Physical activity intervention programme for cancer survivors to improve physical activity level

Not Applicable

• Conditions: Breast Cancer; Colorectal cancer; Cancer - Breast; Cancer - Bowel - Back passage (rectum) or large bowel (colon)

• Registration Number: ACTRN12620000039987
• Lead Sponsor: IVERSITI PUTRA MALAYSIA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-01-21
• Last Update Posted: 3 February 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 106

Inclusion Criteria

i.Malaysian citizen breast or colorectal cancer patient between the age of 18 years old and 65 years old who are registered with National Cancer Society Malaysia (NCSM) and are actively involved with 3 branches of NCSM at Kuala Lumpur, Negeri Sembilan and Melaka
ii. Stage I to III (or IIIA for breast cancer) who are not currently receiving (and do not plan to receive during the duration of study enrollment) chemotherapy or radiation therapy
iii.More than 8 weeks post-surgical procedure
iv. Post-treatment three months
v.Obtained medical clearance from physician
vi. Grade 0 or 1 for ECOG Performance Status

Exclusion Criteria

i. Participating, on average, 30 to 60 min per day (greater than or equal to 150 min per week) of moderate intensity for at least 5 days per week or 20 to 30 min per day (greater than or equal to 75min per week) of vigorous intensity for at least 5 days per week or an equivalent combination of the two
ii. Medical or psychological condition that would interfere with the ability to fully participate during the study enrollment (e.g., psychosis, schizophrenia, etc.)
iii. Recurrent disease,
iv. Elective surgery planned during the duration of the intervention that would interfere with intervention participation (e.g., breast reconstructive surgery), and
v. Planned travel that interferes with the scheduled study sessions (i.e., no travel in the first 4 weeks and no travel in the last week of the intervention).

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Total MET-minutes/week using validated IPAQ [Baseline, at 8-week (immediately after intervention) and at 16-week post intervention]