Assessment of Knowledge, Attitude and Practice of Eligible Couples Regarding Eugenics

August 1, 2017 updated by: Hem Sadhanu, Maharishi Markendeswar University (Deemed to be University)

A Descriptive Comparative Study to Assess Knowledge, Attitude and Practice Regarding Eugenics Among Eligible Couples of Selected Area of Ambala, Haryana (India)

A Descriptive study to assess the knowledge, attitude and practice regarding eugenics among eligible couples of selected area of Ambala, Haryana, India. Eligible couples were the married couples where wife is in the age group of 15-45 years planning for conception, have conceived and may or may not have any living child.Eugenics are to methods that are adopted by eligible couples for having physically and psychologically healthy conception and pregnancy.

Study Overview

Status

Completed

Detailed Description

To assess the knowledge, attitude and practice the structured knowledge questionnaire, attitude 5-point likert scale and expressed checklist tool were prepared. A sample size of 318 was calculated by power analysis and eligible couples were selected by Purposive sampling technique from rural and urban area of Ambala Haryana, India.

Each eligible couples (separately husband and wife) data was collected through Self- Report technique.one time assessment only done.

Study Type

Observational

Enrollment (Actual)

318

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 45 years (ADULT, CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Eligible couples of rural and urban areas of Ambala Haryana, India

Description

Inclusion Criteria:

  • who were present at the time of data collection
  • who were willing to participate in the study
  • who can read and write English/Hindi

Exclusion Criteria:

  • who have more than 2 children
  • who had undergone permanent sterilization

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
eligible couples
Eligible couples refers to methods that are adopted by eligible couples for having physically and psychologically healthy conception and pregnancy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Structured Questionnaire
Time Frame: 15-20 min

It consisted of 34 knowledge items to assess the knowledge of Eligible couples regarding Eugenics. The following content areas were:

  • Concept of Eugenics
  • Screening of Disease
  • Nutrition
  • Vaccination
  • Lifestyle
  • Exposure to substance abuse or toxins All 34 test items were multiple choice questions. Each item had a single correct answer. Every correct answer was awarded a score of '1' and every incorrect answer was assigned a score of 00. The maximum possible score was 34 and minimum score was 00 on the structured knowledge questionnaire . Higher score indicated that eligible couples have good knowledge regarding Eugenics. Based on scoring criteria on Structured Knowledge Questionnaire, knowledge was categorized into four level of knowledge.Excellent (27-34),Good (21-26),Average (17-20),Below average(0-16)
15-20 min

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Structured Attitude 5-point likert Scale
Time Frame: 10-15 min

Scale consisted of 30 items on which the respondent had to respond on 5- points Likert's scale.Each statement score was divided as strongly agree, agree, undecided, disagree, strongly disagree (maximum score was 150 and minimum score was 30).Tool had 15 positive items and 15 negative items.Positive statements were scored SA (Strongly Agree) -5, A (Agree)-4, U (Undecided)-3, D (Disagree)-2, SD (Strongly Disagree)-1. Negative statements were scored SA (Strongly Agree) -1, A (Agree)-2, U (Undecided)-3, D (Disagree)-4, SD (Strongly Disagree)-5.

Based on scoring criteria on Structured Attitude Scale, Husbands and Wives attitude was categorized into three level of Attitude Favourable (225-300), Moderately Favourable(180-224),Unfavourable(60-179)

10-15 min
Expressed Husband Checklist
Time Frame: 7-8min
Structured expressed practice checklist was developed to assess expressed practices of Husbands regarding Eugenics. Checklist consists of 18 items. These items designed to elicit information on practices of Husbands regarding Traditional and Non-traditional. Each item was provided with 2 responses Yes(Y) and No (N) and was scored as 1 and 0 respectively.
7-8min
Expressed Wife Checklist
Time Frame: 10-12min
Structured expressed practice checklist was developed to assess expressed practices of wives regarding Eugenics. Checklist consists of 32 items. These items designed to elicit information on practices of wives regarding Traditional and Non-traditional. Each item was provided with two responses Yes(Y) and No (N) and was scored as 1 and 0 respectively
10-12min

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Dr. Poonam Sheoran, Ph.d Nursing, M.M.University, Mullana, Ambala Haryana, India

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

November 1, 2015

Primary Completion (ACTUAL)

January 1, 2017

Study Completion (ACTUAL)

June 1, 2017

Study Registration Dates

First Submitted

July 30, 2017

First Submitted That Met QC Criteria

August 1, 2017

First Posted (ACTUAL)

August 2, 2017

Study Record Updates

Last Update Posted (ACTUAL)

August 2, 2017

Last Update Submitted That Met QC Criteria

August 1, 2017

Last Verified

July 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 781

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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