Caregiver, Caregiver Burden of Caregivers, Palliative Care, PEG Training, Quality of Life of Caregivers
Conditions
Keywords
Palliative care, Nutrition, PEG, Caregiver, caregiver burden, Quality of life, PEG training
Brief summary
The study was planned to evaluate the effects of discharge training on PEG use given to palliative care patients' relatives on the caregiver burden and quality of life of the relatives. The main questions that the study aims to answer are as follows: * How does PEG training given before discharge affect the knowledge level of caregivers on PEG use? * How does PEG training given before discharge affect the caregiver burden? * How does PEG training given before discharge affect the caregiver's caregiver stress? * How does PEG training given before discharge affect the quality of life of the caregivers? The researchers will compare the PEG training given before discharge with a control group that did not receive training in this regard in order to evaluate the effects of PEG training given before discharge on the caregiver burden, caregiver stress and quality of life of the caregivers. The study will use a general information form, the Caregiver Burden Scale, the Caregiver Stress Index Form, the SF 36 Quality of Life Scale, and the Percutaneous Endoscopic Gastrostomy Tube Nutrition Information Scale for Caregivers. Participants: * Face-to-face interviews will be conducted with caregivers at 0, 1, and 3 months. * The forms used in the study will be filled out at each interview. * The intervention group will be trained only at the first interview.
Interventions
BEHAVIORALPEG training
The caregivers will be given a general information form, the Caregiver Burden Scale, the Caregiver Stress Index Form, the SF 36 Quality of Life Scale, and the Caregiver Knowledge Scale for Nutrition with Percutaneous Endoscopic Gastrostomy Tube at each meeting (0, 1, and 3 months.). The intervention group will be trained on PEG use before discharge at the first interview.
OTHERControl
The caregivers will be given a general information form, the Caregiver Burden Scale, the Caregiver Stress Index Form, the SF 36 Quality of Life Scale, and the Caregiver Knowledge Scale for Nutrition with Percutaneous Endoscopic Gastrostomy Tube at each meeting (0.,1. ve 3. monts).
Sponsors
Uludag University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)
Intervention model description
Quasi-experimental
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* The caregiver must be over 18 years old * The caregiver must be willing and able to participate in the study * The caregiver must be primarily responsible for the patient's care * The patient they are caring for must be receiving palliative care * The patient they are caring for must be receiving PEG feeding * The patient they are caring for must be over 18 years old * The patient they are caring for must have been diagnosed with stroke at least six months ago * The caregiver must have a mini mental test score of 25 points or more * The Beck depression scale score must be under 17 points * The caregiver must have a score of over 16 points on the Readiness to Provide Care Scale
Exclusion criteria
* The caregiver is under the age of 18 * The caregiver is not willing and able to participate in the research * The caregiver has a physical disability or serious health problem that makes it difficult to provide care * The patient they are caring for is under the age of 18 * The patient they are caring for has been diagnosed with cancer, endocrine system or GI disease * The caregiver has a mini mental test score of less than 25 * The Beck depression scale score is 17 points or higher * The caregiver has scored 16 or lower on the Readiness to Provide Care Scale * The caregiver has communication problems * The caregiver has been diagnosed with depression or psychiatric disorder * The caregiver is receiving psychotherapy/psychological support * The caregiver is taking antidepressants and/or anxiolytics * The caregiver has sensory loss related to vision and hearing
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Caregiver burden level of caregivers | 0th month (1st day), 1st month and 3rd month | The Caregiver Burden Scale: The scale is scored from 0 to 88. A higher score indicates a higher level of distress. |
| The quality of life level of the caregivers | 0th month (1st day), 1st month and 3rd month | Short Form 36- Quality of Life Scale: The scale is scored from 0 to 100. A high score indicates good health. |
Countries
Turkey (Türkiye)
Contacts
CONTACTHicran Yıldız
PRINCIPAL_INVESTIGATORHicran Yıldız, Prof.Dr.
Bursa Uludag Unversity
Outcome results
None listed