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Feasibility of supervised home-based exercise prehabilitation in patients scheduled for pancreatic resection

Feasibility of supervised home-based exercise prehabilitation in patients scheduled for pancreatic resection - Home-based prehabilitation in pancreatic resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON52089
Enrollment
30
Registered
2021-09-16
Start date
2022-04-04
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Pancreas resection pancreas surgery

Interventions

Patients will participate in a four-week (partly) supervised home-based exercise training program before surgery (12 sessions in total). An advanced cycle ergometer (Lode Corival, Lode BV, Groningen

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate, a subject must meet all of the following criteria: • more than 18 years of age; • scheduled for elective pancreatic resection at Maastricht UMC+, at the University Medical Center Groningen, or at the 'Città della Salute e della Scienza' Hospital in Torino; • willing to participate in the home-based prehabilitation program; • providing informed consent to participate.

Exclusion criteria

Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study: • patients requiring acute (emergency) surgery; • patients undergoing surgery in another hospital; • patients not living within the catchment area of the hospital (

Design outcomes

Primary

MeasureTime frame
The main study parameter/endpoint is the feasibility of the supervised home-based prehabilitation program. Hereto, participation rate and reasons for non-participation will be evaluated. In participating patients, adherence/compliance, dropout rate, reasons for dropout, adverse events, patient motivation, and patient appreciation will be assessed throughout the program. Moreover, therapist appreciation will be determined.

Secondary

MeasureTime frame
Secondary parameters/endpoints before and after the prehabilitation program include aerobic capacity, body composition, functional mobility, immune system function, perceived fatigue, and quality of life. When possible muscle function will be determined before and after the intervention. During the program, progression in physical fitness will be objectively monitored, as well as body mass.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)