- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03669016
MIndfulness for Students (Mindfulstud)
Mindfulness for Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The hypotheses is that participating to the mindfulness intervention improves students well-being and decreases their level of stress. These are measured by self-evaluation questionnaires and with hair samples, before the intervention, immediately after intervention and four months after the intervention.
This is a randomized control trial. There are two different experiment groups and one waiting-list control group. The target group is all undergraduate students in the Faculty of Medicine, University of Helsinki. The participants are recruited with e-mail and informing students in different situations. The aimed amount of participants is 120-150 but the study will be conducted if 90 participants are recruited. The participants enroll to the study by signing consent format.
This is a follow-up research. The person register (name, university e-mail address, student number) are used to recruitment and to ensure the participants identity.
Time of data preservation is 10 years. The last student register data is going to be collected 2019. The data is preserved until age 2029.
The questionnaire with which the main data is been collected is Webropol questionnaire tool. The data is removed from the Webropol after three months of the end of the questionnaire answer time. The person responsible for the data removes the data from University's server after ten years.
Content of the register
- Mindfulness for Students questionnaire data
- Mindfulness for Students hair samples
- Mindfulness for students -observation log
- Mindfulness for students -interview data
- Data collected in Student Compass -internet environment
- Data of students' credits are collected from University's own credit register "Oodi", if participant has given a consent to that.
Students are being recruited in information meeting. They will be informed orally in that situation and given a written communication paper. The students who want to participate the course, will fill and sign a consent format. In format there is a research number code given to the student. The connection between the student identity and the research code number is known only by the persons that are responsible for the database.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Saara Repo, PhD
- Phone Number: +358405189456
- Email: saara.repo@helsinki.fi
Study Contact Backup
- Name: Tiina Paunio, PhD
- Phone Number: +358947163734
- Email: tiina.paunio@helsinki.fi
Study Locations
-
-
University Of Helsinki
-
Helsinki, University Of Helsinki, Finland, 00014
- Recruiting
- University of Helsinki
-
Contact:
- Saara Repo, PhD
- Phone Number: +358405189456
- Email: saara.repo@helsinki.fi
-
Contact:
- Tiina Paunio, PhD
- Phone Number: +358947163734
- Email: tiina.paunio@helsinki.fi
-
Principal Investigator:
- Saara Repo, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- All undergraduate students of Faculty of Medicine, University of Helsinki who have started their studies in year 2009 or after that.
Exclusion Criteria:
- The participants that can not participate fully to the intervention (self-evaluated).
- Participants who have severe mental problems (like anxiety or depression) when the study starts,
- Participants who have hade a great loss or trauma in near past, or some other mental or physical health problem that could make participation difficult.
This is evaluated based on how the participants answers to the base line questionnaire the following measures:
- answers to the CORE-OM questionnaire and
- answers to the questions where participants evaluate themselves their anxiety, depression, mental health.
- If participant tell they have some other mental disorder, they are not accepted to the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Face-to-face group-based mindfulness
8 weeks training.
|
An eight-week course, including 75-90 minutes once-a-week meeting.
Participants are supposed to practice mindfulness skills in their spare time 10-30 minutes per day.
An eight-week course, including 75-90 minutes once-a-week meeting.
Participants are supposed to practice mindfulness skills in their spare time 10-30 minutes per day.
This training is based on Jon Kabat-Zinn's course Mindfulness Based Stress Reduction and book Williams & Penman Mindfulness: a practical guide to finding peace in a frantic world and adapted for university students.
In addition, a manual written in Cambridge University "Mindfulness Skills for Students" is utilized.
|
Experimental: Internet-based mindfulness
8 weeks training.
|
An eight-week course, including 60 minutes starting and ending meeting.
Participants are practicing mindfulness, doing other tasks (writing, reading, reflecting) on their own.
This course is created in University of Jyväskylä, Finland.
It is based on mindfulness and Acceptance and Commmitment Therapy.
|
No Intervention: Waiting-list control group
No training during the study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Baseline CORE-OM measure at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
CORE-OM, Clinical Outcomes in Routine Evaluation Outcome Measure.
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Baseline rate of stress at post-intervention and 4-month follow-up.
Time Frame: It is measured in the same day when the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Cortisol as an indicator of stress which is measured from hair samples.
Stadler & Kirschbaum 2012.
|
It is measured in the same day when the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of resilience in studies at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Workplace Acceptance and Action Questionnaire (WAAQ) applied for students.
Bond, Joda, and Guenole 2013; Asikainen, Hailikari, Mattson 2017.
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of social support in studies at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Application of questionnaires of social support from Sarason et al. 1987 and Pyörälä et al. 2015.
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of study load in studies at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Application of questionnaire of healthy work measure of Karasek & Theorell 1990.
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Students' possibilities to influence to their own studies
Time Frame: It is measured three weeks before the interventions start.
|
Application of measures of healthy work measure.
Karasek & Theorell 1990.
|
It is measured three weeks before the interventions start.
