Knowledge and Perceptions Regarding JSSK and RBSK in Patients and Nurses: A Comparative Study

June 29, 2016 updated by: DR. VIKRAM DATTA, Lady Hardinge Medical College

Knowledge and Perceptions Regarding Janani Shishu Suraksha Karyakram (JSSK) and Rashtriya Bal Swasthya Karyakram (RBSK) Programs in the Patients/Patient Attendants,Nursing Students and in Service Nurses: A Comparative Study

Observational, cross sectional study, carried out with the help of a pre-designed and pre-tested questionnaire with the research hypothesis as: Knowledge and perception regarding JSSK and RBSK in nursing students is better as compared to in-service nurses as well as patients/patient attendants (attending LHMC and associated hospitals, New Delhi, India)

Study Overview

Status

Completed

Conditions

Detailed Description

The objectives of the study were to:

  1. To study knowledge and perceptions regarding JSSK and RBSK programs in the patients/patient attendants, nursing students and in-service nurses attending LHMC and associated hospitals.
  2. To compare knowledge and perceptions regarding JSSK and RBSK programs in the patients/patient attendants, nursing students and in-service nurses attending LHMC and associated hospitals.
  3. To identify factors contributing to knowledge regarding JSSK and RBSK programs in the patients/patient attendants, nursing students and in-service nurses attending LHMC and associated hospitals.

Study Type

Observational

Enrollment (Actual)

293

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

100 participants enrolled from the patients/attendant subset,93 Nursing students(final year) and interns from the Nursing college, LHMC along with 100 nurses posted in the LHMC and associated hospitals enrolled in the study.

Description

Inclusion Criteria:

Group 1) Patients/Attendants:

  • All study subjects must be female.
  • Age more than 18 years.
  • Written informed consent to participate in the study.

Group 2) Nursing Student:

  • Students / intern at College of nursing LHMC pursuing Bsc Nursing
  • Written informed consent to participate in the study

Group 3) In-service Nurses:

  • Posted in Department of Paediatrics indoor/OPD/well-baby clinics/immunisation clinics or Department of Gynaecology and Obstetrics indoor/OPD/emergency/Ante-natal clinics/Post-natal clinics of Lady Hardinge Medical College and associated hospitals.
  • Written informed consent to participate in the study

Exclusion Criteria:

  • Males for the patient/attendant group 1

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

  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Patient/patient attendants
  1. Study subjects will be females.
  2. Age at enrolment should be more than 18 years.
  3. Attending Department of Paediatrics OPD/emergency/well-baby clinics/immunisation clinics OR Department of Gynaecology and Obstetrics OPD/emergency/Ante-natal clinics/Post-natal clinics of Lady Hardinge Medical College and associated hospitals.
  4. Written informed consent to participate in the study.
Students,nursing
  1. Pursuing Bsc Nursing(in their final year) or intern of college of nursing LHMC
  2. Written informed consent to participate in the study
In-service nurses
  1. Posted in Department of Paediatrics indoor/OPD/well-baby clinics/immunisation clinics or Department of Gynaecology and Obstetrics indoor/OPD/emergency/Ante-natal clinics/Post-natal clinics of Lady Hardinge Medical College and associated hospitals.
  2. Written informed consent to participate in the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge and perception regarding JSSK and RBSK in study population groups
Time Frame: 90 days
The knowledge and perception will be evaluated by yes, no responses using predesigned and pretested questionnaire presented to each of the three study groups.
90 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of the knowledge and perception regarding JSSK and RBSK in study population groups
Time Frame: 90 days
The knowledge and perception will be compared using yes and no responses obtained on predesigned and pretested questionnaire presented to each of the three study groups.
90 days
Study of factors contributing to knowledge regarding JSSK and RBSK in study population groups
Time Frame: 90 days
The factors will be identified and evaluated using yes and no responses obtained on the predesigned and pretested questionnaire presented to each of the three study groups.
90 days

Collaborators and Investigators

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

Sponsor

Lady Hardinge Medical College

Investigators

  • Study Chair: Vikram Datta, MD,DNB, Lady Hardinge Medical College,New Delhi,India

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

June 1, 2015

Primary Completion (Actual)

June 1, 2016

Study Completion (Actual)

June 1, 2016

Study Registration Dates

First Submitted

June 24, 2016

First Submitted That Met QC Criteria

June 29, 2016

First Posted (Estimate)

June 30, 2016

Study Record Updates

Last Update Posted (Estimate)

June 30, 2016

Last Update Submitted That Met QC Criteria

June 29, 2016

Last Verified

June 1, 2016

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • LadyHardingeMC

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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