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The Effect of a Mindset Management Approach on Stress Levels in Women With Infertility

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Primary completion date: Mar 2025 to Dec 2026
    • Study completion date: May 2025 to Dec 2026
    v6
  2. Notable Primary completion date: Jun 2024 to Mar 2025
    • Study completion date: Feb 2025 to May 2025
    v5
  3. Minor Study description shortened, about 30 wordsv4
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Primary completion date: Mar 2024 to Jun 2024
    • Start date changed from estimate of Oct 2023 to Nov 10, 2023
    v3
  5. Minor Start date: Sep 2023 to Oct 2023
    • Secondary endpoints revised (7)
    • Study description expanded, about 1,302 words
    v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to test the effect of a mindset management intervention on stress levels in women with infertility. The main question it aims to answer is: Can the Organic Conceptions approach decrease stress levels in women with infertility? Participants in both groups will be asked to complete three surveys at three time points. The intervention group will complete the Organic Conceptions program, while the control group will not complete an intervention. Researchers will compare the intervention group and control group to see if the Organic Conceptions mindset management program decreases stress levels in women with infertility.
Trial Details
NCT Number NCT05997407
Lead Sponsor Virginia Polytechnic Institute and State University
Collaborators: Shady Grove Fertility Reproductive Science Center
Conditions
(from sponsor)
Stress, Infertility, Female
Related terms Infertility, Female
Enrollment 66 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov