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Behavioral Intervention

Pedometer follow-up and coaching for Postoperative Outcomes

N/A
Recruiting
Led By Sergio D Bergese, MD, FASA
Research Sponsored by Stony Brook University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Adult subjects ≥18 years at screening
Planned inpatient stay for 1 night or more
Timeline
Screening 3 weeks
Treatment Varies
Follow Up postoperative day 8 to day 30
Awards & highlights

Study Summary

This trial aims to see if using a pedometer with virtual coaching can help patients walk better after major abdominal surgery. They want to know if coaching with the pedometer can increase walking, improve

Who is the study for?
This trial is for individuals recovering from major abdominopelvic surgery. Participants should be willing to use a pedometer app and share their data. Specific inclusion or exclusion criteria are not provided, but typically, patients with complications that prevent walking or using an app may be excluded.Check my eligibility
What is being tested?
The study is testing if remote follow-up via a pedometer app and text message coaching can increase post-surgery walking (ambulation). It's comparing two groups: one gets the app plus coaching, the other just uses the app. The aim is to see if this improves satisfaction and recovery while reducing complications.See study design
What are the potential side effects?
Since this trial involves non-invasive interventions like using a pedometer and receiving text messages, side effects are minimal. However, participants might experience privacy concerns due to data sharing or stress from adhering to ambulation goals.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 18 years old or older.
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I will be staying in the hospital for at least one night.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~postoperative day 8 to day 30
This trial's timeline: 3 weeks for screening, Varies for treatment, and postoperative day 8 to day 30 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Adherence to ambulation goal
Secondary outcome measures
30-day Duke Activity Status Index (DASI) score
30-day Quality of Recovery -15 (QoR-15) score
Patient satisfaction
+4 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Pedometer follow-up and coachingExperimental Treatment2 Interventions
Pedometer follow-up plus text message coaching Monday/ Wednesday/ Friday
Group II: Pedometer follow upActive Control1 Intervention
Pedometer follow-up from day 8- 30 after surgery

Find a Location

Who is running the clinical trial?

Stony Brook UniversityLead Sponsor
216 Previous Clinical Trials
39,851 Total Patients Enrolled
Sergio D Bergese, MD, FASAPrincipal InvestigatorStony Brook Medicine

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are potential candidates still eligible to participate in this ongoing clinical trial?

"As per clinicaltrials.gov, this particular medical study is actively seeking eligible participants. The trial was initially made public on January 31st, 2023 and the most recent update was recorded on February 6th, 2024."

Answered by AI

How large is the participant pool for this particular medical study?

"Yes, according to the information available on clinicaltrials.gov, this research investigation is actively seeking suitable candidates. The trial was first published on January 31st, 2023 and last modified on February 6th, 2024. It aims to recruit a total of 120 participants from one designated site."

Answered by AI
~7 spots leftby Jun 2024