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The Effect of the Mind/Body Program for Fertility, Hungarian Version, on Well-Being and Assisted Reproduction Outcomes

Primary Purpose

Infertility, Female

Status
Active
Phase
Not Applicable
Locations
Hungary
Study Type
Interventional
Intervention
Mind/Body Program for Fertility (Domar et al., 2011)
Fertility Support Program
Sponsored by
Semmelweis University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Infertility, Female focused on measuring female infertility, assisted reproductive technology, in vitro fertilization, intra-cytoplasmic sperm injection, pregnancy, stress, depression, anxiety, quality of life, sleep quality, circadian rhythm, mind/body

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: All women awaiting or undergoing infertility treatment (insemination, in vitro fertilization or intracytoplasmic sperm injection) at the Assisted Reproduction Center of the Department of Obstetrics and Gynecology at Semmelweis University, Budapest, who:

  • give informed consent to participating in the study
  • have sufficient knowledge of the Hungarian language

Exclusion Criteria:

  • active psychotic episode
  • severe depression or other major psychiatric diagnoses
  • substance abuse
  • eating disorders

Sites / Locations

  • Assisted Reproduction Center of the Department of Obstetrics and Gynecology at Semmelweis University
  • Institute of Behavioral Sciences at Semmelweis University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mind/Body Group

Support Group

Arm Description

All persons allocated to the intervention group will take part in a 10-week Mind/Body skills development fertility program parallel with fertility workup and treatment.

All persons allocated to the comparison intervention group will take part in a 10-week fertility support program parallel with fertility workup and treatment.

Outcomes

Primary Outcome Measures

Mean change from baseline in results on the Fertility Quality of Life tool
Mean change from baseline in results on the Fertility Quality of Life (FertiQoL) Core Scale, subscales and Treatment Module
Mean change from baseline in results on the SCREENIVF tool
Mean change from baseline in results on the SCREENIVF tool and its subscales
Clinical pregnancy
Rate of clinical pregnancies at post-measurement

Secondary Outcome Measures

Mean change from baseline on a Likert scale measuring strength of intention to continue treatment
Mean change from baseline on a 10-point Likert scale measuring strength of intention to continue treatment (if first ART cycle not successful) to post-measurement

Full Information

First Posted
October 28, 2019
Last Updated
May 2, 2023
Sponsor
Semmelweis University
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1. Study Identification

Unique Protocol Identification Number
NCT04151485
Brief Title
The Effect of the Mind/Body Program for Fertility, Hungarian Version, on Well-Being and Assisted Reproduction Outcomes
Official Title
The Effect of the Mind/Body Program for Fertility, Hungarian Version, on Psychological Well-Being and Assisted Reproduction Technology (ART) Outcomes: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 15, 2019 (Actual)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
August 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Semmelweis University

