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Not yet recruiting NCT06426472

An Intervention on Psychosocial Health in Women With Unsuccessful IVF Experience

No phase Interventional Infertility Failed in Vitro Fertilisation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Web-based support program.
Who it may be relevant to
Registry conditions: Infertility, Failed in Vitro Fertilisation. Basic parameters: from 21 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Web-Based Support Program on Psychosocial Health Status in Women With Unsuccessful IVF Experience

Overview

The goal of this interventional study is to learn if web-based support program can improve the psychosocial health status in women with unsuccessful IVF experience. The main questions it aims to answer are: Does web-based support decrease the depressive symptoms, anxiety and infertility-related stress? Does web-based support decrease the hopelessness? Does web-based support increase the coping skills with infertility-related stress? Researchers will compare this intervention to a control group to see if web-based support program improves psychosocial health. Participants will: Use the web-based support intervention for 5 weeks or have no intervention. Complete the surveys on the website before and after the intervention.

Interventions

  • Other Web-based support program
    Web-based support program for infertile women with failed IVF experience

Primary outcome measures

  • Depression (Beck Depression Inventory) [Time frame: 24 months]
  • Infertility-related stress (The Infertility Stress Scale) [Time frame: 24 months]
  • Coping Skills with Infertility Stress (Coping with Infertility Stress Scale) [Time frame: 24 months]
Secondary outcome measures (2)
  • Hopelessness [Time frame: 24 months]
  • Effect of the Web-based study program [Time frame: 24 months]

Eligibility criteria

Inclusion criteria

  • Having at least three repeated unsuccessful IVF experiences,
  • Maximum one month has passed since the negative IVF experience,
  • Participating in the study voluntarily,
  • Being able to read, understand and communicate in Turkish.

Exclusion criteria

  • Not having access to the internet/not knowing how to use it,
  • Having any psychiatric disease/being in the 'severe depression' grade as a result of the Beck Depression Inventory,
  • Having at least one living child.

Exclusion criteria from the study in the stages after including the study:

  • Spontaneous pregnancy occurring,
  • Starting a new treatment cycle,
  • Not continuing to monitor the modules on the website.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06426472 · EBIstanbulUC · 1649B032306898

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