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A preoperative program to promote peri- and postoperative health in patients undergoing thoracic aortic surgery: a randomized controlled trial

A preoperative program to promote peri- and postoperative health in patients undergoing thoracic aortic surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22457
Enrollment
56
Registered
2020-10-16
Start date
2021-04-01
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Thoracic aortic disease

Interventions

Patients from the intervention group will start the preoperative physical activity (PA) program as soon as possible after all baseline measurements are completed (T0). The intervention will be termina

Sponsors

Radboudumc, Nijmegen, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: • Scheduled for a preoperative visit at the cardiothoracic surgery outpatient clinic prior to probable thoracic aortic surgery. • Aged 18 years or older. • Able to understand and perform study related procedures.

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: • Unable to provide signed and dated informed consent form. • Wheelchair-bounded or physically unable to stand or walk. • Currently enrolled in another interventional study targeting either sedentary behaviour and/or physical activity.

Design outcomes

Primary

MeasureTime frame
Perioperative sedentary behaviour, i.e. hours spent sitting/lying during waking hours per day.

Secondary

MeasureTime frame
Perioperative physical activity patterns; perioperative maximal handgrip strength; perioperative resting blood pressure; postoperative occurrence of neurological deficits (e.g. stroke or delirium).

Contacts

Public ContactRalf Weijs

Radboud university medical center

Ralf.Weijs@radboudumc.nl+310243613676

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)