Anxiety Clinical Trial
Official title:
Mindful Self-Compassion (MSC) as an Intervention for Infertility Related Distress: A Pilot Study
This study will test a psychological intervention for the treatment of distress related to infertility. The intervention will pair reading a book "The Mindful Self-Compassion Workbook" by Kristin Neff with guided meditations using the Centre for Mindfulness Studies mobile app. Individuals with infertility will complete the 8-week program and complete psychological outcome measures before and after.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | May 1, 2022 |
Est. primary completion date | March 1, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 42 Years |
Eligibility | Inclusion Criteria: - Female - Undergoing fertility treatments or who have failed to conceive despite a 12 month period without the use of contraception - Reporting distress related to infertility, as indicated by Fertility Quality of Life Questionnaire score below 70, which is indicative of below-average quality of life Exclusion Criteria: - Currently seeking psychological treatment - Participation in a formal mindfulness program within 6 months of recruitment - Endorsement of active suicidal ideation, indicated by a score of 8 or above on the Suicidal Behaviors Questionnaire - GAD-7 score of 15-21, indicating severe generalized anxiety - PHQ-9 score of 20-27, indicating severe depressive symptoms. |
Country | Name | City | State |
---|---|---|---|
Canada | University of Regina | Regina | Saskatchewan |
Lead Sponsor | Collaborator |
---|---|
University of Regina |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Trait mindfulness | Scores on the FFMQ-15 (Five Facet Mindfulness Questionnaire-15) - scores range from 3 to 15 and higher scores indicate higher levels of mindfulness | Immediately post-intervention | |
Other | Trait mindfulness | Scores on the FFMQ-15 (Five Facet Mindfulness Questionnaire-15) - scores range from 3 to 15 and higher scores indicate higher levels of mindfulness | 1 month post-intervention | |
Other | Trait self-compassion | Scores on the SCS (Self-Compassion Scale) - scores range from 1 to 5, with higher scores indicating higher self-compassion | Immediately post-intervention | |
Other | Trait self-compassion | Scores on the SCS (Self-Compassion Scale) - scores range from 1 to 5, with higher scores indicating higher self-compassion | 1 month post-intervention | |
Other | Relationship quality | Scores on the RDAS (Revised Dyadic Adjustment Scale) - scores range from 0 to 69 and higher scores indicate better relationship quality | Immediately post-intervention | |
Other | Relationship quality | Scores on the RDAS (Revised Dyadic Adjustment Scale) - scores range from 0 to 69 and higher scores indicate better relationship quality | 1 month post-intervention | |
Primary | Fertility-related quality of life | Score on the FertiQoL (fertility-related Quality of Life tool) - scores range from 0 to 100 and higher scores indicate better quality of life | Immediately post-intervention | |
Primary | Fertility-related quality of life | Score on the FertiQoL (fertility-related Quality of Life tool) - scores range from 0 to 100 and higher scores indicate better quality of life | 1 month post-intervention | |
Secondary | Anxious symptoms | Scores on the GAD-7 (Generalized Anxiety Disorder-7) - scores range from 0 to 21 and higher scores indicate more severe anxiety | Immediately post-intervention | |
Secondary | Anxious symptoms | Scores on the GAD-7 (Generalized Anxiety Disorder-7) - scores range from 0 to 21 and higher scores indicate more severe anxiety | 1 month post-intervention | |
Secondary | Depressive symptoms | Scores on the PHQ-9 (Patient History Questionnaire-9) - scores range from 0 to 27 and higher scores indicate more severe symptoms | Immediately post-intervention | |
Secondary | Depressive symptoms | Scores on the PHQ-9 (Patient History Questionnaire-9) - scores range from 0 to 27 and higher scores indicate more severe symptoms | 1 month post-intervention |
Status | Clinical Trial | Phase | |
---|---|---|---|
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