Meditation and Mindfulness for Recurrent Pregnancy Loss
Primary Purpose
Recurrent Pregnancy Loss
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Meditation and mindfulness
Sponsored by
About this trial
This is an interventional treatment trial for Recurrent Pregnancy Loss focused on measuring Meditation, mindfulness, pregnancy loss, stress
Eligibility Criteria
Inclusion Criteria:
- Women with RPL
- Speaking, reading and understanding Danish
- Have given a written consent
- Have a male partner
- Have a stress score > 16 points on Perceived Stress Scale
Exclusion Criteria:
- If the patient is pregnant on inclusion day
- If the patient already is practing meditation and mindfulness
- If the patient has a depression
- If the patient develops a depression after inclusion in either arm
Sites / Locations
- RigshospitaletRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Meditation and mindfulness intervention
Control group
Arm Description
Women in the intervention arm will 3 times receive a three hours work shop with introduction to meditation and mindfulness over a 7 week period from a certified meditation instructor. Questionnaires before and after the intervention.
Women in the no intervention arm will receive no introduction to meditation and mindfulness - only questionnaires at the same time as the intervention group receives questionnaires.
Outcomes
Primary Outcome Measures
Perceived Stress Scale (PSS)
Change from baseline to 7 weeks after date of first course day measured by Perceived Stress Scale. PSS is a validated 10-item-self-reporting scale for stress symptoms. The 5 point Likert scale ranges from 0 (no stress) to 40 (extreme stress). The higher score the more stress.
Perceived Stress Scale (PSS)
Change from baseline to 12 months after date of first course day measured by the Perceived Stress Scale. PSS is a validated 10-item-self-reporting scale for stress symptoms. The 5 point Likert scale ranges from 0 (no stress) to 40 (extreme stress). The higher score the more stress.
Secondary Outcome Measures
COMPI Fertility Problem Stress Scale
Change from baseline to 7 weeks after date of first course day using the COMPI Fertility Problem Stress Scale.
The COMPI Fertility Problem Stress Scale is a validated scale measuring the impact of RPL on the woman and her interpersonal relationships. Two questions asking if the experience of RPL has been stressful for the woman with five answering options. Followed by seven sub questions asking how big a load RPL has been for the patients interpersonal life with four answering options. The lower the score the higher stress.
Marital Benefit Scale
Change in marital benefit from baseline to 7 weeks after date of first course day using the COMPI Marital Benefit Scale.
The COMPI Marital Benefit Scale has two questions asking what the RPL have mattered for their relationship/mariage:
Five options to answer: totally disagree, partly disagree, neither agree or disagree, partly agree, totally agree. Answering "Totally agree" on both questions is defined as a high marital benefit.
COMPI Fertility Problem Stress Scale
Change in fertility problem stress from baseline to 12 months after date of first course day using the COMPI Fertility Problem Stress Scale.
The COMPI Fertility Problem Stress Scale is a validated scale measuring the impact of RPL on the woman and her interpersonal relationships. Two questions used to assess how big a impact RPL has for the patient with five answering options. Followed by seven sub questions asking how big a load RPL has been for the patients interpersonal life with four answering options. The lower the score the higher stress.
Marital Benefit
Change in marital benefit from baseline to 12 months after date of first course day using the COMPI Marital Benefit Scale.
The COMPI Marital Benefit Scale has two questions asking what the RPL have mattered for their relationship/mariage:
Five options to answer: totally disagree, partly disagree, neither agree or disagree, partly agree, totally agree. Answering "Totally agree" on both questions is defined as a high marital benefit.
Major Depression Index (MDI)
Change in depression score from baseline to 12 months after date of first course day. Major Depression Index is a validated self-rating depression scale, which is used both clinically and in epidemiological studie. The 6-point Likert scale ranges from 0 (no depression) to 50 (extreme depression).
Full Information
NCT ID
NCT03905395
First Posted
April 2, 2019
Last Updated
April 4, 2019
Sponsor
Henriette Svarre Nielsen, MD, DMSc
1. Study Identification
Unique Protocol Identification Number
NCT03905395
Brief Title
Meditation and Mindfulness for Recurrent Pregnancy Loss
Official Title
Meditation and Mindfulness for Recurrent Pregnancy Loss
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 2, 2019 (Actual)
Primary Completion Date
June 30, 2020 (Anticipated)
Study Completion Date
June 30, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Henriette Svarre Nielsen, MD, DMSc
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In the Danish Recurrent Pregnancy Loss Unit in Rigshospitalet in Copenhagen recurrent pregnancy loss (RPL) is defined as three og more consecutive pregnancy losses in accordance with current European guidelines.
