An Intervention on Psychosocial Health in Women With Unsuccessful IVF Experience

NCT ID: NCT06426472

Last Updated: 2025-04-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-30

Study Completion Date

2026-08-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Infertility Failed in Vitro Fertilisation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention

Interventional group which will be given the web-based fertility support

Group Type EXPERIMENTAL

Web-based support program

Intervention Type OTHER

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

Control

Control group will not be given any intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Web-based support program

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

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

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

Exclusion Criteria

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


1. Spontaneous pregnancy occurring,
2. Starting a new treatment cycle,
3. Not continuing to monitor the modules on the website.
Minimum Eligible Age

21 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Elif Balkan

PhD Student

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Elif Balkan, PhD Student

Role: CONTACT

+90 5423513125

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

1649B032306898

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

EBIstanbulUC

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Immune Modulators and IVF
NCT02626702 TERMINATED
Follicular Flushing
NCT01558141 COMPLETED NA