Pelvic Organ Prolapse Clinical Trial
— GIMPSOfficial title:
Guided IMagery and Patient Satisfaction Following Urogynecological Surgery
Verified date | July 2017 |
Source | Loyola University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
We hypothesize that women who use GIM pre-operatively will feel more prepared for surgery, have less anxiety on the day of surgery and have higher satisfaction scores 6 weeks after surgery compared to women who undergo our routine pre-operative care.
Status | Completed |
Enrollment | 44 |
Est. completion date | December 2016 |
Est. primary completion date | February 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - routine vaginal or laparoscopic surgery for pelvic organ prolapse planned = 1 week from enrollment - a planned overnight hospital stay - commitment to listen to a 15 minute audio Compact Disc daily - proficiency in English. Exclusion Criteria: - Not having routine vaginal or laparoscopic surgery for pelvic organ prolapse planned = 1 week from enrollment - Not a planned overnight hospital stay - Unable to commitment to listen to a 15 minute audio Compact Disc daily - Not proficiency in English. |
Country | Name | City | State |
---|---|---|---|
United States | Loyola University Medical Center | Maywood | Illinois |
Lead Sponsor | Collaborator |
---|---|
Loyola University |
United States,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in patient satisfaction with urogynecological surgery when using GIM (questionnaire) | Women will report their satisfaction with their surgical experience 6 weeks after surgery using a 10-point Likert scale. | 6 weeks | |
Secondary | Change in patient sense of preparedness when using GIM (questionnaire) | Preparedness will be measured at baseline, day of surgery, and 6 weeks after surgery to determine how GIM affected patient preparedness. It will be measured using a 10-point Likert scale | 6 weeks | |
Secondary | Change in patient anxiety about surgery when using GIM (questionnaire) | Patient anxiety will be measured at baseline, day of surgery and at 6 weeks post op to determine how GIM affected anxiety. It will be measured using the State-Trait Anxiety Inventory (STAI), which has been used extensively in research and clinical practice since its introduction in 1966 and is the most widely cited measure of anxiety. | 6 week |
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