RPL affects approximately 3% of couples trying to achieve parenthood. Most cases of RPL are unexplained and have no effective treatment to improve the chance of a live birth.
42% of the women referred to RPL Unit in Rigshospitalet has a high stress level where as it's 22% in the background population trying to achieve parenthood. It's also known that 8,8 % of RPL patients have a depression at referral where as it's 2,2 % in the background population trying to achieve parenthood.
The study is a RCT including 62 patients - 31 in each arm. One arm will be taught in meditation and mindfulness three courses over a 7 week period. This group will also do meditation every day for 7 weeks. The other arm will have no intervention.
This study will investigate if a 7 weeks course in meditation and mindfulness is a useful tool to reduce stress and the psychological consequences for women and their partner treated in RPL Unit in Rigshospitalet, Copenhagen. Furthermore this study will investigate if there's a marital benefit such as reinforcement in their relationsship from practicing meditation and mindfulness.
There is no previous study that has investigated meditation and mindfulness for RPL.
This study has the potential to establish mental health support as a supplement to the medical and clinical treatment for RPL patients.
Detailed Description
The loss of a desired pregnancy is a significant negative life event associated with grief comparable to the grief after a peri- or neonatal death. Recurrent pregnancy loss (RPL) defined as 3 or more pregnancy losses affects approximately 3% of couples trying to have children. Most cases of RPL are unexplained and have no effective treatment to improve the chance of a live birth.
42% of the women referred to RPL Unit in Rigshospitalet has a high stress level where as it's 22% in the background population trying to achieve parenthood. It's also known that 8,8% of RPL patients have a depression at referral where as it's 2,2 % in the background population trying to achieve parenthood.
This study will investigate if a 7 weeks course in meditation and mindfulness is a useful tool to reduce stress and the psychological consequences for women and their partner treated in RPL Unit in Rigshospitalet, Copenhagen.
Furthermore this study will investigate if there's a marital benefit from practicing meditation and mindfulness. The investigators will use four different scales to measure the participants stress, depression, marital benefit and fertility stress. Also the investigators will measure the participants before and after the intervention and 12 months after.
All participants will have to complete:
Major Depression Index, a validated self-rating depression scale, which is used both clinically and in epidemiological studie. The 6-point Likert scale ranges from 0 (no depression) to 50 (extreme depression).
Perceived Stress Scale, which is a validated 10-item-self-reporting scale for stress symptoms. The 5 point Likert scale ranges from 0 (no stress) to 40 (extreme stress).
The COMPI Fertility Problem Stress Scale, a validated scale measuring the impact of RPL on the woman and her interpersonal relationships.
The COMPI Marital Benefit Scale measuring if RPL has reinforced the couples mariage/relationship.
The investigators assume that meditation and mindfulness can improve the quality of life for the RPL patients and their coping strategies. It's the investigators purpose to contribute with new knowledge in this area for current and future patients.
The RPL Unit in Rigshospitalet doesn't have any psychological support apart from ordinary attention from the nurses. This study has the potential to establish mental health support as a supplement to the medical and clinical treatment for RPL patients, which is in high demand.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Pregnancy Loss
Keywords
Meditation, mindfulness, pregnancy loss, stress
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized trial where women in an experimental arm will receive 3 times a three hour work shop with introduction to meditation and mindfulness during a 7 week period. Women in the other arm will have no intervention.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Meditation and mindfulness intervention
Arm Type
Active Comparator
Arm Description
Women in the intervention arm will 3 times receive a three hours work shop with introduction to meditation and mindfulness over a 7 week period from a certified meditation instructor. Questionnaires before and after the intervention.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Women in the no intervention arm will receive no introduction to meditation and mindfulness - only questionnaires at the same time as the intervention group receives questionnaires.
Intervention Type
Behavioral
Intervention Name(s)
Meditation and mindfulness
Intervention Description
Women in the intervention arm will 3 times receive a three hours work shop with introduction to meditation and mindfulness over a 7 week period from a certified meditation instructor. Questionnaires before and after the intervention.
