- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT05148273
The Effect of Telehealth Applications on the Level of Anxiety in the Treatment of Infertility
Investigation of the Effects of Telehealth Applications Applied to Infertile Women During Drug Treatment Procedures on Anxiety Levels: A Randomized Controlled Study
It is expected that 84% natural pregnancy will occur at the end of the first 12 months of sexual intercourse without the use of contraceptive methods.The lack of natural fertility is under the influence of multiple factors. These factors can be summarized as age, past infections, genetic factors, anatomical structural disorders, environmental toxins, occupational exposure, lifestyle and sexually transmitted infections.Severe psychological stress, anxiety and depression are encountered in the diagnosis, treatment method and management of the related process in couples who are faced with the diagnosis of infertility.
With the telehealth service that came to the fore in the world in the 1950s, nurses use it in the management of many treatment processes such as infertility treatment, with the roles of managing the information collection process, making decisions with the information they receive, and transmitting information on patients who are far away and need constant follow-up.
Assisted reproductive technologies, which are the current treatment method of infertility, have been used effectively for thirty years. Anxiety control is important in the success of treatment in the treatment process, which is both costly and stressful. Providing 24/7 hours of counseling by using telehealth methods contributes to the reduction of this anxiety.
Aperçu de l'étude
Description détaillée
Type d'étude
Inscription (Anticipé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Başak Demiralp Yavuz, nurse
- Numéro de téléphone: +902462113719 +905071721836
- E-mail: basakdemiralp1@gmail.com
Sauvegarde des contacts de l'étude
- Nom: Emel Taşçı Duran, Prof.Dr.
- E-mail: emelduran@sdu.edu.tr
Lieux d'étude
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Center, East Campus
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Isparta, Center, East Campus, Turquie, 32200
- Recrutement
- Suleyman Demırel Unıversıty research and practice hospital
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Contact:
- Başak Demiralp Yavuz, nurse
- Numéro de téléphone: +905071721836
- E-mail: basakdemiralp1@gmail.com
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Between the ages 20-45
- Female
- Having been diagnosed with infertility
- Should be able to use a smart phone
- Open to communication
Exclusion Criteria:
- Not between the ages of 20-45
- Individuals who do not want to be inherited
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
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intervention
After the selection process with 1 to 1 randomization method, a personal information form and Beck anxiety scale will be applied to the women selected for the case group on the day of the initiation of treatment with assisted reproductive techniques interview.
Then, within an average of 10 days, there is a treatment procedure including planned drug use, messages containing drug doses, drug use, drug administration, follicle count, reminder of the times of operations such as OPU, IUI, ET, and motivational issues.
Medication use, time, date, dose, application form and motivational sentences will be sent every day through the WhatsApp application.
The Beck anxiety scale will be repeated on the day of IUI and ET procedures, and the effect of telehealth practices on the anxiety levels of women undergoing infertility treatment will be evaluated.
During the study, the participants will be able to reach the researcher from their mobile phones whenever they want.
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7-24 counseling and daily treatment protocol reminders will be given to the intervention group.
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control
In the first interview at the beginning of the treatment protocol with assisted reproductive techniques, a personal information questionnaire and beck anxiety scale will be applied to the control group selected by the 1-to-1 randomization method.
Afterwards, the Beck anxiety scale will be applied again at the end of the treatment without any intervention.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
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beck anxiety scale
Délai: 1 year
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The intervention group will be evaluated with the Beck anxiety scale at the beginning of the treatment. Afterwards, the patient who was given telehealth service throughout the treatment will be compared by applying the Beck anxiety scale again at the end of the treatment. The control group will be compared by applying the Beck anxiety scale before and after the treatment. |
1 year
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: başak demiralp yavuz, nurse, Researcher
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Anticipé)
Achèvement de l'étude (Anticipé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- TELENURSING and anxıety
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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