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Physical Rehabilitation Among Patients Undergoing Radical Cystectomy Due to Urinary Bladder Cancer (CanMoRe)

Primary Purpose

Urinary Bladder Cancer

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
The CanMoRe programme
Home exercise
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Bladder Cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who are planned for a robotic assisted laparoscopic radical cystectomy due to urinary bladder cancer at the Karolinska University Hospital Solna will be included in the trial. The patients should be able to talk and understand Swedish, live in the Stockholm County Council area and be mobile with or without walking aid.

Exclusion Criteria:

  • Patients who will undergo radical cystectomy on a non-curative basis will not be included.

Sites / Locations

  • Karolinska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Individualized exercise

Active control group

Arm Description

The intervention group get a referral to physiotherapist in Primary Health Care in Stockholm County Council, close to where they live. Within the third week after discharge, the patients begin twelve weeks of biweekly exercise. The physical exercise is individually targeted aerobic and strength exercises, based on international recommendations for persons with cancer disease. The program is approved by resposible surgeons.

Oral and written information of a home-based exercise programme and information of supportive techniques to improve physical activity

Outcomes

Primary Outcome Measures

Six-minute walk test
The test reproduces activity of daily living at a sub maximal level. Output: meters Score: 0-900.

Secondary Outcome Measures

ActivPAL accelerometer
Habitual physical activity, measured for 7 consecutive days. Output: number of steps per day.
Chair stand test
Measure of leg strength. Output: Scale 0-30
Hand grip strength
Measure of hand grip strength (Jamar hand dynamometer). Output: Kilo 0-60
European Organisation for Research and Treatment of Cancer (EORTC) Quality of life for cancer patients QLQ-C30
Health related quality of life. Output: Scale 0-100. A higher score is worse outcome. For more information see https://qol.eortc.org/questionnaires/
EORTC QLQ-BLM30
Health related quality of life specific for bladder cancer Output: Scale 0-100, a higher score is worse
Piper Fatigue Scale
Fatigue. Output: Scale 0-10. A higher score is worse, i.e more fatigue
Numeric rating scale (NRS)
Pain. Output: Scale 0-10, A higher score is worse i.e more pain
Hospital Anxiety and Depression Scale (HADS)
Psychological wellbeing. Output: Scale 0-21. A higher score is worse
Readmission
Readmissions to hospital. Output: Yes/No
Complications
Complications such as Pneumonia Output: according to Clavien - Dindo classification
Six-minute walk test
The test reproduces activity of daily living at a sub maximal level. Output: meters Score: 0-900.

