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Recruiting NCT06723600

Effect of Informing Family Members of Patients During Surgery

No phase Interventional Anxiety

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Information.
Who it may be relevant to
Registry conditions: Anxiety. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Informing Family Members of Patients by Phone Call on Their Anxiety Level During Undergoing Abdominal Cancer Surgery: A Randomized Controlled Trial

Overview

Psychological and physiological issues encountered by family members due to the intraoperative process are factors that complicate the support and care systems of the patient. It is stated that family members of patients undergoing surgery, especially those who do not have sufficient information about the surgical process, experience stress, anxiety, and concern. The need for nursing interventions aimed at providing information about the surgical process, reducing the anxiety levels of family members during the surgery, and supporting them is emphasized. In this context, the study aims to evaluate the effect of periodically informing family members of patients undergoing abdominal cancer surgery via phone during the surgery on their anxiety levels.

Detailed description

Once the patient scheduled for surgery is taken to the operating room, communication between the family members and the surgical team, as well as the patient, is cut off. Family members who do not have any information about the progress of the surgery experience anxiety during the waiting period. High levels of anxiety can limit the family members' ability to understand and process information, affecting their ability to cope with the situation. The high anxiety experienced by family members during the surgery can reflect onto the patient postoperatively, potentially negatively impacting the patient's adaptation, recovery process, and family relations. It is known that family members of patients undergoing cancer surgery experience a higher level of anxiety. The anxiety emerging during this process leads to various physiological and psychological negative consequences for the family members. It is known that informing family members by nurses during surgery helps reduce their anxiety. In this direction, the primary aim of the study is to determine the effect of periodically informing family members of patients undergoing abdominal cancer surgery via phone during the surgery on their anxiety levels. Additionally, the study will evaluate the satisfaction levels of the participants.

Interventions

  • Other Information
    Nurse-led family member information

Primary outcome measures

  • Anxiety [Time frame: During surgery]
Secondary outcome measures (1)
  • Satisfaction with Telephone Information Provided During Surgery [Time frame: Immediately after the surgery.]

Eligibility criteria

Inclusion criteria

  • Being a first-degree relative who has given consent,
  • Being able to understand and speak Turkish,
  • Being literate,
  • Willing to participate in the study,
  • Using a phone,
  • Being present in the hospital before, during, and after the surgery.

Exclusion criteria

  • Having a hearing or speech impairment,
  • Having a psychiatric disorder or using psychiatric medication.

Endpoint Criteria:

  • Inability to reach the participant when called during the surgery,
  • The patient's death during the surgery.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Health services research

Study locations

Turkey (Türkiye) · 1 center
  • Karadeniz Technical University — Trabzon

Identifiers

NCT: NCT06723600 · Nurse_Anxiety

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