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Comparing the application effects of two different early getting out of bed activity guidance strategies in patients after gynecological tumor surgery: a randomized, open, parallel controlled study

Comparing the application effects of two different early getting out of bed activity guidance strategies in patients after gynecological tumor surgery: a randomized, open, parallel controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046035
Enrollment
Unknown
Registered
2021-05-02
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

gynecological tumor surgery

Interventions

Experimental group:the self-fatigue assessment
Control group:pedometer group

Sponsors

Xiangyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Sign an informed consent form before conducting any research procedures; 2. Tumor patients undergoing gynecological surgery; 3. Patients with normal cognitive function; 4. Patients who have normal limb activity before surgery; 5. Have not participated in other research projects in the past 3 years or currently.

Exclusion criteria

Exclusion criteria: 1. Gynecological acute abdomen patients undergoing emergency surgery; 2. Hypertension cannot be well controlled, and diabetes is poorly controlled; 3. Patients with severe liver and kidney dysfunction; 4. Cardiac function level 3 or above. (See Appendix); 5. Patients who have been diagnosed with venous thrombosis of the lower extremities; 6. Elective surgery stroke within 6 months; 7. Patients who are hospitalized for day surgery; 8. Patients who have a history of intestinal obstruction or a high risk of intestinal obstruction; 9. Patients who have been operated on again within the past month; 10. During pregnancy, patients who plan to become pregnant during the study period, who have not taken effective contraceptive measures approved by medicine, and who are breast-feeding; 11. A history of alcohol abuse or drug abuse in the past 12 months; 12. Individuals or investigators judged to be unsuitable for this study who are at risk of compliance or compliance.

Design outcomes

Primary

MeasureTime frame
Postoperative exhaust time (hours);

Secondary

MeasureTime frame
Postoperative hospital stay (days);Patient comfort;Time to first bowel movement;Postoperative complications;The incidence of adverse reactions (nausea, nausea, dizziness);Patient satisfaction;Hospital costs;Sleep time at night;Sleep quality;Patient compliance;

Countries

China

Contacts

Public ContactHuang Xiaojie

Xiangyang Central Hospital

19935430@qq.com+86 13995783762

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026