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Change from Baseline rate of functional ability in studies at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Application of functional ability at work.
Tuomi et al. 1998.
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of subjective experience of quality of life at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Subjective experience of quality of life.
One Likert-scale question adapted and modified from three different questionnaires.
Koivumaa et al. 2000; Allardt 1973; Lundqvist & Mäkiopas 2016)
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Change from Baseline rate of mental well-being Scale at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
The Warwick-Edinburgh Mental Well-being Scale
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of Personality at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Parts of Big Five (Lang et al. 2011)
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Change from Baseline rate of sense of coherence at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Sence of coherence - SOC 3 (Antonovsky 1987; Schumann et al. 2003)
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It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Change from Baseline rate of Resilience at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Resilience scale (Wagnild & Young, 1993; Losoi et al 2013 modified)
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of experiences of own health at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Questionnaire Kunttu et al. 2017
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of quality and length of sleep at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Basic Nordic Sleep Questionnaire shortened (Partinen & Gislason 1995)
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of fatigue in day-time at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Questionnaire from Health 2000/2001 Research in Finland
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It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline amount of nightmares during previous month at post-intervention and 4-month follow-up.
Time Frame: IIt is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Application of questionnaire Sandman et al 2015.
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IIt is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Participant's own evaluation of his/her mental health
Time Frame: Three weeks before the intervention starts
|
Participant's own evaluation of the symptoms of mental health during previous month.
|
Three weeks before the intervention starts
|
Change from Baseline approximate amount of exercise at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Questionnaire from Health 2000/2001 Research in Finland
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Change from Baseline regularity of eating habits at post-intervention and 4-month follow-up.
Time Frame: It is measured before intervention, post-intervention and 4-month follow-up.
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Participant's own evaluation of the regularity of eating habits.
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It is measured before intervention, post-intervention and 4-month follow-up.
|
Change from Baseline approximate amount of caffeine used daily. at post-intervention and 4-month follow-up.
Time Frame: IIt is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Participant's own evaluation of the amount of daily caffeine use.
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IIt is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Change from Baseline approximate amount use of alcohol and cigarettes daily.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Participant's own evaluation of approximate amount use of alcohol and cigarettes daily.
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It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Change from Baseline rate of Mindfulness skills at post-intervention and 4-month follow-up.
Time Frame: It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Freiburg Mindfulness Index (FMI) Walach, H., Buchheld, N., Buttenmüller, V., Kleinknecht, N., & Schmidt, S. 2006; Lehto, Uusitalo-Malmivaara & Repo 2015.
|
It is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Change from Baseline rate of stress and recovery of it at post-intervention and 4-month follow-up.
Time Frame: IIt is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Application of measures of healthy work measure of Lundqvist & Mäkiopas 2016 and Elo et al. 1992.
|
IIt is measured three weeks before the intervention starts, immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Previous experience in practicing of mindfulness and/or meditation
Time Frame: It is measured three weeks before the intervention starts.
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Participant's own evaluation of the amount of previous experience in practicing mindfulness and/or meditation
|
It is measured three weeks before the intervention starts.
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Amount and quality of independent mindfulness practice
Time Frame: Immediately after the 8-week intervention is finished.
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Participant's self-evaluation of amount and quality of independent mindfulness practice
|
Immediately after the 8-week intervention is finished.
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Change from post-intervention amount and quality of independent mindfulness practice at 4-month follow-up.
Time Frame: Immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
|
Participant's self-evaluation of amount and quality of independent mindfulness practice.
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Immediately after the 8-week intervention is finished, and 4-month after the intervention is finished.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Saara Repo, PhD, University of Helsinki
Publications and helpful links
General Publications
- Kunzler AM, Helmreich I, Konig J, Chmitorz A, Wessa M, Binder H, Lieb K. Psychological interventions to foster resilience in healthcare students. Cochrane Database Syst Rev. 2020 Jul 20;7(7):CD013684. doi: 10.1002/14651858.CD013684.
- Daya Z, Hearn JH. Mindfulness interventions in medical education: A systematic review of their impact on medical student stress, depression, fatigue and burnout. Med Teach. 2018 Feb;40(2):146-153. doi: 10.1080/0142159X.2017.1394999. Epub 2017 Nov 7.
- Miller R, Wankerl M, Stalder T, Kirschbaum C, Alexander N. The serotonin transporter gene-linked polymorphic region (5-HTTLPR) and cortisol stress reactivity: a meta-analysis. Mol Psychiatry. 2013 Sep;18(9):1018-24. doi: 10.1038/mp.2012.124. Epub 2012 Sep 4.
- Galante J, Dufour G, Vainre M, Wagner AP, Stochl J, Benton A, Lathia N, Howarth E, Jones PB. A mindfulness-based intervention to increase resilience to stress in university students (the Mindful Student Study): a pragmatic randomised controlled trial. Lancet Public Health. 2018 Feb;3(2):e72-e81. doi: 10.1016/S2468-2667(17)30231-1. Epub 2017 Dec 19.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MIndfulness for Students
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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