Goal Achievement and Patient Satisfaction in Benign Hysterectomy

This study evaluates patient goal achievement and satisfaction in benign hysterectomy. Patient's will state their goals prior to undergoing benign hysterectomy, and will receive a follow-up questionnaire 3 months post-operatively evaluating their perception of goal achievement and overall satisfaction. Goal achievement and satisfaction will be evaluated for association with surgical indication, surgical approach (minimally invasive vs abdominal surgery), and demographic information.

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Key information

Conditions

Hysterectomy Behavior Goal Achievement Health Behavior Minimally Invasive Surgery Patient Satisfaction Treatment Adherence and Compliance

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

University Hospitals

Cleveland, Ohio, 44106, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Patient undergoing hysterectomy for benign indication
Age 18 or greater
English speaking
Access to communication via telephone

Exclusion criteria

Patient undergoing hysterectomy for malignant or pre-malignant condition
Non-english speaking patient
Patient without telephone access
Patient undergoing emergent or unplanned hysterectomy
Vulnerable populations

Treatment and study plan

Questionnaire 3 months post-operatively

Other

Primary outcomes

Goal achievement score of 4 or 5

Time frame: 3 months post-operatively

Patients will state their goals prior to surgery, then at the three months post-operatively will rank if their goals were met on a 1-5 likert scale (1=strongly disagree, 2=disagree, 3=neutral, 4=agree, 5=strongly agree). Goals are considered achieved with a likert score of 4 or 5.

Secondary outcomes

Percent of patient satisfaction

Time frame: 3 months post-operatively

At three months post-operatively, patients will state how satisfied they are with their hysterectomy experience, from 0 to 100%.

Sponsors and collaborators

Lead sponsor

University Hospitals Cleveland Medical Center

Other

Registry information

Important dates

Study start: 2015
Primary completion: 2017
Study completion: 2017
First posted: Dec 3, 2015
Registry last updated: Oct 31, 2017

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.

Published trials that share one or more normalized conditions with this study.

Completed