- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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"
Study Overview
Status
Conditions
Detailed Description
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.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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.
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.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Structured Questionnaire
Time Frame: 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
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Likert Scale
Time Frame: 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
|
Collaborators and Investigators
Investigators
- Study Director: Poonam Sheoran, Ph.D Nursing, Maharishi Markandeshwar University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 100015
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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