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Feasibility of Home-based Preoperative Exercise in Older People

Not Applicable
Completed
Conditions
Colorectal Cancer
Interventions
Other: Exercise
Registration Number
NCT02895464
Lead Sponsor
Karolinska Institutet
Brief Summary

The purpose of the study is to evaluate the feasibility of recruitment procedure, intervention including compliance and the collaboration between in- and out patient clinics of preoperative home-based exercise in older people before colorectal surgery.

Detailed Description

The feasibility study will be conducted in order to evaluate the study design of a future RCT. Feasibility data will eg. consist of study flow description, number of eligible participants, included participants, patients and instructors satisfaction with the intervention, training compliance, reasons for drop-outs, and adverse events.

Patients waiting for colorectal surgery will be recruited and included after informed consent. Physical and respiratory function will be assessed at the hospital before the intervention, the day before surgery and the day before discharge. Data on postoperative complications, length of stay and mortality will be collected during the hospital stay. At baseline and six months after surgery, the participants will receive three questionnaires about level of independence in daily living, physical activity and health related quality of life. The intervention will be performed in the older person's home and consists of a combination of high-intensity respiratory training and individually adjusted functional exercise. Both groups will receive physical activity advice and malnutrition will be screened to optimize their nutritional status.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
23
Inclusion Criteria
  • Age above 70, understand and speaks the Swedish language. Surgery due to cancer
Exclusion Criteria
  • Health status that contradicts participation in the study such as unstable heart disease or severe orthopaedic conditions that prohibits training and severe systematic illness.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control groupExerciseThe participants will receive ordinary preoperative information, but will also be encouraged to follow the recommendation of 150 minutes/week of moderate physical activity.
Exercise groupExerciseThe sessions will be led by a physiotherapist, in the older person's home. The sessions will consist of inspiratory muscle training with a resistance starting from 50% of their maximal capacity (30 breathes, 2 times/day). The training session will also consist of high-intensity individually adjusted functional strength and endurance training: chair-stand; stair climb/step up with weight belts, interval walking indoor and/or outdoor. This will be combined with functional task-exercises. The training will be conducted 2-3 times week, for at least two weeks or until they undergo surgery. During the remaining days, the participants will be instructed to follow the recommendation of 30 minutes of moderate physical activity per day, as well as to perform inspiratory muscle training.
Primary Outcome Measures
NameTimeMethod
Recruitment RateBaseline

The recruitment rate is calculated by the number of participants allocated to either the exercise group or control group from the total number of eligible participants (n=66).

Exercise ComplianceAt the end of the intervention, after 2-4 weeks

Compliance with the exercise intervention was defined as the number of sessions attended out of planned sessions and was registered in the exercise logs by the physiotherapists in primary care. Only participants randomized to the exercise group were evaluated for this assessment.

AcceptabilityAt the end of the intervention, after 2-4 weeks

Patients and instructors satisfaction with the intervention measured with a survey. Instructors were not enrolled. Only participants randomized to the exercise group were evaluated for this assessment.

Adverse EventsDuring the intervention, after 1-4 weeks

Musculoskeletal-related events, cardiovascular episodes, falls and health care use that occurred during the exercise intervention before (pre)-surgery. Adverse events are only reported for the intervention group since the control group were a treatment as usual (TAU) group.

Secondary Outcome Measures
NameTimeMethod
Six-minute WalkBaseline, before surgery (after 2-4 weeks), before discharge app 4-10 days after surgery

Meters completed, effort estimated

Inspiratory Muscle StrengthBaseline, before surgery (after 2-4 weeks), before discharge app 4-10 days after surgery

Inspiratory muscle strength measured with MicroRPM.

Chair-stand 30-secBaseline, before surgery (after 2-4 weeks), before discharge app 4-10 days after surgery

Number of stands during 30 sec.

Walking SpeedBaseline, before surgery (after 2-4 weeks), before discharge app 4-10 days after surgery

Normal walking speed was measured over 10 meters.

Postoperative ComplicationsWithin the first 30 days of surgery

Clavien-Dindo, number of participants with at least one postoperative complication.

Length of StayAt discharge, 2-4 weeks after baseline

Number of days admitted to the hospital

Trial Locations

Locations (1)

Stockholm South General Hospital

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Stockholm, Sweden

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