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Anxiety Scores With Media Based Patient Education Before Dilatation and Curettage

K

Kanuni Sultan Suleyman Training and Research Hospital

Status

Completed

Conditions

Anxiety
Abnormal Uterine Bleeding

Treatments

Behavioral: Multimedia- based patient education

Study type

Interventional

Funder types

Other

Identifiers

NCT03930303
Gulseren1

Details and patient eligibility

About

Subjects with abnormal uterine bleeding and scheduled for dilatation and curettage (D&C) will be randomized to a multimedia-based education (MME group) or verbal information (Control group ) before (D&C). State-Trait Anxiety Inventory will be asked by the nursing staff before and after multimedia-based education or verbal information to all patients. Then the patients will undergo (D&C) at an office setting. The impact of MME on patient anxiety will be evaluated by statistical analysis.

Full description

Subjects with abnormal uterine bleeding and scheduled for dilatation and curettage (D&C) with diagnostic or treatment purpose will be randomized to two intervention arms. Multimedia-education Group (MME group) and verbal information group (Control Group). Both groups will receive State-Trait Anxiety Inventory before and after education and then will undergo D&C at an office setting. State-Trait Anxiety Inventory will be asked by the nursing staff. Multimedia-based education will be carried out using a 5 minutes video explaining the details of D&C. D&C will be carried out at office setting by an experienced gynecologist under sedation and analgesia.

Enrollment

102 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Clinical diagnosis of abnormal uterine bleeding Scheduled for dilatation and curettage Must understand the characteristics of the study

Exclusion criteria

Psychological disease Contraindication for hysteroscopy Visual deficit, Auditory deficit

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups

Multimedia Arm
Active Comparator group
Treatment:
Behavioral: Multimedia- based patient education
Control
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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