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Early Mobilization After Colorectal Surgery

Facilitation of Early Mobilization After Colorectal Surgery: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02131844
Enrollment
100
Registered
2014-05-06
Start date
2014-08-31
Completion date
2016-05-31
Last updated
2018-03-05

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

Conditions

Colonic Diseases, Rectal Diseases

Keywords

colorectal surgery, postoperative recovery, early mobilization

Brief summary

Early mobilization (i.e. initiation of out of bed activities from the day of surgery) is considered an important component of postoperative care after colorectal surgery. Having a health professional dedicated to facilitate early mobilization has the potential to enhance postoperative recovery by preventing the negative effects of prolonged bed rest (e.g. increased risk for complications, muscle loss, deconditioning and functional decline); however, the need to implement this resource-intensive approach is not evidence based. This study aims to contribute evidence about the role of facilitated early mobilization as a strategy to enhance recovery after colorectal surgery.

Detailed description

The primary research question of this study is: to what extent does postoperative facilitation of early mobilization impact on recovery of functional walking capacity at 4 weeks after surgery in comparison to standard care (preoperative education). The hypothesis is that, by 4 weeks after surgery, facilitated early mobilization will result in a greater proportion of participants returning to preoperative levels of functional walking, as measured by the six-minute walk test (6MWT).

Interventions

OTHERFacilitated early mobilization

Participants randomized to this group, in addition the preoperative education (usual care), will have early mobilization facilitated by a trained health professional. This health professional will: (1) visit the participant on the day of surgery to reinforce mobilization goals and assist with transfer to a chair and (2) visit the participant three times per day starting from POD 1 to reinforce mobilization goals and walk with the participant (at least the length of the hallway). Targeted walking distances will increase according to the participant's tolerance. This intervention will be undertaken until POD 3 or hospital discharge, whichever comes first.

OTHERUsual care

Participants randomized to this group will receive instructions about postoperative mobilization in a preoperative education session and will receive a booklet describing mobilization goals for each POD (sit in a chair for 2 hours on the day of surgery, stay out of bed for at least 6 hours/day from POD 1 until hospital discharge)

Sponsors

Mitacs
CollaboratorINDUSTRY
McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult people (\>18 years) * Colonic or rectal diseases (i.e. cancer, inflammatory bowel disease, diverticulitis) planned for surgical resection

Exclusion criteria

* Metastatic disease * Medical conditions that preclude postoperative mobilization (e.g. neurological or musculoskeletal diseases) * Inability to understand English or French * Admission to intensive care immediately after the surgery

Design outcomes

Primary

MeasureTime frameDescription
Functional walking capacity (six-minute walk test)before surgery; 4 weeks after surgeryThe outcome of interest will be the proportion of participants returning to preoperative levels of functional walking capacity at 4 weeks after surgery (within an estimated measurement error of 20 meters)

Secondary

MeasureTime frameDescription
Time to readiness for dischargeduration of hospital stay (expected average of 3 days after surgery)Time to achieve standardized hospital discharge criteria (tolerance of oral intake, recovery of lower gastrointestinal function, adequate pain control on oral analgesia, ability to mobilize and self care and no evidence of complications or untreated medical problems).
Time to recovery of gastrointestinal motilityExpected average of 2 days after surgeryTime to achieve criteria for recovery of gastrointestinal transit (tolerance of solid diet and bowel movement)
Postoperative fatigue (Multidimensional Fatigue Inventory)before surgery; POD 1, 2 and 3; 2 weeks after surgery; 4 weeks after surgery.
Self-reported physical activity status (Duke Activity Status Index)before surgery; 2 weeks after surgery; 4 weeks after surgery
Time out of bed (sitting and standing)postoperative day (POD) 0, 1, 2 and 3Measured by an activity monitor (Actigraph) worn over the participants' hip
Condition-specific health-related quality of life (Abdominal Surgery Impact Scale)before surgery; POD 1, 2 and 3; 2 weeks after surgery; 4 weeks after surgery
Generic heath-related quality of life (RAND-36)before surgery; 4 weeks after surgery
Postoperative complicationsup to 4 weeks after surgeryClassified according to Clavien-Dindo Index and converted into a continuous scale using the Comprehensive Complication Index
Pulmonary function (spirometry)before surgery; POD 1, 2 and 3; 4 weeks after surgeryForced vital capacity (FVC), forced expiratory volume in one second (FEV1) and cough expiratory flow (CEF) will be recorded
Mobility (Life-Space Mobility Assessment)before surgery; 4 weeks after surgery

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026