Evaluation of the Efficiency of the Chronic Pain Management Training Program

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

66 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-16

Study Completion Date

2022-06-13

Brief Summary

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The research will be conducted to evaluate the effectiveness of the web-based chronic pain management training program developed for nursing students. It is planned in a randomized controlled triple-blind design with the final year nursing students of the Nursing Department of Çankırı Karatekin University in a pre-test-post-test order.

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Detailed Description

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Conditions

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Nursing Caries Chronic Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomization: After applying the exclusion criteria to a total of 94 students, the students who accepted to participate in the study was randomly selected into two groups (A and B) of 35 students by simple random sampling by creating a computer-assisted simple random numbers table (www.randomizer.org). Selected students was randomly assigned so that the general academic achievement grades of both groups were homogeneous. The groups was randomly assigned to the intervention or control group by the code "A" and "B" by the software specialist.

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

It was explained to all students that training was given over the website https://www.agriegitimi.net and the starting time of the training was announced on the website. Students were told that they were be able to attend training and testing at the relevant time according to notifications. Students were not know that they were in the experimental or control group. In this way, students were blinded. Only the software specialist could know the students in the intervention and control groups. The data could sent to the statistician by the software specialist as group A and B data. This way the statistician could be blind. The researcher could not present at any stage of data collection. After the statistical analysis was done and the research report was written, the coding of the experimental and control groups were explained to the researcher by the software specialist.

Study Groups

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Control group

The students in the control group will be given a pre-test, and two weeks later, the post-test will be applied. After the chronic pain education group completes the research, the chronic pain education program will be opened to the students in the control group, too.

Group Type SHAM_COMPARATOR

No intervention

Intervention Type OTHER

No intervention will be made.

Chronic pain education group

The pre-test will be opened to the students in the chronic pain education group simultaneously with the opening of the post-tests for the control group.After the students in the chronic pain education group completed the pre-test, the chronic pain management training program developed for nursing students will be applied for 2 weeks. Post test will be applied at the end of all training videos and evaluation questions.

Group Type EXPERIMENTAL

chronic pain management education program

Intervention Type OTHER

The chronic pain management training program will be applied for 2 weeks. The training consists of 15 videos about theory and practice topics in chronic pain management. There are evaluation questions at the end of each video.

Interventions

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chronic pain management education program

The chronic pain management training program will be applied for 2 weeks. The training consists of 15 videos about theory and practice topics in chronic pain management. There are evaluation questions at the end of each video.

Intervention Type OTHER

No intervention

No intervention will be made.

Intervention Type OTHER

Other Intervention Names

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Experimental group Control group

Eligibility Criteria

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Inclusion Criteria

* Nursing Grade 4
* with internet access
* Students who volunteered to participate in the research

Exclusion Criteria

* Having a diagnosed psychiatric disorder
* Difficulty in understanding and speaking Turkish
* Graduated from Health Vocational High School
* Attending any training on pain and/or having a pain education certificate

Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes