Pedometer Intervention and Health Effects for Sedentary Colorectal Cancer Patients During Adjuvant Chemotherapy

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Unknown status
CT.gov ID
NCT02522520
Collaborator
Copenhagen University Hospital at Herlev (Other), Novo Nordisk A/S (Industry), Danish Cancer Society (Other), TrygFonden, Denmark (Industry)
21
1
2
60
0.3

Study Details

Study Description

Brief Summary

Colorectal cancer is one of the most common cancers in Denmark, annually 4,200 men and women are diagnosed and approx. 2000 patients die of their colorectal cancer. As with other cancers, the risk of colorectal cancer increases with age, and the median age at diagnosis is 71 years. Improved treatment has increased the number of survivors with an expected 5-year survival rate of 50-60%. Characteristic of this group of patients is that at the time of diagnosis they often live with comorbidities and have limited leisure time physical activity.

There is evidence that rehabilitation in the form of physical exercise for cancer patients after their initial treatment has a positive effect on a number of physical and psychological parameter such as health-related quality of life, physical capacity and physical function, fatigue, anxiety and depression. However, the most frequently studied diagnosis group is women with breast cancer. Until now only few studies have evaluated the effects of physical activity among colorectal cancer patients receiving chemotherapy

The purpose of this study is: to examine the effect of two different training initiatives - 12 weeks progressive, high-intensity training versus low intensity exercise intervention - on physical, emotional and social habitus, in sedentary patients with colorectal cancer during adjuvant chemotherapy.

The hypothesis of the study are: 1. That both interventions will show a positive association between increased physical capacity (measured by aerobic capacity VO2-peak / peak oxygen uptake) and improved physical function, reduced fatigue and anxiety in the included sedentary colorectal cancer patients undergoing adjuvant chemotherapy.

Participants: Patients undergoing adjuvant chemotherapy for colorectal cancer who have self-reported physical activity level below the national recommended levels (less than 150 min/week of moderate leisure time physical activity, and exercises at least 20 minutes of strenuous physical activity twice a week).

Benefits and risks of participating: Possible benefits of the interventions: to reduce treatment related symptoms and side-effects, increase vitality and well-being and promote lifestyle changes among sedentary colorectal cancer patients receiving adjuvant chemotherapy. At participation in the interventions minor sports injuries may occur.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Pedometer intervention
  • Behavioral: Pedometer + hospital based intervention
  • Device: Omron Walking Style pro. 20
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
21 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Primary outcome (VO2 peak) Physiological tests assessors blinded
Primary Purpose:
Other
Official Title:
Pedometer Intervention, Health Counseling, Symptom Management for Sedentary Colorectal Cancer Patients During Adjuvant Chemotherapy.Two-armed Randomized Phase II Trial
Study Start Date :
Jun 1, 2015
Anticipated Primary Completion Date :
Jun 1, 2020
Anticipated Study Completion Date :
Jun 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Pedometer intervention

Individual progressive pedometer intervention of low to moderate intensity. Furthermore, the patients receive individual health counseling and symptom management counseling to support behavioral change towards increased physical activity.

Behavioral: Pedometer intervention
12 weeks physical activity intervention (supervised/non-supervised)

Device: Omron Walking Style pro. 20
Other Names:
  • Pedometer
  • Active Comparator: Pedometer + hospital based intervention

    Individual progressive pedometer intervention and 5 sessions supervised interval walking + followed by supervised hospital-based intervention of moderate to high-intensity Furthermore, the patients receive individual health counseling and symptom management counseling to support behavioral change towards increased physical activity.

    Behavioral: Pedometer + hospital based intervention
    12 weeks physical activity intervention (supervised/non-supervised)

    Device: Omron Walking Style pro. 20
    Other Names:
  • Pedometer
  • Outcome Measures

    Primary Outcome Measures

    1. Maximum oxygen uptake - ( VO2 peak) [12 weeks]

      Assessed with objective physiological test

    Secondary Outcome Measures

    1. Health related Quality of Life [From baseline to 39 weeks]

      Assessed by The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire, specifically for colon cancer patients

    2. Symptoms and side-effects [From baseline to 39 weeks]

      Assessed by MD Andersen symptom questionnaire and The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire, chemotherapy-induced peripheral neuropathy

    3. Anxiety and Depression [From baseline to 39 weeks]

      Assessed by The Hospital Anxiety and Depression Scale

    4. Lifestyle factors [From baseline to 39 weeks]

      Assessed by smoking cessation, alcohol, diet

    5. Physical activity level [From baseline to 39 weeks]

      Assessed by the International Physical Activity Questionnaire

    6. Dual Energy X-ray Absorptiometry scan [From baseline to 39 weeks]

      Assessed by dual energy x-ray absorptiometry.

    7. Blood cholesterols [From baseline to 39 weeks]

      Assessed by blood samples

    8. Blood pressure / pulse [From 6 to 12 weeks]

      Assessed by Heart Rate Monitor during the hospital-based intervention

    9. Pedometer Step Count [From baseline to 12 weeks]

      Assessed by Omron Walking Style pro. 20 with electronic data transmission

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosed with colorectal cancer in adjuvant chemotherapy

    • Age 18+ years

    • WHO performance status of 0 or 1

    • Undergone surgery at least 6 weeks ago

    • Do not meet criteria for recommended physical activity level of 150 min / week of moderate leisure time physical activity, and exercises at least 20 minutes of strenuous physical activity twice a week.

    Exclusion Criteria:
    • Myocardial infarction within the past six months

    • Symptomatic heart failure

    • Known angina pectoris

    • Contraindication for moderate to strenuous physical activity

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rigshospitalet Copenhagen Denmark 2100

    Sponsors and Collaborators

    • Rigshospitalet, Denmark
    • Copenhagen University Hospital at Herlev
    • Novo Nordisk A/S
    • Danish Cancer Society
    • TrygFonden, Denmark

    Investigators

    • Study Director: Lis Adamsen, Professor, Rigshospitalet, Denmark

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Christina Andersen, RN, MPH, Ph.D., Rigshospitalet, Denmark
    ClinicalTrials.gov Identifier:
    NCT02522520
    Other Study ID Numbers:
    • CIRE-15
    First Posted:
    Aug 13, 2015
    Last Update Posted:
    Mar 11, 2020
    Last Verified:
    Mar 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Christina Andersen, RN, MPH, Ph.D., Rigshospitalet, Denmark
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 11, 2020