 6-week period in which participants login twice a week to complete online questionnaires. Compensation is up to $210 for those who complete all aspects of the study. Please email realworld.ucla@gmail.com for more information.

Enrollment

70 patients

Sex

All

Ages

35 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults between the ages of 35-50

Exclusion criteria

Following a structured telephone interview, prospective participants with the following conditions will not be able to participate:

  1. claustrophobia, left-handedness, or presence of metal in their body (for the neuroimaging procedures),
  2. possible presence of a depressive disorder, which may interfere with the gratitude intervention (assessed by the Patient Health Questionnaire; Spitzer et al., 1999),
  3. regular use of medications that may impact inflammatory processes (anti-inflammatory drugs, steroids, opioids),
  4. current smokers or excessive caffeine users (> 600 mg/day) because of known effects on inflammation, and
  5. pregnancy (which would affect oxytocin gene expression).

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups, including a placebo group

Writing condition
Experimental group
Description:
Subjects will be asked to write about other individuals in their lives.
Treatment:
Behavioral: Writing about people
Writing
Placebo Comparator group
Description:
Subjects will be asked to write about places or objects in their lives.
Treatment:
Other: Writing about places, objects

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems