Comparing Targets of Expressive Writing
1 other identifier
interventional
160
1 country
1
Brief Summary
Expressive writing involves writing about one's deepest thoughts and feelings surrounding an emotional event. The current literature on the efficacy of expressive writing is mixed and warrants further investigation into how, when, and for whom expressive writing is an effective intervention. The goal of this study is to compare the efficacy of expressive writing interventions in young adults when people imagine that they're writing to themselves vs. a loved one. Participants will carry out an expressive writing exercise for 14 consecutive days. Participants are randomized into 3 groups: Self, Other, and Control. The Self group is instructed to write as if they were talking to themselves. The Other group is instructed to direct their writing to someone they feel close to. The Control group is asked to write down a factual description of their routine that day, and direct this writing to themselves. We will recruit participants until we have usable data from 53 participants per group (i.e., 159 in total).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable healthy
Started Nov 2023
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 6, 2023
CompletedStudy Start
First participant enrolled
November 10, 2023
CompletedFirst Posted
Study publicly available on registry
November 13, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2025
CompletedFebruary 23, 2026
February 1, 2026
2 years
November 6, 2023
February 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Anxiety
Generalized Anxiety Disorder-7 (GAD-7). Scores range from 0-21, with higher scores indicating more severe anxiety.
Initial visit (day 1), mid-point (day 7) final visit (day 15), 1-month follow-up (1 month after day 14)
Depression
Patient Health Questionnaire-8 (PHQ-8). Scores range from 0-24, with higher scores indicating more severe depression.
Initial visit (day 1), mid-point (day 7), final visit (day 15), 1-month follow-up (1 month after day 14)
Other Outcomes (10)
Sleep Quality
Initial visit (day 1), final visit (day 15), 1-month follow-up (1 month after day 14)
Depression, Anxiety, and Stress
Initial visit (day 1), final visit (day 15), 1-month follow-up (1 month after day 14)
Alexithymia (TAS)
Initial visit (day 1), final visit (day 15), 1-month follow-up (1 month after day 14)
- +7 more other outcomes
Study Arms (3)
Self
EXPERIMENTALThe Self group is instructed to carry out the expressive writing exercise as if they were writing to themselves.
Other
EXPERIMENTALThe Other group is instructed to carry out the expressive writing exercise as if they were writing to someone they feel close to.
Control
PLACEBO COMPARATORThe Control group is asked to write down a factual description of their routine that day, as if they were writing to themselves.
Interventions
This intervention consists of a daily expressive writing exercise carried out for 14 consecutive days, for 15 minutes each day. Expressive writing involves asking participants to write about their deepest thoughts and feelings surrounding an emotional event. Participants in this condition will write as if they are writing to themselves.
This intervention consists of a daily expressive writing exercise carried out for 14 consecutive days, for 15 minutes each day. Expressive writing involves asking participants to write about their deepest thoughts and feelings surrounding an emotional event. Participants in this condition will write as if they are writing/talking to someone they're close to.
This intervention consists of a daily factual writing exercise carried out for 14 consecutive days, for 15 minutes each day. Participants are asked to give a factual description of their day. This is a standard control for Expressive writing studies. Participants in this condition will be asked to direct their writing to themselves.
Eligibility Criteria
You may qualify if:
- US-based
- Fluent English
- Combined GAD-7 and PHQ-8 score of ≥ 5
You may not qualify if:
- "Completion" of a writing session requires participants to spend at least 15 minutes on the writing page. We will monitor completion of the daily writing exercise, and will contact participants who miss or spend less than 15 minutes on the exercise. Participants who fail to complete 3 consecutive daily writing sessions will be deemed non-compliant, removed from the study, and paid a prorated amount for the tasks they have completed in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peretsman Scully Hall
Princeton, New Jersey, 08540, United States
Related Publications (1)
Pennebaker JW, Beall SK. Confronting a traumatic event: toward an understanding of inhibition and disease. J Abnorm Psychol. 1986 Aug;95(3):274-81. doi: 10.1037//0021-843x.95.3.274. No abstract available.
PMID: 3745650BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Erik Nook, PhD
Princeton University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 6, 2023
First Posted
November 13, 2023
Study Start
November 10, 2023
Primary Completion
October 30, 2025
Study Completion
October 30, 2025
Last Updated
February 23, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP, ANALYTIC CODE
- Time Frame
- Beginning after publication of results with no end date.
- Access Criteria
- A subset of the de-identified data will be publicly available on the OSF.
Upon study completion, a subset of the de-identified data will be transferred to OSF, which will provide public access to this data. Writing content will not be transferred to OSF, though we will make thoroughly de-identified data available to researchers who have completed appropriate ethics training, agree to confidentiality restrictions, and whose research goals are in line with the purpose of this study.