Recruiting

Habit-Based Program

Sponsor:

University of Toronto

Code:

NCT07694479

Conditions

Cancer

Sedentary Behaviour

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Sedentary Behaviour Intervention

Active Control Group

Study Details

Brief summary:

Cancer and its treatments are associated with long-term side effects including lowered physical strength and quality of life. Decreasing sedentary behaviour improves health outcomes in cancer survivors. Habit-based programs aimed at lowering sedentary behaviour have been successful in decreasing sedentary behaviour in other populations. However, limited clinical trials aimed at lowering sedentary behaviour have recruited cancer survivors, and none are exclusively based on Habit Theory.

The primary goal of this clinical trial is to test the feasibility of an 8-week, habit-based program to lower sedentary behaviour in cancer survivors. Sedentary behaviour refers to low-energy activities performed during waking hours in a seated, reclined or laid down position. Secondarily, this clinical trial aims to examine changes in sedentary behaviour, physical strength, habit, and quality of life.

Enrolled participants will be assigned to a sedentary behaviour or active control group. The sedentary behaviour group will receive 8 weekly sheets consisting of tips recommending to lower sedentary behaviour. Tips will be individualized to participants' lifestyles, and will consider their cancer-specific and other physical limitations. Participants in the sedentary behaviour group will also meet with the researcher once a week for a check-in session for more individualized tips and progressions. The active control group will receive the Canadian 24-hour Movement Guidelines, and a handout highlighting the benefits of lowering sedentary behaviour. Both groups will be provided with wearable activity monitors (Fitbits).

Conditions

Cancer

Sedentary Behaviour

Study ID

NCT07694479

Start date

Dec 30, 2025

Status verified date

Jul, 2026

Completion date

Sep, 2026

Anticipated

Primary completion date

Sep, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 18 years of age or older
  • have been diagnosed with localized or asymptomatic metastatic cancer of any type
  • completed primary cancer treatment
  • self-report being sedentary for more than or equal to 8 hours per day
  • access to the internet and a device with a webcam
  • able to complete the study in English

Exclusion Criteria:

  • presence of other primary or recurrent invasive cancer
  • having experienced a fall in the last 12 months
  • not residing in Canada
  • participating in other behaviour change interventions
  • using a gait aid device

Study Design

Enrollment

30 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Sedentary Behaviour Intervention Group

The sedentary behaviour intervention will consist of weekly tick-sheets, one weekly check-in session, and a Fitbit for physical inactivity reminders over 8 weeks. The weekly tick-sheets will consist of tips recommending to lower sedentary behaviour by enacting actions in the presence of cues. Progressions, illustrations and steps to perform these actions will be provided as an attachment with the tick-sheets. An example of a tip is "During TV/online video ad breaks or when you finish watching one episode of a show or online video, climb up and down a staircase to reduce cancer-related fatigue associated with prolonged sitting". Tips will be individualized to participants' lifestyles, and will consider their cancer-specific and other physical limitations. Participants in the sedentary behaviour group will also meet with the researcher once a week for a check-in session for more individualized tips and progressions.

active comparator: Active Control Group

The active control group will receive the Canadian 24-hour Movement Guidelines, and a handout highlighting the benefits of reducing sedentary behaviour. They will also receive Fitbits, with the hourly inactivity reminders turned off.

Interventions

Sedentary Behaviour Intervention

The sedentary behaviour intervention will consist of weekly tick-sheets, one weekly check-in session, and a Fitbit for physical inactivity reminders over 8 weeks. The weekly tick-sheets will consist of tips recommending to lower sedentary behaviour by enacting actions in the presence of cues. Progressions, illustrations and steps to perform these actions will be provided as an attachment with the tick-sheets. An example of a tip is "During TV/online video ad breaks or when you finish watching one episode of a show or online video, climb up and down a staircase to reduce cancer-related fatigue associated with prolonged sitting". Tips will be individualized to participants' lifestyles, and will consider their cancer-specific and other physical limitations. Participants in the sedentary behaviour group will also meet with the researcher once a week for a check-in session for more individualized tips and progressions.

Active Control Group

The active control group will receive the Canadian 24-hour Movement Guidelines, and a handout highlighting the benefits of reducing sedentary behaviour. They will also receive Fitbits, with the hourly inactivity reminders turned off.

Primary outcome measure

  • Enrollment [ Time Frame: Change from baseline (pre- intervention) to post-intervention (8 weeks). ]
  • Adherence [ Time Frame: From baseline (pre-intervention) to post-intervention (8 weeks). ]
  • Attrition [ Time Frame: Assessed from baseline (pre-intervention) to post-intervention (8 weeks). ]
  • Adverse Events [ Time Frame: From baseline (pre-intervention) to post-intervention (8 weeks). ]
  • Participant Satisfaction [ Time Frame: Post-intervention (8 weeks). ]

Central Contacts and Locations

Locations

University of Toronto - Athletic Centre

Recruiting

Toronto, Ontario, Canada, M5S 2W6

Contacts

Principal Investigator:

Deema Khalaf, BSc

More Information

Sponsor

University of Toronto

Last update posted

Jul 10, 2026

Last verified

Jul, 2026

Keywords

  • cancer survivorship
  • quality of life
  • physical function
  • cancer
  • remote delivery
  • feasibility
  • sedentary behaviour intervention

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Toronto on 2026-07-10.