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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05887531
Other study ID # malcazar
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2023
Est. completion date October 10, 2024

Study information

Verified date May 2024
Source Universitat Jaume I
Contact Suárez María Pilar
Phone +34 964387804
Email malcazar@uji.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this research is to determine the effectiveness of a Prehabilitation consultation in self-care and physical exercise aimed at patients diagnosed with abdominopelvic cancer with initial surgical indication as part of their therapeutic plan.


Recruitment information / eligibility

Status Recruiting
Enrollment 66
Est. completion date October 10, 2024
Est. primary completion date July 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Majority (greater than or equal to 18 years). - Diagnosis of abdominopelvic cancer and initial surgical indication as part of its therapeutic plan from the General Surgery Services of the General University Hospital of Castellón. - Ability to give informed consent. Exclusion Criteria: - Inability to understand the information provided or insufficient knowledge of the Spanish language. - Inability to carry out the scheduled intervention according to the physician's criteria. - Neoadjuvant treatment to colorectal surgery.

Study Design


Intervention

Other:
Prehabilitation
Patients will be included in a prehabilitation program

Locations

Country Name City State
Spain Universitat Jaume I Castellón De La Plana Castellón

Sponsors (1)

Lead Sponsor Collaborator
Universitat Jaume I

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post-surgical recovery time To determine if there is a reduction in post-surgical recovery time until the start of adjuvant therapy in patients with abdominopelivoc cancer after their incorporation into the Prehabilitation program in self-care and directed physical exercise. More than 2 days
Primary Post-surgical readmisions To determine if there is a reduction in the number of readmisions in patients with abdominopelvic cancer after their incorporation into the Prehabilitation program in self-care and directed physical exercise. until 4 weeks from surgery
Secondary Self-care capacity To know if there is an improvement in the self-care capacity mesured by the Appraisal of Self-care Agency Scale (ASA) scale in patients with abdominopelvic cancer after their incorporation into the Pre-habilitation program in self-care and directed physical exercise. Minimum value: 24 y Maximum value: 96. Higher scores mean a better outcomes. before surgery
Secondary Anxiety levels To establish whether there is a decrease in preoperative anxiety levels mesured by Hospital Anxiety and Depression Scale in patients with abdominopelvic cancer after their incorporation into the Prehabilitation program in self-care and directed physical exercise. before surgery
Secondary Aerobic capacity To determine if there is an improvement in aerobic capacity mesured by walking test in patients with abdominopelvic cancer after their incorporation into the Prehabilitation program in self-care and directed physical exercise. Higher scores mean a better outcomes. before surgery
Secondary Flexibility To determine if there is an improvement flexibility mesured by set and reach test in patients with abdominopelvic cancer after their incorporation into the Prehabilitation program in self-care and directed physical exercise. Higher scores mean a better outcomes. before surgery
Secondary Strength To determine if there is an improvement strength mesured by hand grip in patients with abdominopelvic cancer after their incorporation into the Prehabilitation program in self-care and directed physical exercise. before surgery
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