Mindful Self-compassion and Perfectionism
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| ClinicalTrials.gov Identifier: NCT03453437 |
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Recruitment Status :
Completed
First Posted : March 5, 2018
Last Update Posted : August 17, 2021
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Perfectionism Depression Anxiety Body Image | Behavioral: Mindful Self-Compassion | Not Applicable |
The investigators will test four hypotheses:
- At baseline, low levels of maladaptive perfectionism, and lower levels of depression, anxiety and body appreciation - reversed, will be related to greater self-compassion. The investigators expect high level of maladaptive perfectionism to be related to lower baseline self-compassion, higher levels of depression and anxiety and lower levels of body appreciation.
- The intervention, a five session self-compassion intervention, will be sufficient to induce positive changes in perfectionism and psychological symptoms of anxiety, depression and body-appreciation- reversed.
- Changes in self-compassion will co-vary with changes in maladaptive perfectionism and body appreciation.
- Higher baseline levels of maladaptive perfectionism will predict greater gains from the intervention, because perfectionistic students will have greater need for a self-compassion intervention.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 379 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | A Randomized Controlled Trial of a Mindful Self-compassion Intervention to Improve Evaluative Concerns Perfectionism, Depression, Anxiety, and Unhealthy Body Image in College Students |
| Actual Study Start Date : | February 3, 2018 |
| Actual Primary Completion Date : | May 14, 2019 |
| Actual Study Completion Date : | May 14, 2019 |
| Arm | Intervention/treatment |
|---|---|
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No Intervention: Control group
Receiving no intervention (control groups will be offered the intervention after the experimental group has completed the course)
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Experimental: Active group
Receiving Mindful Self-Compassion intervention
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Behavioral: Mindful Self-Compassion
Mindful self-compassion is a course developed by Kristin Neff and Christopher Germer designed to cultivate self-compassion as measured by three subcategories: self-kindness, mindfulness, and a sense of common humanity. This study will shorten the original 8-week course to 5 sessions, and will include interventions and lectures aimed directly toward addressing evaluative concerns perfectionism. |
- Change in perfectionism [ Time Frame: Baseline (two for control group), one week prior to intervention, every week for four weeks until completion of intervention (including one week after last session), 6 months after intervention ]Adaptive perfectionism as measured by the "Personal Standards" subscale and maladaptive perfectionism/evaluative concerns perfectionism as measured by "Doubts about Actions" and "Concern over Mistakes" subscales of the Frost Multidimensional Perfectionism Scale. Personal Standards consists of seven items (6 items for "pure personal standards"), Doubt about Actions consists of four items, and Concern over Mistakes consists of 9 items. All items are on a 5-point Likert scale ranging from strongly disagree to disagree with higher scores indicating most perfectionistic tendencies. Full range: 20-100 with higher scores representing more perfectionistic tendencies. Evaluative concerns perfectionism range: 13-65, higher scores indicate more evaluative concerns perfectionism. Personal standards range: 7-35 with higher scores indicating higher personal standards.
- Change in body image [ Time Frame: Baseline (two for control group), one week prior to intervention, one week after last session, 6 months after intervention ]Body image as measured by the 13 item Body Appreciation Scale consisting of a 5-point Likert scale. Range: 13-65, lower scores indicating no body appreciation and higher scores indicating greater body appreciation.
- Change in depressive tendencies [ Time Frame: Baseline (two for control group), one week prior to intervention, every week for four weeks until completion of intervention (including one week after last session), 6 months after intervention ]Depressive tendencies as measured by the 12 item Major Depression Inventory which measures symptoms of depression on a 6-point Likert scale (not at all to all of the time), range: 12-72, with higher scores indicating more symptoms of depression.
- Change in anxiety [ Time Frame: Baseline (two for control group), one week prior to intervention, every week for four weeks until completion of intervention (including one week after last session), 6 months after intervention ]Anxiety as measured by the 20 item "trait subscale" of the State and Trait Anxiety Inventory. The Inventory consists of a 4-point Likert scale (almost never to almost always), range: 20-80, higher scores indicating greater anxiety.
- Change in self-compassion [ Time Frame: Baseline (two for control group), one week prior to intervention, every week for four weeks until completion of intervention (including one week after last session), 6 months after intervention ]Assessment of self-compassion with the Self-Compassion Scale short form.Total score range from 12 (no self-compassion) to 60 (high on self-compassion). Higher values represent greater self-compassion, lower scores indicate no self-compassion.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- College/university students
Exclusion Criteria:
- N/A
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03453437
| Norway | |
| University of Bergen | |
| Bergen, Hordaland, Norway, 5020 | |
| Principal Investigator: | Per-Einar Binder, PhD | University of Bergen |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | University of Bergen |
| ClinicalTrials.gov Identifier: | NCT03453437 |
| Other Study ID Numbers: |
UiBMSC2018 |
| First Posted: | March 5, 2018 Key Record Dates |
| Last Update Posted: | August 17, 2021 |
| Last Verified: | August 2021 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Depression Behavioral Symptoms |

