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Teleconference-Based Structed Counseling

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07408817
Acronym
CAT-TELE
Enrollment
128
Registered
2026-02-13
Start date
2025-01-31
Completion date
2025-05-31
Last updated
2026-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract Surgery

Keywords

cataract, anxiety, teleconsultation

Brief 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.

Detailed description

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.

Interventions

BEHAVIORALTeleconference-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.

BEHAVIORALRoutine 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

Mehtap ÖZTÜRK BAKIR
Lead SponsorOTHER
Bartin State Hospital
CollaboratorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
No minimum to 80 Months
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Preoperative Anxiety LevelAssessed 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

MeasureTime frameDescription
Patient Knowledge About Cataract SurgeryAssessed 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.
Patient Satisfaction With Preoperative InformationAssessed 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.
Adherence to Preoperative Care InstructionsAssessed 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026