Clinical Trials Logo
  1. Home
  2. Infertility, Female
  3. NCT06181890
  4. Details
NCT06181890 Clinical Trial

The Effect of Motivational Interviews

Infertility, Female Clinical Trial

Official title:
The Effect of Motivational Interviews Applied to Infertile Women on Infertility Affect, Self-Efficacy and Coping With Stress

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT06181890
Other study ID # KSIU-SBF-ES-01
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date October 25, 2023
Est. completion date June 25, 2024

Study information
Verified date December 2023
Source Kahramanmaras Sutcu Imam University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study was to determine the effect of motivational interviews applied to infertile women on their ability to cope with infertility, self-efficacy and stress.

Description:

There is no study in the literature on the effectiveness of motivational interviewing on being affected by infertility, self-efficacy and coping with stress. It is important for healthcare personnel to be easy to apply and short-term, to be aware of the effectiveness of the motivational interviewing technique, and to use this technique in communicating with the patient and changing behavior. Based on these, it was deemed necessary to examine the effect of motivational interviews for infertile women.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 84
Est. completion date June 25, 2024
Est. primary completion date June 25, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Ages 18 and over and have no problems communicating Those who have not previously or currently been diagnosed with a psychiatric disease Infertile women who volunteer will be included in the sample of the research Exclusion Criteria: - Pregnancy during the study, Having previously or currently participated in a motivational interviewing program, Those who want to leave the research, Not completing motivational interviewing sessions, Infertile women with any deficiencies or errors in any of the forms from which the data are obtained will be excluded from the sample.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Motivational Interview
The data of the research will be collected between October 2023 and June 2024. Each meeting will last approximately 15-30 minutes.

Locations
Country Name City State
Turkey Eda Sever Kahramanmaras Onikisubat

Sponsors (1)
Lead Sponsor Collaborator
Kahramanmaras Sutcu Imam University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary motivational interview A total of 4 sessions of motivational interviews will be held for infertile women, 1 session per week for four weeks. 1 month
See also
  Status Clinical Trial Phase
Recruiting NCT05969574 - Is Decreased Ovarian Reserve Related to an Increased Number of Previous Early Miscarriages?
Recruiting NCT05358483 - PROspective Study of Mothers' and Infants' Social and Epidemiologic Determinants of Health
Recruiting NCT05969795 - Comparison of Live Birth Rate in Natural Cycle Single Euploid FET Versus Without Luteal Phase Support Phase 1
Recruiting NCT06051201 - Innovation for Small-scale Experiments: ReceptIVFity Test N/A
Completed NCT03177538 - Corifollitropin Alfa Combined With Menotropin Versus Follitropin and Lutropin Alfa in Expected Suboptimal Responders Phase 4
Completed NCT03638856 - Comparing Effectiveness of Oral Misoprostal for Cervical Priming in Hysteroscopy N/A
Completed NCT04052464 - The Study of the Implantation Window From Endometrial Biopsy With Gene Expression Methods
Withdrawn NCT04753736 - Immunophenotypage of RIF and RM Patients and Intrauterine Administration of PBMC N/A
Completed NCT03349905 - Deferred Versus Fresh Embryo Transfers N/A
Completed NCT05076981 - Progesterone Levels During Ovulation and Luteal Phase
Completed NCT04096027 - Cabergoline Before or After Oocyte Collection for Follicular Resolution Phase 4
Recruiting NCT05980091 - Optimal Timing of Euploid Day 6 Blastocyst Transfer in Frozen HRT Cycles, Day 6 or Day 7 of Progesterone Administration. Phase 1
Terminated NCT01933633 - Improved Fertility After Exercise in Overweight/Obese Women N/A
Completed NCT01202656 - Effect of Colony Stimulating Factor on Implantation and Pregnancy Rates Following IVF (in Vitro Fertilization) Phase 1/Phase 2
Terminated NCT01202643 - Effect of Colony Stimulating Factor on Poor Endometrial Development During IVF Phase 1/Phase 2
Completed NCT01408615 - A Post Marketing Observational Study of the Safety and Efficacy of Elonva (Corifollitropin Alfa) in General Practice (P08165)
Enrolling by invitation NCT05698550 - The Role of Erzhi Tiangui Formula in Expected POR Women Undergoing IVF-ET Phase 3
Not yet recruiting NCT03910582 - Personalized FET in RIF Patients With Displaced Dating N/A
Completed NCT05440019 - Evaluation of the Safety and Usability of the M3T Fertigo System and Its Calibration
Completed NCT05130125 - Retrospective Cohort Observational Study to Evaluate the Effectiveness and Safety of Fresh or Frozen Embryo Transfer