The HARP study aims to observe the long-term clinical course of anxiety disorders and assess how comorbid psychiatric conditions influence recovery or recurrence. Participants were recruited and underwent baseline assessments in 1989 to 1991 after being referred from 11 clinical treatment facilities across the New England area of the United States of America. At baseline, there were 711 participants aged 18 to 86. Follow-up interviews were conducted at 6-month intervals for the first two years, annually for years 3-6, and then every 6 months from years 7 to 12. An associated study, Harvard/Brown Anxiety Research Project - Phase II (HARP-II), has similar aims but has recruited a new cohort of African American, Latino, and Non-Latino White participants.
Study design
Cohort - clinical
Number of participants at first data collection
711 (participants)
Age at first data collection
Varied (participants)
Participant year of birth
Varied (participants)
Participant sex
All
Representative sample at baseline?
No
Sample features
Country
Year of first data collection
1989
Primary Institutions
Brown University (Academic, United States of America)
Profile paper DOI
Funders
Eli Lilly and Company (Industry, United States of America)
National Institute of Mental Health (NIMH) (Government, United States of America)
Upjohn Company (Industry, United States of America)
Wyeth-Ayerst Laboratories (Industry, United States of America)
Ongoing?
Yes
Data types collected

Engagement
Keywords
Consortia and dataset groups