Primary Outcome Measure Information:
Title
Perceived Stress Scale (PSS)
Description
Change from baseline to 7 weeks after date of first course day measured by Perceived Stress Scale. PSS is a validated 10-item-self-reporting scale for stress symptoms. The 5 point Likert scale ranges from 0 (no stress) to 40 (extreme stress). The higher score the more stress.
Time Frame
7 weeks
Title
Perceived Stress Scale (PSS)
Description
Change from baseline to 12 months after date of first course day measured by the Perceived Stress Scale. PSS is a validated 10-item-self-reporting scale for stress symptoms. The 5 point Likert scale ranges from 0 (no stress) to 40 (extreme stress). The higher score the more stress.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
COMPI Fertility Problem Stress Scale
Description
Change from baseline to 7 weeks after date of first course day using the COMPI Fertility Problem Stress Scale.
The COMPI Fertility Problem Stress Scale is a validated scale measuring the impact of RPL on the woman and her interpersonal relationships. Two questions asking if the experience of RPL has been stressful for the woman with five answering options. Followed by seven sub questions asking how big a load RPL has been for the patients interpersonal life with four answering options. The lower the score the higher stress.
Time Frame
7 weeks
Title
Marital Benefit Scale
Description
Change in marital benefit from baseline to 7 weeks after date of first course day using the COMPI Marital Benefit Scale.
The COMPI Marital Benefit Scale has two questions asking what the RPL have mattered for their relationship/mariage:
Five options to answer: totally disagree, partly disagree, neither agree or disagree, partly agree, totally agree. Answering "Totally agree" on both questions is defined as a high marital benefit.
Time Frame
7 weeks
Title
COMPI Fertility Problem Stress Scale
Description
Change in fertility problem stress from baseline to 12 months after date of first course day using the COMPI Fertility Problem Stress Scale.
The COMPI Fertility Problem Stress Scale is a validated scale measuring the impact of RPL on the woman and her interpersonal relationships. Two questions used to assess how big a impact RPL has for the patient with five answering options. Followed by seven sub questions asking how big a load RPL has been for the patients interpersonal life with four answering options. The lower the score the higher stress.
Time Frame
12 months
Title
Marital Benefit
Description
Change in marital benefit from baseline to 12 months after date of first course day using the COMPI Marital Benefit Scale.
The COMPI Marital Benefit Scale has two questions asking what the RPL have mattered for their relationship/mariage:
Five options to answer: totally disagree, partly disagree, neither agree or disagree, partly agree, totally agree. Answering "Totally agree" on both questions is defined as a high marital benefit.
Time Frame
12 months
Title
Major Depression Index (MDI)
Description
Change in depression score from baseline to 12 months after date of first course day. Major Depression Index is a validated self-rating depression scale, which is used both clinically and in epidemiological studie. The 6-point Likert scale ranges from 0 (no depression) to 50 (extreme depression).
Time Frame
12 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Based on biological sex
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
46 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women with RPL
Speaking, reading and understanding Danish
Have given a written consent
Have a male partner
Have a stress score > 16 points on Perceived Stress Scale
Exclusion Criteria:
If the patient is pregnant on inclusion day
If the patient already is practing meditation and mindfulness
If the patient has a depression
If the patient develops a depression after inclusion in either arm
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Henriette Svarre Nielsen, MD, DMSc
Phone
+4535458486
Email
Henriette.Svarre.Nielsen@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Karen Henriette Kirchheiner Jensen, Nurse
Phone
+4535458486
Email
Karen.Henriette.jensen@regionh.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen Kirchheiner Jensen, Nurse
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Study Director
Facility Information:
Facility Name
Rigshospitalet
City
Copenhagen
State/Province
Østerbro
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Henriette Svarre Nielsen, MD. MDSc
Phone
+4535458486
Email
Henriette.Svarre.Nielsen@regionh.dk
First Name & Middle Initial & Last Name & Degree
Karen Kirchheiner Jensen, Nurse
Phone
+4535458486
Email
Karen.Henriette.Jensen@regionh.dk
12. IPD Sharing Statement
Plan to Share IPD
No
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Meditation and Mindfulness for Recurrent Pregnancy Loss
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