The Effect of Bedside Whiteboard Use on Anxiety, Depression and Nursing Care in Chronic Obstructive Pulmonary Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAgri Ibrahim Cecen University

About this trial

ABSTRACT Chronic obstructive pulmonary disease (COPD) is a disease characterized by the inability of the body to adequately exchange gases, resulting in progressive shortness of breath that can form secretions and compromise the performance of daily activities. COPD is reported as the third most common cause of death worldwide, with 3.23 million deaths in 2019. Anxiety and depression are common in individuals with COPD. However, COPD is more common in patients with other chronic diseases such as hypertension, diabetes, cancer or musculoskeletal disorders. Communication is a key component in interprofessional care as well as in improving patient care outcomes. Strategies to address gaps in the quality of information and communication between patients, caregivers and professionals improve patient safety as well as quality of care. One of these strategies is the use of whiteboards at the bedside. The use of whiteboards at the bedside has emerged as a strategy to improve interprofessional team participation, communication and information sharing with care teams, patients and families. This study will be conducted in randomized controlled single blind parallel groups to examine the effect of bedside whiteboard use on anxiety, depression and nursing care satisfaction in COPD patients. The research will consist of patients who are hospitalized in Atatürk University Research Hospital Chest Diseases Clinic and who meet the inclusion criteria. In the results of the research, it is thought that the use of whiteboard will affect the communication between health care team members.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18 years of age or older

Having a medical diagnosis of COPD

To be in a condition to be followed up with at least 7 days

Disqualifiers

- Having strong reading and comprehension skills

Trial design

Design model

Parallel

Treatments tested in this trial

  • use of whiteboard

    Other intervention

    Patients will be followed up for 7 days. Routine nursing care will be applied to the control group. The following information will be included on the whiteboard fixed in the patient room for the intervention group. * Nurse's name * Doctor's name * Treatment times during the day * Nursing interventions and hours for the diagnoses considered for the patient's major problems * Timing of diagnostic and imaging techniques to be performed on the patient * Content of appropriate discharge education for the patient * Points to be considered by the patient before and after treatment * Dietary considerations for the patient * Nurse and patient's private note As a result of the data obtained, statistical analyses will be performed and interpreted to determine the effect of whiteboard use on anxiety, depression and satisfaction with nursing care in COPD patients.

Treatment groups

128 Participants
are divided into 2 treatment groups
Group A: Whiteboard groupExperimental treatment 1 intervention
Group B: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

How does the use of whiteboard affect anxiety, depression and nursing care satisfaction in COPD patients?

The Hospital Anxiety and Depression Scale will be used to examine the effect of the whiteboard to be used for COPD patients on anxiety and depression. A total scale score of 28 and above indicates a high level of anxiety and depression.

Time frame
From registration until the end of the 3th month
2

How does the use of whiteboard affect anxiety, depression and nursing care satisfaction in COPD patients?

The Patient Satisfaction with Nursing Care Quality Questionnaire Scale will be used to examine the effect of the whiteboard to be used for COPD patients on nursing satisfaction. A total score of 47.5 and above indicates high nursing care satisfaction.

Time frame
From registration until the end of the 3th month

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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