Surgery Clinical Trial
Official title:
Using Pedometers for the Assessment and Enhancement of Mobility in Gynaecological and Oncological Patients Following Surgery.
NCT number | NCT04711421 |
Other study ID # | 0689-19 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 1, 2020 |
Est. completion date | May 1, 2022 |
Verified date | May 2020 |
Source | Tel-Aviv Sourasky Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a prospective cohort study, planned to study the effects of pedometers (digital step counters) on patient mobility following gynecology and gynecology oncology surgeries. The investigators plan to study the effect of personalized repeated feedback approach based on pedometer results in patients following gynecology and gynecology oncology surgeries.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | May 1, 2022 |
Est. primary completion date | May 1, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 99 Years |
Eligibility | Inclusion Criteria: Patients following gynecology and gynecology oncology surgery Consent to participation No medical recommendation for bed rest and limited mobility Exclusion Criteria: Refusal to participate Medical recommendation to limit mobility |
Country | Name | City | State |
---|---|---|---|
Israel | Tel Aviv Medical Center | Tel Aviv |
Lead Sponsor | Collaborator |
---|---|
Tel-Aviv Sourasky Medical Center |
Israel,
Ganer Herman H, Kleiner I, Tairy D, Gonen N, Ben Zvi M, Kovo M, Bar J, Weiner E. Effect of Digital Step Counter Feedback on Mobility After Cesarean Delivery: A Randomized Controlled Trial. Obstet Gynecol. 2020 Jun;135(6):1345-1352. doi: 10.1097/AOG.0000000000003879. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of steps per day during the hospitalization period | umber of steps taken by patient as recirded by pedometer | Up to 1 week | |
Secondary | Number of participants with complication following surgery | infectious ( wound), blood product transfusion | Up to 1 week | |
Secondary | Number of analgesic doses | Number of doses of analgesics consumed by patient | Up to 1 week | |
Secondary | Length of hospitalization | Duration of hospitalization following surgery | Up to 4 week | |
Secondary | Number of thromboembolic events | hromboembolic events, including deep vein thrombosis and pulmonary emboli | Up to 4 week |
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