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Impact of Patient Education on Preoperative Anxiety and Postoperative Psychosocial Outcomes

V

Vilnius University

Status

Enrolling

Conditions

Preoperative Anxiety

Treatments

Behavioral: Contact education
Behavioral: Virtual education

Study type

Interventional

Funder types

Other

Identifiers

NCT05208580
2021/5-1351-823

Details and patient eligibility

About

The aim of the study is to investigate the effect of preoperative patient education on the level of properative anxiety and postoperative psychosocial outcomes. Participants will be assigned to one of the 3 study groups: on-line education, contact education and control (no preoperative education). The investigators will evaluate preoperative anxiety level at different time points (baseline at 2 weeks before the surgery, at the evening before the surgery and postoperatively) and investigate dynamics of anxiety in the perioperative period. Additional qualitative interview by psychologists will be performed to evaluate the potential causes of increased/decreased preoperative anxiety.

Impact on postoperative complications, well-being of the participant, quality of recovery and satisfaction with medical care will also be evaluated.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • agreement to participate in the study
  • elective cholecystectomy or colon surgery

Exclusion criteria

  • refusal to participate in the study
  • do not speak Lithuanian
  • do not pass the PHQ-2 depression screening test

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

500 participants in 3 patient groups

On-line education
Experimental group
Description:
Virtual educational activities
Treatment:
Behavioral: Virtual education
Contact education
Experimental group
Description:
Live educational classes
Treatment:
Behavioral: Contact education
Control group
No Intervention group
Description:
Regular perioperative care without additional educational activities

Trial contacts and locations

1

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Central trial contact

Egle Kontrimaviciute, MD, PhD

Data sourced from clinicaltrials.gov

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