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
Involuntary childlessness is an emotionally stressful experience; however, psychosocial counseling is typically not available in Hungarian routine fertility care. The aim of this randomized controlled trial (RCT) is to examine the effectiveness of a Mind/Body psychological fertility intervention for women in reproductive treatment. We hypothesize that participants of the Mind/Body Program for Fertility, Hungarian version, will have more favorable psychological well-being, ART outcome results than participants of the Fertility Support Groups.
Detailed Description
Involuntary childlessness imposes significant psychological burden on those affected, particularly those involved in assisted reproductive technology (ART). The reduction of psychological distress has been shown to improve the quality of life of those affected and to possibly increase chances of pregnancy. While in more developed countries psychological support is largely available in routine fertility care, it is not yet part of the Hungarian ART protocol. In this study, the effects of a psychosocial intervention, namely, the Hungarian version of the Mind/Body Program for Fertility (Domar et al., 2011), will be tested on the psychological well-being and ART outcomes of women in reproductive treatment, in a randomized controlled pre-post design. For this purpose, women in ART treatment will fill in screening questionnaires (on depression, anxiety, stress, etc.), and moderate to high scorers will be randomized into an intervention (Mind/Body) group (N=70) and a comparison intervention (Fertility Support) group (N=70), lasting for 10 weeks each, before and/or during an ART cycle. Both interventions will be delivered by the same clinical psychologist, listed as central contact person below, officially trained in the Mind/Body Program for Fertility by Dr. Alice Domar at Boston IVF, Waltham, Massachusetts. A smartphone application for rating subjective stress levels twice a day, from the start of the stimulation to the day of the pregnancy test, will also be administered. Additionally, whole-night sleep EEGs will be recorded. Medical data (such as diagnosis, hormone levels, previous treatment cycles, etc.) and sociodemographic (such as age, education, etc.) and psychological variables (such as personality traits, chronotype, intelligence, etc.) as potential moderators, as well as ART outcomes will be reported. Data of respondents willing to fill in pre- and post-questionnaires but 1) not motivated to take part in the study, or 2) motivated to take part in the study, but not able to make it, will be registered but excluded from statistical analysis comparing RCT results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female
Keywords
female infertility, assisted reproductive technology, in vitro fertilization, intra-cytoplasmic sperm injection, pregnancy, stress, depression, anxiety, quality of life, sleep quality, circadian rhythm, mind/body

