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Clinical Trials/ACTRN12620000039987
ACTRN12620000039987
Not Yet Recruiting
N/A

Effectiveness of Home-based Physical Activity for Survivors (HoPS) programme in enhancing physical activity among National Cancer Society Malaysia's Volunteers.

IVERSITI PUTRA MALAYSIA0 sites106 target enrollmentJanuary 21, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
IVERSITI PUTRA MALAYSIA
Enrollment
106
Status
Not Yet Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 21, 2020
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
IVERSITI PUTRA MALAYSIA

Eligibility Criteria

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).

Outcomes

Primary Outcomes

Not specified

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