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Completed

NCT Number: NCT07408817

Teleconference-Based Structed Counseling

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.

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Key information

Age range

Up to 80 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bartın Üniversitesi

Bartın, Turkey (Türkiye)

About this study

This randomized controlled study is planned to examine the effect of structured teleconference-based counseling provided before cataract surgery on patients' anxiety levels and predefined postoperative variables. The study will be carried out with patients scheduled for cataract surgery at a public hospital in the Western Black Sea Region. Eligible participants will be randomly assigned to either the intervention group or the control group. Patients in the intervention group will receive structured counseling via teleconference prior to surgery, while those in the control group will receive routine preoperative care. Data will be collected using validated data collection tools, including the Patient Information Form, the State-Trait Anxiety Inventory, the Tele-Nursing Evaluation Form, and the Patient Outcome Form. Anxiety levels and postoperative variables will be assessed at predetermined time points, including preoperative assessment and postoperative follow-up on days 1, 3, and 7. This study aims to contribute to the development of evidence-based nursing practices by evaluating the role of teleconference-based preoperative counseling.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Criteria for inclusion in the study:
  • The patient must be willing to participate in the study
  • There must be no impediments to communication
  • Willingness to cooperate
  • Being 18 years of age or older
  • No diagnosed mental illness
  • Being able to read and write
  • Being able to communicate by telephone
  • Using a smartphone and having an internet connection

Exclusion criteria

  • Not wanting to participate in the study
  • Having previously undergone eye surgery
  • Having a communication barrier
  • Not being open to cooperation
  • Being under 18 years of age
  • Having a diagnosed mental illness
  • Being illiterate
  • Being unable to use communication tools
  • Not having a smartphone and internet connection

Translated with DeepL.com (free version)

Treatment and study plan

Teleconference-Based Structured Preoperative Counseling Program for Cataract Surgery

Behavioral

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.

Routine Preoperative Education and Standard Clinical Care

Behavioral

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

Primary outcomes

  1. Preoperative Anxiety Level

    Time frame: Assessed once at baseline during the preoperative evaluation, within 1-7 days prior to cataract surgery.

    Preoperative anxiety level will be assessed using the State-Trait Anxiety Inventory (STAI).

    The STAI consists of two 20-item subscales: State Anxiety and Trait Anxiety. Each subscale has a total score range of 20 to 80. Higher scores indicate higher levels of anxiety, representing a worse outcome.

Secondary outcomes

  1. Patient Knowledge About Cataract Surgery

    Time frame: Assessed once at baseline during the preoperative evaluation, within 1-7 days prior to cataract surgery.

    Patient knowledge level will be assessed using a structured Patient Knowledge Questionnaire developed for cataract surgery education. Total scores range from 0 to 100, with higher scores indicating greater knowledge about cataract surgery.

  2. Patient Satisfaction With Preoperative Information

    Time frame: Assessed once at baseline during the preoperative evaluation, within 1-7 days prior to cataract surgery.

    Patient satisfaction with preoperative information will be assessed using a structured Patient Satisfaction Questionnaire related to preoperative education. Total scores range from 0 to 100, with higher scores indicating higher patient satisfaction.

  3. Adherence to Preoperative Care Instructions

    Time frame: Assessed once at baseline during the preoperative evaluation, within 1-7 days prior to cataract surgery.

    Adherence to preoperative care instructions assessed using a checklist-based evaluation form.

Sponsors and collaborators

Lead sponsor

Mehtap ÖZTÜRK BAKIR

Other

Collaborators

  • Bartin State Hospital

Registry information

Official study title

The Effect of Structured Counseling Provided Via Teleconference Before Cataract Surgery on Patient Outcomes and Anxiety

Acronym: CAT-TELE

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 13, 2026
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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