Home » Trials » SLCTR/2013/028


A controlled trial on the effectiveness of an educational intervention to improve the quality of medical record documentation among medical officers in a district of Sri Lanka

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SLCTR Registration Number

SLCTR/2013/028


Date of Registration

17 Sep 2013

The date of last modification

Mar 03, 2019


Trial Status



Application Summary


Scientific Title of Trial

A controlled trial on the effectiveness of an educational intervention to improve the quality of medical record documentation among medical officers in a district of Sri Lanka


Public Title of Trial

A study on the effectiveness of an education programme to improve medical record documentation


Disease or Health Condition(s) Studied

Medical record documentation


Scientific Acronym

None


Public Acronym

None


Brief title

None


Universal Trial Number

None


Any other number(s) assigned to the trial and issuing authority

EC-12-002 (Ethics Review Committee of the Faculty of Medicine, Colombo)


Trial Details


What is the research question being addressed?

What is the effect of an educational intervention on the medical record documentation by medical officers?


Type of study

Interventional


Study design

Allocation

Non-randomized controlled trial


Masking

Masking not used


Control

Standard therapy/practice


Assignment

Parallel


Purpose

Health services research


Study Phase

Not Available


Intervention(s) planned

Medical officers in five selected hospitals of Kalutara district will form the intervention group and medical officers from five selected hospitals in the Matara district will form the control group.

The intervention group will receive a guide book on correct documentation of medical records. They will also be invited to participate in a 2 hour lecture discussion on medical record documentation.

The control group will not receive any intervention.


Inclusion criteria

All the medical officers working in the selected hospitals (including intern medical officers)


Exclusion criteria

Medical officers who are posted to the selected hospitals after the commencement of the study



Primary outcome(s)

1.

Change in the quality of medical record documentation by the doctors in inpatient medical records (using the validated Physician Documentation Quality Assessment Tool - PDQI)

[

At baseline, 12 weeks and 18 weeks

]
2.

Change in knowledge regarding medical record documentation (using a self administered questionnaire)

[

At baseline, 12 weeks and 18 weeks

]

Secondary outcome(s)

1.

Change in the quality of documentation of the final diagnosis (using PDQI)

[

At baseline, 12 weeks and 18 weeks

]

Target number/sample size

270 medical officers from Kalutara district and 217 medical officers from Matara district


Countries of recruitment

Sri Lanka


Anticipated start date

2013-09-17


Anticipated end date

2014-03-31


Date of first enrollment


Date of study completion


Recruitment status

Pending


Funding source

None


Regulatory approvals



State of Ethics Review Approval


Status

Approved


Date of Approval

2012-01-12


Approval number

EC-12-002


Details of Ethics Review Committee

Name: Ethics Review Committee, Faculty of Medicine, University of Colombo
Institutional Address:No. 25, Kynsey Road, Colombo 00800 Sri Lanka
Telephone:+94-11-2695300 (Extension: 240)
Email: ethicscommitteemfc@gmail.com

Contact & Sponsor Information


Contact person for Scientific Queries/Principal Investigator

Dr. Nandalal Mahendra Wijesekera
Registrar in Community Medicine
National Institute of Health Sciences, Kalutara

0777908709

nmwijesekera@yahoo.com

Contact Person for Public Queries

Dr. Nalika Gunawardena
Senior Lecturer in Community Medicine
Department of Community Medicine, Faculty of Medicine, Colombo

077 6975402

nalikaguna@hotmail.com, nalikaguna@yahoo.com


Primary study sponsor/organization

National institute of Health Sciences

Nagoda, Kalutara
034 - 2222264
034 - 2226319

http://www.nihs.gov.lk/

Secondary study sponsor (If any)

None





Trial Completion details


Do the investigators plan to share identified individual clinical trial participant-level data (IPD)?


IPD sharing plan description


Study protocol available


Protocol version and date

Not Available


Protocol URL

Not Available


Results summary available

No


Date of posting results


Date of study completion


Final sample size


Date of first publication


Link to results


Brief summary of results