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12-week Exercise Intervention Program Versus Observation in Early Stage Breast Cancer Patients on the Impact on Mental Health, Quality of Life and Immune Markers

Primary Purpose

Breast Cancer

Status
Recruiting
Phase
Phase 3
Locations
Singapore
Study Type
Interventional
Intervention
Exercise
Sponsored by
National University Hospital, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female
  • Age 21-70 years
  • Histological or cytological diagnosis of breast carcinoma
  • Stage I-III breast cancer
  • Has undergone curative breast cancer surgery with no clinically measurable tumor
  • Between 4-12 weeks from the last adjuvant radiotherapy or chemotherapy session, if given, whichever is later. Patients who do not receive adjuvant chemotherapy or radiotherapy can be enrolled and will be randomized within 4-12 weeks of breast cancer surgery.
  • Able to sign informed consent
  • Able to adhere to study procedures

Exclusion Criteria:

  • Cardiovascular, respiratory, or musculoskeletal problems that preclude moderate physical activity
  • Major medical problems deemed by the investigator to be unsuitable for enrollment

Sites / Locations

  • National University Hospital, SingaporeRecruiting
  • Tan Tock Seng HospitalRecruiting
  • Ng Teng Fong General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise intervention

Non-exercise

Arm Description

Patients who are randomised to this arm will be enrolled to the exercise programme.

Patients who are randomised to the non-exercise group can continue their daily and physical activities as they normally would.

Outcomes

Primary Outcome Measures

Improved mental health
Based on the HADS (Hospital Anxiety and Depression Scale) questionnaire, we define a score of ≥8/21 as caseness for anxiety or depression

Secondary Outcome Measures

Adherence rate
Subjects are considered to have adhered to the 12-week exercise regimen if they have completed at least 20 scheduled sessions over a period of no longer than 16 weeks

Full Information

First Posted
March 27, 2018
Last Updated
May 8, 2018
Sponsor
National University Hospital, Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT03518957
Brief Title
12-week Exercise Intervention Program Versus Observation in Early Stage Breast Cancer Patients on the Impact on Mental Health, Quality of Life and Immune Markers
Official Title
A Randomized Controlled Study of a 12-week Exercise Intervention Program Versus Observation in Early Stage Breast Cancer Patients on the Impact on Mental Health, Quality of Life and Immune Markers
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Recruiting
Study Start Date
March 12, 2015 (Actual)
Primary Completion Date
December 20, 2021 (Anticipated)
Study Completion Date
December 20, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National University Hospital, Singapore

4. Oversight

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

5. Study Description

Brief Summary
Exercise in early breast cancer patients has the potential to improve depression, anxiety, fatigue, quality of life and even survival. The effects of exercise may come about by way of changes in weight, immune markers and telomere length, but data on this so far has not been conclusive. To better understand the physical, psychological, and biological effects of exercise on breast cancer survivorship, the investigators propose to perform a phase III randomized controlled trial of a 12-week exercise intervention program versus usual care in early stage breast cancer patients, and will follow up the patients prospectively for 5 years, with serial assessment of physical and functional activity, QoL, depression and anxiety scores, telomere length and plasma immune markers.
Detailed Description
In this study, 304 eligible patients will be randomized 1:1 to a 12-week exercise intervention program versus observation, and stratified by two factors: received adjuvant chemotherapy versus not, and age<50 versus age ≥50 years. Breast cancer and its treatment can have both physical and psychological sequelae, which can persist many years after diagnosis. Physical effects include higher rates of pain, fatigue and decline in physical function, while psychological effects include depression and anxiety. In particular, depression spectrum syndromes occur in 20-50% of people with cancer, and in 1.5-46% of people with breast cancer. In a recent study conducted locally at the National University Cancer Institute, Singapore (NCIS), it was found that 27% of newly diagnosed cancer patients have caseness for depression and 44% have caseness for anxiety, as measured using the Hospital Anxiety and Depression scale. Breast cancer is also associated with weight gain - as many as 50-96% of women, especially those undergoing chemotherapy, experience sarcopenic weight gain during treatment, in the range of 2.5-6.2kg. Patients do not tend to return to their pre-diagnosis weight. With respect to quality of life (QoL), poorer QoL occurs in the short term, whereas long-term survivors tend to have a good overall QoL, albeit with an increase in some specific problems like lymphoedema and sexual dysfunction. Some of these measures predict overall survival and risk of recurrence - low levels of psychological distress and low fatigue independently predicted longer recurrence-free and overall survival, and lack of anxiety predicted longer recurrence-free survival. Obesity is also a poor prognostic factor and increases the risk of recurrence. Telomere length (TL), which generally shortens with ageing, may also be implicated - in a study of breast cancer patients with or without insomnia, those with insomnia were reported to have higher rates of depression, fatigue and anxiety, and shorter TLs. Furthermore, breast cancer patients who were engaged in at least moderate physical activity had significantly longer TLs than those who did not, although there was no correlation between depression and shorter TLs in this study.Another study in prostate cancer patients showed that 3 months of comprehensive lifestyle changes after diagnosis was associated with increased telomere lengths and reduced telomerase activity after 5 years of follow-up. To better understand the physical, psychological, and biological effects of exercise on breast cancer survivorship, the investigators propose to perform a phase III randomized controlled trial of a 12-week exercise intervention program versus usual care in early stage breast cancer patients, and will follow up the patients prospectively for 5 years, with serial assessment of physical and functional activity, QoL, depression and anxiety scores, telomere length and plasma immune markers.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
304 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exercise intervention
Arm Type
Experimental
Arm Description
Patients who are randomised to this arm will be enrolled to the exercise programme.
Arm Title
Non-exercise
Arm Type
No Intervention
Arm Description
Patients who are randomised to the non-exercise group can continue their daily and physical activities as they normally would.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
Week 1: Patients will undergo an introductory session where the occupational therapist will assess the general condition and physical fitness of the subjects. Week 1 to Week 12: Group exercise sessions supervised by a physiotherapist, twice per week, each session lasting 1 hour, with no more than 8 participants in each group exercise session. The exercise regimen for each session will be personally tailored for the subjects, and will include stretching, cardiovascular and strength training, and cooling down exercises. Week 12 onwards: Patients will receive phone calls- monthly for the first 6 months and then 3 monthly up to the 2-year mark, to encourage them to continue with their exercise regimen at home.
Primary Outcome Measure Information:
Title
Improved mental health
Description
Based on the HADS (Hospital Anxiety and Depression Scale) questionnaire, we define a score of ≥8/21 as caseness for anxiety or depression
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Adherence rate
Description
Subjects are considered to have adhered to the 12-week exercise regimen if they have completed at least 20 scheduled sessions over a period of no longer than 16 weeks
Time Frame
16 weeks

