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Clinical Trials/NCT05738122
NCT05738122CompletedNot Applicable

Evaluating the Efficacy of a 60-day Self-guided Emotion Regulation Journal

University of Victoria2 sites in 1 country30 target enrollmentStarted: January 18, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
2
Primary Endpoint
Participant Emotion Regulation

Study Overview

Brief Summary

Participants randomized to the intervention group will receive a physical copy of the 60-day emotion regulation journal during the baseline meeting. Participants will also be introduced the purpose of the journal and its intended usage (i.e., daily journaling). Intervention participants will not be offered guidance or feedback on the journal after these initial instructions, in order to emulate an ad libitum usage. Control group participants will not receive any contact with the researchers outside of the planned questionnaires and to receive their journal at the two-month timepoint.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • (1) being 18+ years old (2) being fluent in English, (3) currently living in the Greater Victoria area, (4) self-reporting no previously diagnosed mental illness or psychiatric conditions, and (5) scoring a mean of <4.6 on the Cognitive Reappraisal, and mean of >3.14 on the Expressive Suppression subscales of the Emotion Regulation Questionnaire (based on previous mean data)

Exclusion Criteria

  • Scoring a mean of ≥4.6 on the Cognitive Reappraisal or a mean of ≤3.14 on the Expressive Suppression subscales of the Emotion Regulation Questionnaire, currently receiving or seeking therapy for a mental illness, a current or previous diagnosis of mental illness, or self-identifying as neurodivergent.

Outcomes

Primary Outcomes

Participant Emotion Regulation

Time Frame: 2 weeks, 1-month, 2-months, 60 day exit interview, 90 days follow up

Change in participants' emotion regulation abilities and habits assessed using the Emotion Regulation Questionnaire.

Secondary Outcomes

  • Adherence(2 weeks, 1-month, 2-months)
  • Mental Health(2 weeks, 1-month, 2-months, and 3-month follow up for intervention group)
  • Subjective Well-Being(2 weeks, 1-month, 2-months, and 3-month follow up for intervention group)
  • Self-Compassion(2 weeks, 1-month, 2-months, and 3-month follow up for intervention group)
  • Physical Activity and Sedentary Behaviour(2 weeks, 1-month, 2-month, and 3-month follow up for intervention group)
  • Screen Time(2 weeks, 1-month, 2-month, and 3-month follow up for intervention group)
  • Sleep(2 weeks, 1-month, 2-month, and 3-month follow up for intervention group)
  • Experience using journal(60 days)
  • Demographics(Baseline)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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