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The Effect of Information and Coping With Anxiety Training Given to Women Before Hysterectomy on Their Level of Anxiety

The Effect of Information and Coping With Anxiety Training Given to Women Before Hysterectomy on Their Level of Anxiety: A Post-Test Randomized Controlled Experimental Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05436691
Enrollment
59
Registered
2022-06-29
Start date
2018-07-15
Completion date
2018-12-15
Last updated
2024-03-21

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

Conditions

Anxiety, Hysterectomy

Brief summary

Purpose: In this study, it was aimed to determine the effect of information and coping with anxiety training given to women before they undergo hysterectomy on their anxiety levels. Design and Methods: The parallel group post-test randomized controlled experimental design was used in the study. The study sample comprised 59 women.

Interventions

OTHERInformation and Coping with Anxiety Training

Informing and Coping with Anxiety Training was given to the experimental group before the operation through a prepared booklet.The information booklet about the training was created by the researchers by reviewing the current literature. The booklet provides information for patients scheduled for hysterectomy about how to cope with surgery-related anxiety. The booklet provides information on what the hysterectomy is, why it is performed, what risks it has, what should be done before, during and after the hysterectomy, what rules the patient should comply with after hysterectomy, in which cases she should present to the health institution, what changes she might experience in her social, physical, sexual and emotional life after the surgery. The booklet also provides information about discharge training and coping with anxiety.

Sponsors

Mersin Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* agreeing to participate in the study, * being able to speak and understand Turkish, * being in the age group of 18-65 years, * being admitted to the aforementioned clinic with a planned hysterectomy surgery, * not having any health problems preventing the person from hearing and speaking, * being conscious, being oriented and cooperated, * not having received any training on hysterectomy before the surgery and during discharge.

Exclusion criteria

* not agreeing to participate in the study, * not being able to speak and understand Turkish, * being under the age group of 18 years, * not being admitted to the aforementioned clinic with a planned hysterectomy surgery, * having any health problems preventing the person from hearing and speaking, * not being conscious, being oriented and cooperated, * having received any training on hysterectomy before the surgery and during discharge.

Design outcomes

Primary

MeasureTime frameDescription
Anxiety was assessed using the State-Trait Anxiety Scale.preoperativeThe total score obtained from both scales varies between 20 and 80. It states that 0-19 points mean no anxiety, 20-39 points mean mild, 40-59 points mean moderate, 60-79 points mean severe anxiety, and individuals with a score of 60 and above need professional help

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026