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Only females will be included, as this is a study on breast cancer
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female Age 21-70 years Histological or cytological diagnosis of breast carcinoma Stage I-III breast cancer Has undergone curative breast cancer surgery with no clinically measurable tumor Between 4-12 weeks from the last adjuvant radiotherapy or chemotherapy session, if given, whichever is later. Patients who do not receive adjuvant chemotherapy or radiotherapy can be enrolled and will be randomized within 4-12 weeks of breast cancer surgery. Able to sign informed consent Able to adhere to study procedures Exclusion Criteria: Cardiovascular, respiratory, or musculoskeletal problems that preclude moderate physical activity Major medical problems deemed by the investigator to be unsuitable for enrollment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Soo Chin Lee
Phone
(65) 6779 5555
Email
soo_chin_lee@nuhs.edu.sg
First Name & Middle Initial & Last Name or Official Title & Degree
Andrea Wong
Phone
(65) 6779 5555
Email
andrea_la_wong@nuhs.edu.sg
Facility Information:
Facility Name
National University Hospital, Singapore
City
Singapore
ZIP/Postal Code
119228
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Soo Chin Lee
Phone
(65) 6779 5555
Email
soo_chin_lee@nuhs.edu.sg
Facility Name
Tan Tock Seng Hospital
City
Singapore
ZIP/Postal Code
308433
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ern Yu Tan
Phone
+65 6357 7807
Email
Ern_Yu_Tan@ttsh.com.sg
First Name & Middle Initial & Last Name & Degree
Soon-U Lawrence Lee
Facility Name
Ng Teng Fong General Hospital
City
Singapore
ZIP/Postal Code
609606
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chuan Chien Tan
Phone
+65 6716 2000
Email
Chuan_Chien_Tan@nuhs.edu.sg

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23041586
Citation
Carayol M, Bernard P, Boiche J, Riou F, Mercier B, Cousson-Gelie F, Romain AJ, Delpierre C, Ninot G. Psychological effect of exercise in women with breast cancer receiving adjuvant therapy: what is the optimal dose needed? Ann Oncol. 2013 Feb;24(2):291-300. doi: 10.1093/annonc/mds342. Epub 2012 Oct 5.
Results Reference
background
PubMed Identifier
12228878
Citation
Kolden GG, Strauman TJ, Ward A, Kuta J, Woods TE, Schneider KL, Heerey E, Sanborn L, Burt C, Millbrandt L, Kalin NH, Stewart JA, Mullen B. A pilot study of group exercise training (GET) for women with primary breast cancer: feasibility and health benefits. Psychooncology. 2002 Sep-Oct;11(5):447-56. doi: 10.1002/pon.591.
Results Reference
background

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12-week Exercise Intervention Program Versus Observation in Early Stage Breast Cancer Patients on the Impact on Mental Health, Quality of Life and Immune Markers

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