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Teleconference-Based Structed Counseling

NCT07408817 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2026-02-13

No results posted yet for this study

Summary

This study is a randomized controlled trial designed to evaluate the effect of structured teleconference-based counseling provided before cataract surgery on patients' anxiety levels and predefined postoperative outcome measures. The study will be conducted between January 31, 2025, and May 31, 2025, at a public hospital located in the Western Black Sea Region. The study population will consist of patients scheduled for cataract surgery. Eligible participants will be assigned to the intervention or control group using a simple random sampling method. Patients in the intervention group will receive structured teleconference-based counseling prior to surgery, while patients in the control group will receive standard preoperative care. Data will be collected using the Patient Information Form, the State-Trait Anxiety Inventory, the Tele-Nursing Evaluation Form, and the Patient Outcome Form. Participants will be followed up by telephone on postoperative days 1, 3, and 7. Statistical analyses of the collected data will be performed using SPSS version 29.0.

Conditions

  • Cataract Surgery

Interventions

BEHAVIORAL

Teleconference-Based Structured Preoperative Counseling Program for Cataract Surgery

Participants will receive a structured, standardized preoperative counseling program delivered via teleconference in addition to standard care. The intervention will be conducted 1-3 days before cataract surgery as a single session lasting approximately 30-40 minutes and will be delivered by a trained nurse/researcher.

BEHAVIORAL

Routine Preoperative Education and Standard Clinical Care

Participants will receive routine preoperative education and standard clinical care according to institutional protocols. No additional educational or counseling intervention will be provided.

Sponsors & Collaborators

  • Bartin State Hospital

    collaborator OTHER_GOV

  • Mehtap ÖZTÜRK BAKIR

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Max Age
80 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-31
Primary Completion
2025-05-21
Completion
2025-05-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07408817 on ClinicalTrials.gov