- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03236402
"A Study to Assess Knowledge and Opinion Regarding Adoption Among Adults Residing in Rural and Urban Area"
"A Cross-sectional Comparative Study to Assess Knowledge and Opinion Regarding Adoption Among Adults Residing in Rural and Urban Area of Ambala, Haryana"
Aperçu de l'étude
Statut
Les conditions
Description détaillée
ABSTRACT INTRODUCTION: Children are regarded as the precious gift in world. It is estimated that between 8% and 12% of couples worldwide suffer from infertility with rate of 10% in India and about 20 million children are orphan even then adoption rates are falling in India.
OBJECTIVES: To assess and compare the knowledge score and opinion score regarding adoption among adults of different age groups.To determine relationship between knowledge and opinion regarding adoption among adults.To seek association of knowledge score and opinion score regarding adoption with selected variables.
METHODOLOGY: A descriptive cross sectional survey design was used. 400 adults of rural (200) and urban (200) area were selected by using quota sampling technique. The data was collected by structured knowledge questionnaire and structured likert scale.
Type d'étude
Inscription (Réel)
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
The population of the present study was Adults residing in rural and urban area of Haryana.
Target population:- Adults residing in rural areas and urban areas of Ambala District Haryana.
Accessible population:- Adults residing in rural area (Mullana) and urban area (muncipal corporator ward number 14 and ward number 15 of Mahesh Nagar) of Ambala District Haryana and available during data collection.
La description
Inclusion Criteria:
- Adults who were able to understand Hindi and English.
- Who were willing to participate in the study.
Exclusion Criteria:
- Adults who were not available at the time of data collection.
- Adults having any psychological impairment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
|---|
|
Early young adult (20 years - 30 years)
Adults who were in the age group of 20 - 30 years was the first group.
There were made two separate same age group one for rural and one for urban areas adults.
Each areas age group consist 50 adults of 20-30 years.
|
|
Middle age adult (31 -50 years)
Adults who were in the age group of 31-50 years were in second group.
There were made two separate same age group one for rural and one for urban areas adults.
Each areas age group consist 50 adults of 31-50 years.
|
|
Late adult (51 years - 65 years)
Adults who were in the age group of 51-65 years were in third group.
There were made two separate same age group one for rural and one for urban areas adults.
Each areas age group consist 50 adults of 51-65 years.
|
|
>65 years
Adults who were in the age group of >65 years were in fourth group.
There were made two separate same age group one for rural and one for urban areas adults.
Each areas age group consist 50 adults of >65 years.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Structured Questionnaire
Délai: 25-30 minutes
|
One time assessment of knowledge of adults regarding adoption.
Total score is calculated by finding the sum of the correct answer.
Each correct answer scored as 1 and each incorrect answer scored as 0. It consists scale of scores 23-30 = Very Good, 19-22 = Good, 15-18 = Average, 0-14 = Below Average
|
25-30 minutes
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Likert Scale
Délai: 18-20 minutes
|
3 point Likert Scale was used to assess opinion of adults regarding adoption.
Total score is calculated by finding the sum of the 30 items. it consist 15 positive statements and 15 negative statements.
Each positive statement scored as 3= agree, 2= uncertain,1=disagree and each negative statement scored as 3=disagree, 2=uncertain, 1= agree.
it consists the scale of scores 68-90:Favourable 45-67: Moderately Favourable, 30-44: Unfavourable
|
18-20 minutes
|
Collaborateurs et enquêteurs
Les enquêteurs
- Directeur d'études: Poonam Sheoran, Ph.D Nursing, Maharishi Markandeshwar University
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
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
Autres numéros d'identification d'étude
- 100015
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
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
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
Essais cliniques sur Connaissance
-
Andrzej Frycz Modrzewski Krakow UniversityRecrutementÉtouffer chez les nourrissons | Réanimation cardiopulmonaire (RCR) | Formation des premiers secours | Knowledg parentalPologne