Full Information

First Posted
June 7, 2019
Last Updated
October 10, 2023
Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03998579
Brief Title
Physical Rehabilitation Among Patients Undergoing Radical Cystectomy Due to Urinary Bladder Cancer
Acronym
CanMoRe
Official Title
The Effect of Physical Rehabilitation Among Patients Undergoing Radical Cystectomy Due to Urinary Bladder Cancer - the CanMoRe Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
November 15, 2022 (Actual)
Study Completion Date
June 20, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of the CanMoRe study is to evaluate the impact of a standardized and individually adapted exercise intervention in Primary Health Care aiming at improving physical function (primary outcome) and habitual physical activity, health related quality of life, fatigue and psychological well-being in patients undergoing radical cystectomy due to urinary bladder cancer.
Detailed Description
The most common treatment for solid cancer tumours is surgery, often in combination with chemo- and/or radiotherapy. To minimise the postoperative complications is important in today's health care. Early mobilisation at the ward and physical activity at home after discharge, have been shown to be important parts to reduce complications. Common complications after abdominal surgery are postoperative pulmonary complications and venous thrombosis. One of the conditions that suffers the most from different kinds of postoperative complications is radical cystectomy due to urinary bladder cancer. Complications after radical cystectomy could be direct related to the patients' high age and also high degree of comorbidity. There is today strong evidence that physical activity has a positive impact on health, survival and quality of life. Patients who have been treated for urinary bladder cancer are not sufficiently physical active and suffer from readmissions to hospital due to complications. Therefore, there is a need for developing and testing a physical rehabilitation programme to support patients who have a radical cystectomy, in the early postoperative period. The CanMoRe study is a randomized controlled trial with a single-blinded design evaluating an exercise intervention in Primary Health Care as part of the CanMoRe programme. In addition, a qualitative study (interviews) on patient's experience of the programme will be conducted as well as data gathered on factors that might influence the implementation of the programme. Then CanMoRe programme consists of preoperative information, the Activity Board used for enhanced mobilization during hospital stay, a 12-week, (1 h, 2 times/week) standardized and individually adapted exercise intervention in Primary Health Care and behavioral support for daily physical activity. The CanMoRe programme is evaluated in two steps, i.e. the in-hospital intervention using the Activity Board (published) and the exercise intervention in Primary Health Care reported herein.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Bladder Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Individualized exercise
Arm Type
Experimental
Arm Description
The intervention group get a referral to physiotherapist in Primary Health Care in Stockholm County Council, close to where they live. Within the third week after discharge, the patients begin twelve weeks of biweekly exercise. The physical exercise is individually targeted aerobic and strength exercises, based on international recommendations for persons with cancer disease. The program is approved by resposible surgeons.
Arm Title
Active control group
Arm Type
Active Comparator
Arm Description
Oral and written information of a home-based exercise programme and information of supportive techniques to improve physical activity
Intervention Type
Other
Intervention Name(s)
The CanMoRe programme
Intervention Description
An exercise intervention in Primary Health Care
Intervention Type
Other
Intervention Name(s)
Home exercise
Intervention Description
An active control group
Primary Outcome Measure Information:
Title
Six-minute walk test
Description
The test reproduces activity of daily living at a sub maximal level. Output: meters Score: 0-900.
Time Frame
Change from baseline to after 12 weeks intervention
Secondary Outcome Measure Information:
Title
ActivPAL accelerometer
Description
Habitual physical activity, measured for 7 consecutive days. Output: number of steps per day.
Time Frame
Measurement 1: Baseline, Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge
Title
Chair stand test
Description
Measure of leg strength. Output: Scale 0-30
Time Frame
Measurement 1: Baseline, Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge
Title
Hand grip strength
Description
Measure of hand grip strength (Jamar hand dynamometer). Output: Kilo 0-60
Time Frame
Measurement 1: Baseline, Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge,
Title
European Organisation for Research and Treatment of Cancer (EORTC) Quality of life for cancer patients QLQ-C30
Description
Health related quality of life. Output: Scale 0-100. A higher score is worse outcome. For more information see https://qol.eortc.org/questionnaires/
Time Frame
Measurement 1: Baseline Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge
Title
EORTC QLQ-BLM30
Description
Health related quality of life specific for bladder cancer Output: Scale 0-100, a higher score is worse
Time Frame
Measurement 1: Baseline Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge
Title
Piper Fatigue Scale
Description
Fatigue. Output: Scale 0-10. A higher score is worse, i.e more fatigue
Time Frame
Measurement 1: Baseline, Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge
Title
Numeric rating scale (NRS)
Description
Pain. Output: Scale 0-10, A higher score is worse i.e more pain
Time Frame
Measurement 1: Baseline, Measurement 2: After 12 weeks intervention. Measurement 3: 1 year after discharge
Title
Hospital Anxiety and Depression Scale (HADS)
Description
Psychological wellbeing. Output: Scale 0-21. A higher score is worse
Time Frame
Measurement 1: Baseline, Measurement 2: 12 weeks. Measurement 3: 1 year after discharge
Title
Readmission
Description
Readmissions to hospital. Output: Yes/No
Time Frame
Collected from journals using standardized time frames at 30 and 90 days
Title
Complications
Description
Complications such as Pneumonia Output: according to Clavien - Dindo classification
Time Frame
Collected from journals using standardized time frames at 30 and 90 days
Title
Six-minute walk test
Description
The test reproduces activity of daily living at a sub maximal level. Output: meters Score: 0-900.
Time Frame
Measurement 3: 1 year after discharge

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who are planned for a robotic assisted laparoscopic radical cystectomy due to urinary bladder cancer at the Karolinska University Hospital Solna will be included in the trial. The patients should be able to talk and understand Swedish, live in the Stockholm County Council area and be mobile with or without walking aid. Exclusion Criteria: Patients who will undergo radical cystectomy on a non-curative basis will not be included.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Hagstromer, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
17176
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32842975
Citation
Porserud A, Karlsson P, Rydwik E, Aly M, Henningsohn L, Nygren-Bonnier M, Hagstromer M. The CanMoRe trial - evaluating the effects of an exercise intervention after robotic-assisted radical cystectomy for urinary bladder cancer: the study protocol of a randomised controlled trial. BMC Cancer. 2020 Aug 26;20(1):805. doi: 10.1186/s12885-020-07140-5.
Results Reference
background
Links:
URL
https://ki.se/en/nvs/the-abdmore-project-2016-2020
Description
The link to the larger project to which this RCT belong

Learn more about this trial

Physical Rehabilitation Among Patients Undergoing Radical Cystectomy Due to Urinary Bladder Cancer

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