The Impact of Background Music in Reducing Stress in Preclinical Dental Labs

October 30, 2018 updated by: sudhir rama varma, Ajman University
This study was designed to evaluate students' level of stress and impact of background music on their efficiency of work, performance and learning ability during pre-clinical lab.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The reported high level of stress among dental students and its consequences, considering the known benefits of background music. This study was designed to evaluate students' level of stress and impact of background music on their efficiency of work, performance and learning ability during pre-clinical lab.

METHODOLOGY: In this cross-sectional questionnaire study, 61 preclinical students from the college of dentistry, Ajman university-Fujairah campus who met the defined inclusion criteria participated.

After a semester of the normal lab without BM (Background Music), various genres of BM were introduced in the lab. Psychological stress assessment was done using P.S.S (Perceived Stress Scale).Students were asked to fill up a written feedback questionnaire at the end of six weeks of BM. Descriptive statistics and Chi-square test were used in order to study the statistical relationships among groups.

Study Type

Observational

Enrollment (Actual)

60

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 to 23 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The study population were both male and female students aged between 18-23 yrs who were students of Ajman University dental campus,they are attending preclinical dental labs and belong to the 2nd and third year of the dentistry program

Description

Inclusion Criteria:

  • Students were not taking any
  • medication for anxiety
  • did not suffer from depression
  • did not have any systemic illness;
  • and they had no aversion towards music.

Exclusion Criteria:

  • Students who were taking
  • medication for anxiety
  • had depression
  • had systemic illness
  • they had aversion towards music

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
Intervention / Treatment
Active
Evaluate stress among dental students by Questionnaire

students were involved in the pre-clinical prosthodontic lab. Participation in these labs were mandatory and it involved crown and bridge preparations on typodont models. There were 2 sessions of these labs per week, one for each gender. Each session lasted for 3 hours.

The study was conducted in 2 phases. At the beginning of the first phase of the study, the labs were conducted without any BM for 4 weeks. PSS(perceived stress scale), a standardized and validated, self-reporting international test was used for measuring the level of psychological stress were administered to all participants.

the present level of stress, comfort zone & coping with stress
Evaluate how stress was coped, the coping mechanisms used through Questionnaire

students were involved in the pre-clinical prosthodontic lab. Participation in these labs were mandatory and it involved crown and bridge preparations on typodont models. There were 2 sessions of these labs per week, one for each gender. Each session lasted for 3 hours.

The study was conducted in 2 phases. At the beginning of the first phase of the study, the labs were conducted without any BM for 4 weeks. PSS(perceived stress scale), a standardized and validated, self-reporting international test was used for measuring the level of psychological stress were administered to all participants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
coping mechanisms practiced by pre-clinical dental students to cope up stress.
Time Frame: From baseline to 5 months
How students cope with the stress they experience by answering a questionnaire
From baseline to 5 months
PSS ((perceived stress scale) internationally used psychological scale for measuring the level of stress, it measures how stressful are the situations in one's life.)
Time Frame: From baseline to 5 months
It consist of ten questions, each question has five answers arranged from zero to four. Each number has a point which reveals the level of stress for each question. Points were calculated according to the calculation system of the scale.
From baseline to 5 months
PSS scale range from 0-4,with 0-no stress,1-mild stress,3-moderate stress and 4-severe stress
Time Frame: From baseline to 5 months
The students were graded on their response to the questionnaire
From baseline to 5 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feedback of music of male and female pre-clinical dental students.
Time Frame: From baseline to 5 months
What type of music students feel more relaxed while working in dental labs by answering certain questions in the form of questionnaire
From baseline to 5 months
PSS scale range from 0-4,with 0-no stress,1-mild stress,3-moderate stress and 4-severe
Time Frame: From Baseline to 5 months

What type of music students feel more relaxed while working in dental labs by asking certain questions in a questionnaire

a measurement tool in the form of questionnaire

From Baseline to 5 months

Collaborators and Investigators

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

February 24, 2016

Primary Completion (Actual)

July 25, 2016

Study Completion (Actual)

August 20, 2016

Study Registration Dates

First Submitted

October 10, 2018

First Submitted That Met QC Criteria

October 30, 2018

First Posted (Actual)

October 31, 2018

Study Record Updates

Last Update Posted (Actual)

October 31, 2018

Last Update Submitted That Met QC Criteria

October 30, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • RDF-2015/16-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Results of the study,also methodology

IPD Sharing Time Frame

2 months

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

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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