Skip to content

A peer support program for the long-term maintenance of physical activity and health outcomes in breast, prostate and colorectal cancer survivors

The PEER Study: Peer support for the maintenance of high intensity interval training and health in cancer survivors

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001855213
Acronym
PEER
Enrollment
108
Registered
2018-11-14
Start date
2016-11-08
Completion date
2021-09-13
Last updated
2022-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The purpose of this study is to determine whether a structured peer support program can improve exercise adherence and health-outcomes in breast, prostate and colorectal cancer survivors. Who is it for? You may be eligible for this study if you are an adult with confirmed breast, prostate or colorectal cancer, and are at least one month post-treatment completion for cancer. Study details All participants will undertake an initial 4-week supervised training phase, with 3 sessions per week of exercise with an accredited exercise physiologist or equivalent. Following the supervised phase, participants will enter a 1-year maintenance period where they will be asked to maintain 150 minutes of moderate intensity or 75 minutes of vigorous intensity or a combination, therefore meeting the Australian exercise oncology guidelines. Participants will be randomly assigned to either receive peer support or no peer support during the maintenance phase. It is hoped that this research will help determine if a peer support program is effective in enhancing exercise adherence and long-term health outcomes in cancer survivors.

Interventions

Randomised controlled intervention will compare peer support versus no peer support. Prior to randomisation all participants will complete a 4-week training program, supervised by an Accredited Exercise Physiologist or equivalent. This initial program required 3 times per week using a high-intensity interval training protocol of 4x4min intervals at 85-95% HRpeak, with 3 minute active recovery bouts in between. This protocol is a total of 38 minutes in duration. The purpose of this period is to e

Randomised controlled intervention will compare peer support versus no peer support. Prior to randomisation all participants will complete a 4-week training program, supervised by an Accredited Exercise Physiologist or equivalent. This initial program required 3 times per week using a high-intensity interval training protocol of 4x4min intervals at 85-95% HRpeak, with 3 minute active recovery bouts in between. This protocol is a total of 38 minutes in duration. The purpose of this period is to ensure all participants understand the exercise protocol and are able to complete it safely during the maintenance phase. Participants will then be randomised. Participants whom receive peer support will be paired with a peer supporter (a breast, prostate or colorectal cancer survivor) who have undergone training to provide specific support to their peers in the respect of building motivation, enhancing confidence and knowledge of practice and facilitating the enhancement of self-efficacy. This training is provided by Cancer Council Queensland's peer support team, whom have a program targeted at teaching 'how to peer support', specific for cancer patients and survivors. This training will be a 1-day long training. Peer supporters will provide support to their partner 3 times per week for a 12-month period. Peer supporters will be asked to contact their participant at least once per week face-to-face, with additional support provided by either phone, email, text or an additional face-to-face contact. There is no minimum requirements for how detailed these 3 contacts must be; however, peer supporters will keep a log of the date and type of contact given to their participant. Participants will be recruitment from the Brisbane area, with the intervention being run from the University of Queensland and partnered gyms in the wider Brisbane area.

Sponsors

The University of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

- Histologically confirmed breast, prostate and colorectal cancer - Aged 18 years or older - At least one-month post-cancer treatments and not intending undergoing any further treatment during the study period - Free of any musculoskeletal, neurological, respiratory, metabolic or cardiovascular conditions that may prevent safe completion of the exercise demands of the study

Exclusion criteria

- Currently performing >4 x/ month high intensity interval training - Unable to travel to the training/ testing facilities - Unable to give informed consent - Participant is pregnant or becomes pregnant during the study period

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026