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Clinical Trials/NCT03343405
NCT03343405
Completed
Not Applicable

Fertility & Well-Being: Mind/Body Protocol

University of Vermont1 site in 1 country71 target enrollmentMarch 14, 2015
ConditionsInfertility

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infertility
Sponsor
University of Vermont
Enrollment
71
Locations
1
Primary Endpoint
Feasibility 2: Time
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This pilot-study assesses the feasibility and acceptability of an Online Mind/Body Fertility Program, designed to help individuals and/or couples cope with the physical and emotional impact of infertility by learning special relaxation strategies and improving lifestyle habits. Participants included women experiencing infertility who had not given birth to a child. Half of participants received access to the 10-week Online Mind-Body Program and the other half were placed on a waiting-list.

Detailed Description

Infertility is defined as the inability to conceive a child. A couple may be acknowledged as infertile if conception has not occurred after 12 months of having regular, unprotected intercourse. Over six million couples in the United States are affected by infertility. Research suggests that there is a relationship between psychological distress and infertility, but the relationship is complex. The information from this study will be used to better understand the relationship between psychological distress and infertility among couples. Furthermore, the investigators are interested in testing Dr. Alice Domar's Mind/Body Fertility Program that was designed to help individuals regain control of their life and learn new lifestyle habits that can increase their chances of conceiving. There is evidence that individuals that participated in the group format of this treatment protocol showed statistically significant decreases in physical and psychological symptoms of stress and increases in conception rates. Our primary goals are to evaluate patients willingness to be recruited and randomized as well as their adherence and attrition to the program. Our secondary goals are to evaluate reductions in emotional distress (i.e., anxiety, depression, and stress) and enhance emotion regulation skills as well as pregnancy rates.

Registry
clinicaltrials.gov
Start Date
March 14, 2015
End Date
April 14, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jessica Clifton

Post-Doctoral Associate

University of Vermont

Eligibility Criteria

Inclusion Criteria

  • Women and Men
  • Infertility diagnosis
  • Trying to get pregnant
  • 18 years or older
  • Read and write English

Exclusion Criteria

  • No current diagnosis for an active psychotic disorder, eating disorder, substance abuse or dependence
  • Not reporting current suicidal ideation/intent
  • No psychotropic medication changes in the last four weeks
  • Has not completed a formal mind/body program focused on infertility that included relaxation, yoga, mindfulness, cognitive restructuring, stress reduction strategies, listening and communication skills, goal setting and assertiveness training.

Outcomes

Primary Outcomes

Feasibility 2: Time

Time Frame: Approximately 12 months

Time between recruitment and completion of the study. Time between recruitment and randomization; time between each of the modules; time between each of the assessments (pre-assessment; mid-assessment; post-assessment, and follow-up).

Feasibility 1: Feasibility of recruitment and randomization

Time Frame: Approximately 12 months

Number of participants recruited and randomized. From time study began to when recruitment closed.

Feasibility 3: Participant retention and acceptability

Time Frame: Approximately 12 months

Percentage of enrolled participants that completed each stage of the study (mid-assessment, post-assessment, follow-up, and each of the ten modules for the intervention group only).

Secondary Outcomes

  • Acceptability 1: Ease of modules(Approximately 12 months)
  • Acceptability 2: Helpfulness(Approximately 12 months)
  • Satisfaction of Intervention(Approximately 12 months)
  • Fertility Problem Inventory: Between group changes(Approximately 12 months)
  • Emotion Regulation: Between group comparison(Approximately 12 months)
  • Relationship Quality: Between group comparison(Approximately 12 months)
  • Pregnancy: Between group comparison(Approximately 12 months)
  • Anxiety 2: Between group changes(Approximately 12 months)
  • Depression 1: Individual changes(Approximately 12 months)
  • Stress: Between group changes(Approximately 12 months)
  • Anxiety 1: Individual changes(Approximately 12 months)
  • Depression 2: Between group changes(Approximately 12 months)
  • Mindfulness: Between group comparison(Approximately 12 months)

Study Sites (1)

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