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Completed

NCT Number: NCT05738122

Evaluating the Efficacy of a 60-day Emotion Regulation Journal

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.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Behavioural Medicine Lab - University of Victoria

Victoria, British Columbia, V8P 5C2, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

60-Day self-guided Emotion Regulation Journal

Other

A 60-day self guided journal with activities designed to be completed daily to improve an individual's emotion regulation abilities and habits

Primary outcomes

  1. 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.

  2. 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 using the Difficulties in Emotional Regulation.

Secondary outcomes

  1. Adherence

    Time frame: 2 weeks, 1-month, 2-months

    Participants' adherence to the 60-days of activities in the journal assessed using three items: "Currently, what is the last day of the journal you have completed?"; "Have you skipped or not completed any days prior to the latest day you have completed?"; and "Approximately how many minutes do you spend completing a day, within the journal?"

  2. Experience using journal

    Time frame: 60 days

    Usability and user experience of intervention group collected during exit interview

  3. Demographics

    Time frame: Baseline

    Age, preferred gender, socio-economic status, ethnicity, educational attainment, and employment status will be collected.

  4. Mental Health

    Time frame: 2 weeks, 1-month, 2-months, and 3-month follow up for intervention group

    Depression and anxiety will be assessed using the Hospital Anxiety and Depression Scale. There is a minimum score of 0 and a maximum score of 21 for each anxiety and depression. Individuals with a score of greater than 8 are considered to have considerable symptoms of anxiety and/or depression.

  5. Subjective Well-Being

    Time frame: 2 weeks, 1-month, 2-months, and 3-month follow up for intervention group

    Subjective well-being will be assessed using the Warwick-Edinburgh Mental Wellbeing Scale. There is a minimum score of 14 and a maximum score of 70. Scores above 51 are above mean population mental well-being while a score below 51 is below mean population mental well-being.

  6. Self-Compassion

    Time frame: 2 weeks, 1-month, 2-months, and 3-month follow up for intervention group

    Self-Compassion will be assessed using the full version of the Self-Compassion Scale. Minimum score is 1 and Maximum score is 5. Scores from 1-2.5 indicate low self-compassion, 2.5-3.5 indicates moderate, and 3.5-5 indicates high self-compassion.

  7. Physical Activity and Sedentary Behaviour

    Time frame: 2 weeks, 1-month, 2-month, and 3-month follow up for intervention group

    Past week hours of sitting, walking, mild, moderate, and vigorous physical activity will be assessed using a modified version of the International Physical Activity Questionnaire. A HIGH score consists of vigorous intensity activity on at least 3 days OR 7 or more days of any combination of walking, moderate intensity or vigorous intensity activities. A MODERATE score consists of 3 or more days of vigorous intensity activity and/or walking of at least 30 minutes per day OR 5 or more days of moderate intensity activity and/or walking of at least 30 minutes per day OR 5 or more days of any combination of walking, moderate intensity or vigorous intensity activities. A LOW score is not achieving the high or moderate physical activity levels.

  8. Screen Time

    Time frame: 2 weeks, 1-month, 2-month, and 3-month follow up for intervention group

    Past week average weekday and weekend occupational and recreational (i.e., leisure) screen time hours will be assessed using four bespoke items (e.g., In the last seven days, on an average weekday, how many hours did you spend using screens for recreational purposes (e.g., watching TV, playing video games)?)

  9. Sleep

    Time frame: 2 weeks, 1-month, 2-month, and 3-month follow up for intervention group

    Past week average hours of sleep will be assessed using an adapted item from the Pittsburgh Sleep Quality Assessment: 20 "During the past week, how many hours of actual sleep did you get at night?". The minimum score is 0 representing 7 or more hours of sleep and the maximum score is 3 representing less than 5 hours of sleep. The higher the score, the worse the sleep duration.

Sponsors and collaborators

Lead sponsor

University of Victoria

Other

Collaborators

  • Mathematics of Information Technology and Complex Systems
  • Switch Research

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Feb 21, 2023
Registry last updated
Apr 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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