Individualized Care Perceptions of Patients Receiving Outpatient Chemotherapy: A Qualitative Study
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Yalova
About this trial
The purpose of this observational study is to learn how people receiving chemotherapy in a clinic without staying overnight (outpatient) feel about the care they receive. The study focuses on individualized care, which means nursing care that is tailored specifically to each person's unique needs, values, and lifestyle.
Background:
Cancer treatment often involves chemotherapy (medicine used to kill cancer cells). While these treatments help fight the disease, they can also cause side effects like nausea or tiredness, which affect daily life. Nurses play a key role in helping people manage these effects. This research aims to understand how "individualized care" helps participants feel valued and supported during their treatment journey.
The study aims to answer these key questions:
How do participants describe their experiences with nursing care?
What are the specific needs and expectations of these individuals for care that feels personal to them?
How does personalized care affect their ability to manage symptoms and follow their treatment plan?
Scope and Setting:
This study will take place at the Yalova Training and Research Hospital within the Outpatient Chemotherapy Unit. The research will be conducted between May 1, 2026, and April 1, 2027.
Method and Participants:
The researchers plan to interview 10 to 20 participants who are over 18 years old and receiving treatment at the clinic. The final number of participants will be decided when the researchers find that no new information or themes are being discovered in the interviews (a stage called "data saturation").
Participants will:
Take part in a private, one-on-one interview with a researcher.
Answer open-ended questions about their thoughts and feelings regarding their nursing care.
Allow the interview to be voice-recorded to ensure all information is captured accurately.
Spend approximately 30 to 45 minutes sharing their personal experiences.
Privacy and Ethics:
Participant privacy is a top priority. All personal information and voice recordings will be kept strictly confidential. In the final report, fake names (aliases) will be used so that no one can be identified. Participants can choose to leave the study at any time. The study follows international ethical rules to protect the rights of every participant.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Continuing treatment at the Outpatient Chemotherapy Unit of the relevant hospital.
Voluntarily agreeing to participate in the study.
Being over 18 years of age.
Being proficient in Turkish.
Disqualifiers
Not receiving ongoing treatment at the Outpatient Chemotherapy Unit of the relevant hospital.
Declining to participate in the study voluntarily.
Unwillingness to answer questions or lack of cooperation during the interview.
Trial population
Patients receiving ongoing treatment at the Outpatient Chemotherapy Unit of Yalova Training and Research Hospital
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Number of participants expressing specific themes regarding perceptions of individualized nursing care.
This outcome measures the frequency and depth of perceptions of individualized nursing care as shared by participants during semi-structured interviews. Data will be analyzed using descriptive and thematic analysis. The results will be reported as the identified themes and the number of participants who expressed each specific theme or perception.
Time frame
Through study completion (approximately 12 months).Secondary outcomes
1
Number of participants identifying specific categories of individualized nursing care needs and expectations.
Through semi-structured interviews, participants will describe their specific nursing care needs and expectations. Data will be analyzed to identify common categories of needs. Results will be reported as a list of identified care need categories and the number of participants who expressed each specific need or expectation.
Time frame
Through study completion (approximately 12 months).Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: