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The Effect of Training Given to Nurses Caring for Dying Cancer Patients and Their Families on Care and Difficulties

Ç

Çukurova University

Status

Completed

Conditions

Dying Patient
Nursing Caries

Treatments

Other: Education

Study type

Interventional

Funder types

Other

Identifiers

NCT05775926
05.04.2019/87

Details and patient eligibility

About

Nursing is a profession that is human and is based on nursing care. Humans are social creatures that need care from the moment they are born.Today's scientific developments and changing technology have affected the health system.Many dying patients want to be hospitalized in order to receive better care and treatment. Depending on this situation, the frequency of nurses giving care to dying patients and their families has increased in hospitals. In order to increase the quality of the care given to the dying patient and his family and to reduce the difficulties experienced while giving this care, the nurse who provides the care should have sufficient knowledge and skills about the care of the dying patient and his family.

This research will be conducted as a randomized controlled experimental study in order to determine the effect of education on the nursing care given and the difficulties experienced by the nurses who care for the dying cancer patients and their families.

Full description

The research was carried out to determine the effect of the training given to the nurses who care for the dying cancer patients and their families, on the nursing care and the difficulties experienced.

H1: There is a significant difference between the "Nursing Care Scale for Dying Patients and Their Families" pre- and post-test scores of the intervention and control groups.

H2: There is a significant difference between the pre-test and post-test scores of the "Nurse Difficulty Scale for Dying Patients and Their Families" of the intervention and control groups.

Enrollment

52 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volunteer
  • Working in a clinic where adult cancer patients are hospitalized for at least 1 year

Exclusion criteria

  • On leave
  • Not volunteering

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

52 participants in 2 patient groups

Experimental
Experimental group
Description:
Experimental Group: Nurses who met the criteria for participating in the study were informed about the study and their consent was obtained. Data collection forms were collected by the researcher at the end of the working hours. Training groups were formed on the days and times determined according to the interviews with the clinics where the research was conducted. In each hospital, training groups were formed outside the working hours of the nurses. The training was given to the nurses in the intervention group in an environment suitable for training in two days and 4 modules using interactive teaching methods. After the training, a month was waited for the nurses in the intervention group to experience care. One month after the training was given, data collection forms were distributed to the nurses in the intervention group and asked to fill in according to their self-reports.
Treatment:
Other: Education
Control
No Intervention group
Description:
Control Group: Nurses who met the criteria for participating in the study were informed about the study and their consent was obtained. Data collection forms were collected by the researcher at the end of the working hours. No training was given to the control group. However, after the post-test application was made to the control group, the same training was given to the experimental group. One month later, data collection forms were distributed to the nurses in the control group and they were asked to fill in according to their self-reports. Data collection forms were collected by the researcher at the end of the working hours. Filling in the data takes about 15 minutes.

Trial contacts and locations

1

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Central trial contact

Meltem Akbaş, PhD

Data sourced from clinicaltrials.gov

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