The Effects of "Workplace Health Promotion Program" on Pain, Fatigue, Stress in Nurses

NCT ID: NCT03908554

Last Updated: 2019-04-16

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

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-04-03

Study Completion Date

2018-12-10

Brief Summary

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Pain, fatigue, and stress lead to decrease on their work performance with biopsychosocial functioning disorders on nurses. This study was conducted to examine the effects of the "Workplace Health Promotion Program" (WHPP) on pain, fatigue, stress, professional quality of life (Pro-QoL) and coping skills for nurses.

Detailed Description

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The investigators conducted a randomized control trail in 30 nurses admitted to their Hospital. Progressive relaxation training, posture and breath exercises and ergonomic suggestion as a WHPP was applied to the intervention group (n=15) during the five weeks. Visual Analogue Scale (VAS) was used to determine the pain, fatigue and stress levels of the nurses. Brief COPE and the Professional Quality of Life Scale, Version 4 (Pro-QoL) were used to evaluate the coping skills and quality of life. The evaluations were performed three times on all the participants as; before and after training and the one-year follow-up.

Inclusion criteria of this study were working actively and at least 40 hours working in a week. Participants who have psychiatric illnesses with or without medication, prior training or current use of relaxation therapy and participants without consent were excluded.

Eighty nurses aged between 18 and 65, working in a hospital have been informed about the study. Forty-three nurses who met the criteria and signed consent forms were included in this study. WHPP was PMR training, posture and breath exercises, and ergonomic suggestions.

Conditions

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Nurses Work-Related Stress Disorder Pain Fatigue

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The WHPP was applied to the intervention group in the workplace for two times a week for five weeks. During the first 5 minutes of the session, breathing exercises, 20 minutes, PMR and 10 minutes, posture exercises were performed. PMR has progressed gradually to every session. The program is under control with a follow-up chart of what the participants do every day, and the participants were supported with various reminders (i.e., graphical leaflets on PMR techniques which also can be used as a guide while practicing at home). Participants of the control group rested in a room for 40 minutes and were told that they could read every session.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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intervention

The WHPP was applied to the intervention group in the workplace for two times a week for five weeks. During the first 5 minutes of the session, breathing exercises, 20 minutes, PMR and 10 minutes, posture exercises were performed. PMR has progressed gradually to every session. The program is under control with a follow-up chart of what the participants do every day, and the participants were supported with various reminders (i.e., graphical leaflets on PMR techniques which also can be used as a guide while practicing at home).

Group Type EXPERIMENTAL

WORKPLACE HEALTH PROMOTION PROGRAM

Intervention Type OTHER

WHPP was PMR training, posture and breath exercises, and ergonomic suggestions.

Control

Participants of the control group rested in a room for 40 minutes and were told that they could read every session.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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WORKPLACE HEALTH PROMOTION PROGRAM

WHPP was PMR training, posture and breath exercises, and ergonomic suggestions.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Working actively and at least 40 hours working in a week,
* Working as a nurse.

Exclusion Criteria

* Have psychiatric illnesses with or without medication,
* Have prior training or current use of relaxation therapy and participants without consent.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Hacettepe University

OTHER

Sponsor Role lead

Responsible Party

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Gokcen Akyurek

PhD PT, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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431-1271

Identifier Type: -

Identifier Source: org_study_id

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