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Mind/Body and Fertility Support Groups will be running in a parallel manner, with continuous enrollment on the basis of pre-generated random number tables. Each group will consist of 10-16 members, and run for 10 weeks. Every 11th week two new groups (one Mind/Body and one Fertility Support) will be scheduled, and so on, until the desired number of participants will be collected.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participants, statisticians and medical staff will be blinded for intervention allocation. Since, to control the therapist variable, the two types of interventions will be done by the same person, blinding on the Care Provider's part is not possible.
Allocation
Randomized
Enrollment
177 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mind/Body Group
Arm Type
Experimental
Arm Description
All persons allocated to the intervention group will take part in a 10-week Mind/Body skills development fertility program parallel with fertility workup and treatment.
Arm Title
Support Group
Arm Type
Active Comparator
Arm Description
All persons allocated to the comparison intervention group will take part in a 10-week fertility support program parallel with fertility workup and treatment.
Intervention Type
Behavioral
Intervention Name(s)
Mind/Body Program for Fertility (Domar et al., 2011)
Intervention Description
see Arm Description
Intervention Type
Behavioral
Intervention Name(s)
Fertility Support Program
Intervention Description
see Arm Description
Primary Outcome Measure Information:
Title
Mean change from baseline in results on the Fertility Quality of Life tool
Description
Mean change from baseline in results on the Fertility Quality of Life (FertiQoL) Core Scale, subscales and Treatment Module
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the SCREENIVF tool
Description
Mean change from baseline in results on the SCREENIVF tool and its subscales
Time Frame
through study completion, an average of 2 years
Title
Clinical pregnancy
Description
Rate of clinical pregnancies at post-measurement
Time Frame
through study completion, an average of 2 years
Secondary Outcome Measure Information:
Title
Mean change from baseline on a Likert scale measuring strength of intention to continue treatment
Description
Mean change from baseline on a 10-point Likert scale measuring strength of intention to continue treatment (if first ART cycle not successful) to post-measurement
Time Frame
through study completion, an average of 2 years
Other Pre-specified Outcome Measures:
Title
Mean change from baseline in results on the Beck Depression Inventory
Description
Mean change from baseline in results on the 21-item Beck Depression Inventory (BDI), with special attention to category change (e.g. from moderate to mild depression level, from mild to no depression)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the World Health Organisation-Five Well-Being Index
Description
Mean change from baseline in results on the 5-item World Health Organisation-Five Well-Being Index (WHO-5)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Spielberger State-Trait Anxiety Inventory
Description
Mean change from baseline in results on the State and Trait subscales of the Spielberger State Trait Anxiety Inventory (STAI)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Short Stress Scale
Description
Mean change from baseline in results on the 26-item Short Stress Scale (SSS)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Perceived Stress Scale
Description
Mean change from baseline in results on the 10-item Perceived Stress Scale (PSS-10)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Life Meaning subscale of the Brief Stress and Coping Inventory
Description
Mean change from baseline in results on the 7-item Life Meaning subscale of the Brief Stress and Coping Inventory (BSCI-LM)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Awareness of Mind-Body Integration and the Trusting Body Sensations subscales of the Multidimensional Assessment of Interoceptive Awareness
Description
Mean change from baseline in results on the 12-item Awareness of Mind-Body Integration and the 3-item Trusting Body Sensations subscales of the Multidimensional Assessment of Interoceptive Awareness (MAIA)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Fertility Problem Stress Scales and the Coping Strategy Scales of the Copenhagen Multi-centre Psychosocial Infertility study questionnaire
Description
Mean change from baseline in results on the 14-item Fertility Problem Stress Scales and the 19-item Coping Strategy Scales of the Copenhagen Multi-centre Psychosocial Infertility (COMPI) study questionnaire
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Sexual Concerns subscale of the Fertility Problem Inventory
Description
Mean change from baseline in results on the 8-item Sexual Concerns subscale of the Fertility Problem Inventory
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Relationship Assessment Scale
Description
Mean change from baseline in results on the 7-item Relationship Assessment Scale (RAS)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Pittsburgh Sleep Quality Index
Description
Mean change from baseline in results on the Pittsburgh Sleep Quality Index (PSQI)
Time Frame
through study completion, an average of 2 years
Title
Mean change from baseline in results on the Athens Insomnia Scale
Description
Mean change from baseline in results on the 8-item Athens Insomnia Scale (AIS)
Time Frame
through study completion, an average of 2 years
Title
Mean results on a smartphone-based Likert-scale rating momentary stress
Description
Mean results on the StressFlash smartphone-based Likert-scale rating momentary stress
Time Frame
through study completion, an average of 2 years
Title
Number of oocytes retrieved
Description
Number of oocytes retrieved at transvaginal oocyte retrieval (TVOR)
Time Frame
through study completion, an average of 2 years
Title
Number of oocytes fertilized
Description
Number of oocytes fertilized via IVF/ICSI
Time Frame
through study completion, an average of 2 years
Title
Number of embryos transferred
Description
Number of embryos transferred at embryo transfer (ET)
Time Frame
through study completion, an average of 2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All women awaiting or undergoing infertility treatment (insemination, in vitro fertilization or intracytoplasmic sperm injection) at the Assisted Reproduction Center of the Department of Obstetrics and Gynecology at Semmelweis University, Budapest, who: give informed consent to participating in the study have sufficient knowledge of the Hungarian language Exclusion Criteria: active psychotic episode severe depression or other major psychiatric diagnoses substance abuse eating disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
György Purebl, PhD Ass.Prof
Organizational Affiliation
Institute of Behavioural Sciences, Semmelweis University, Budapest
Official's Role
Principal Investigator
Facility Information:
Facility Name
Assisted Reproduction Center of the Department of Obstetrics and Gynecology at Semmelweis University
City
Budapest
ZIP/Postal Code
1082
Country
Hungary
Facility Name
Institute of Behavioral Sciences at Semmelweis University
City
Budapest
ZIP/Postal Code
1089
Country
Hungary

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21496800
Citation
Domar AD, Rooney KL, Wiegand B, Orav EJ, Alper MM, Berger BM, Nikolovski J. Impact of a group mind/body intervention on pregnancy rates in IVF patients. Fertil Steril. 2011 Jun;95(7):2269-73. doi: 10.1016/j.fertnstert.2011.03.046. Epub 2011 Apr 15.
Results Reference
background

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The Effect of the Mind/Body Program for Fertility, Hungarian Version, on Well-Being and Assisted Reproduction Outcomes

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