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Supporting cancer survivors to stand up, sit less and move more

A pilot study of a text message intervention to improve whole-of-day activity in cancer survivors participating in clinical exercise rehabilitation

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000641493
Enrollment
38
Registered
2016-05-17
Start date
2016-03-15
Completion date
2016-04-26
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This pilot randomised controlled trial aims to develop and evaluate an innovative intervention to reduce sitting and improve activity in cancer survivors participating in clinical exercise rehabilitation. In addition to participating in the 4-week exercise clinic (1 1h session per week), half of the participants will be randomly allocated to also receive a text messaging intervention to support behaviour change outside of the face to face clinic. The 3-month intervention will consist of a suite of text messages tailored through coaching sessions conducted at baseline and 4-weeks. The primary outcome is overall sitting time (h/day) measured y the activPAL3 activity monitor. Secondary outcomes include standing time and stepping time, use of time and key clinical outcomes measured using the activPAL3, the Multimedia Activity Recall for Children and Adults (MARCA), and a clinical assessment battery, respectively. All outcomes will be measured at baseline, 4-weeks and 12-weeks. Feasibility and acceptability will also be assessed. It is hypothesised that the intervention will reduce sitting time in intervention participants compared to those that receive the exercise clinic only.

Interventions

All participants will attend a 4-week exercise clinic for cancer surivors. Participation in the exercise clinic is optional for people with a previous diagnosis of cancer. Participants will be prescribed 1 h, individualized, supervised exercise sessions once weekly for 4 weeks. Participants will be encouraged to increase their physical activity levels outside of the exercise sessions. All testing and training sessions will be conducted in the School of Human Movement and Nutrition Sciences Gymna

All participants will attend a 4-week exercise clinic for cancer surivors. Participation in the exercise clinic is optional for people with a previous diagnosis of cancer. Participants will be prescribed 1 h, individualized, supervised exercise sessions once weekly for 4 weeks. Participants will be encouraged to increase their physical activity levels outside of the exercise sessions. All testing and training sessions will be conducted in the School of Human Movement and Nutrition Sciences Gymnasium. Participants are individually supervised (see below) in groups of up to 10 participants. Participants will complete sessions prescribed by final year clinical exercise physiology students in a 2:1 student:participant ratio supervised by Accredited Exercise Physiologists in a 1:2 AEP:participant ratio. The exercise program will be individualized to address participant goals, preferences, medical history and initial assessment results. Each 1 h session included: low intensity aerobic warm-up (5–10 min); four to six progressive upper and lower body resistance exercises of 10–12RM (targeting the chest, biceps, triceps, quadriceps, hamstrings and latissimus dorsi muscle groups) using machine, free weights and/or resistance bands; balance activities; low intensity aerobic cool down (5–10 min); static muscle stretching activities; and education on the benefits of exercise for health. Resistance load was increased by 5–10 percent when participants exceeded the prescribed RM. Accredited exercise physiologists will record attendance and any adverse (i.e. any untoward medical occurrence occurring during the exercise sessions), or serious adverse events (i.e. adverse events that are still ongoing at the end of the study period). In addition to participating in the 4-week exercise clinic, half of the participants will be randomly allocated to receive a text messaging intervention that will commence at the same time as the clinic. The 3-month intervention consists of a suite of text messages tailored through coaching sessions that draw on participants' activity data. Participants receive a minimum of 4 text messages per fortnight that will target: reducing overall sedentary time, breaking up prolonged periods (30 mins+) of sedentary time with light intensity activities (including standing), and increasing MVPA. The text messaging intervention will begin with a face-to-face, one-on-one coaching session (approx. 30 minutes duration conducted at the university) to: 1) orientate the participant to the ‘whole-of-day’ approach; and, 2) collect information to tailor the text message content and timing. Participants’ baseline activity data will be used by the coach to guide participants to identify goals and strategies for changing their daily activities. Following the initial coaching session, each intervention participant will be sent a minimum of four tailored text messages per fortnight for the 12-week period, with more frequent texts able to be provided at the request of the participant. The text messages will target: 1) education (overall and prolonged sitting and MVPA); 2) real time prompting (prolonged sitting and MVPA); and, 3) goal checking (MVPA). Intervention participants will engage in another face-to-face coaching session after the 4-week Exercise Clinic (approx. 30 minutes duration) to update their preferences for text message content and timing. All coaching sessions will be conducted by a qualified health professional (e.g. Exercise Physiologist/Physiotherapist). Attendance at coaching sessions will be recorded. The participants are not required to wear any monitoring devices throughout the intervention other than that described in the outcome measures.

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

Participants have to opt in to the exercise clinic in order to be eligible for this study. articipation in the exercise clinic is optional for people with a previous diagnosis of cancer. To be included in the study, participants will have a previous diagnosis of cancer (excluding childhood cancers) and be at least one-month post surgery, with relevant information obtained from their medical practitioner (e.g. comorbidities, injuries, medications) to assist with exercise testing and prescription. Participants must also own a mobile phone.

Exclusion criteria

Participants will be excluded if they have established metastatic bone disease, or cardiopulmonary or metabolic disorders that will prevent safe participation in the testing or exercise sessions.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 2, 2026