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Step by Step: A Tailored Walking Intervention for Breast Cancer Survivors

Feasibility of a Technology-based Intervention to Reach Inactive Breast Cancer Survivors and Objectively Track Step Activity.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01845519
Enrollment
90
Registered
2013-05-03
Start date
2013-07-31
Completion date
2014-06-30
Last updated
2015-06-01

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

Conditions

Breast Neoplasms, Sedentary Lifestyle, Survival Rate (Survivorship)

Brief summary

This study aims to recruit post-treatment breast cancer survivors for a 12-week 2-arm randomized walking intervention. All intervention materials will be delivered electronically. The investigators hypothesize that at the end of 12-weeks, participants randomized to the intervention group will engage in more weekly steps than those participants randomized to the comparison group.

Detailed description

More than two-thirds of breast cancer survivors are physically inactive. Inactivity is known to negatively impact both morbidity and mortality, and is especially pronounced among cancer survivors. Self-directed interventions targeting inactivity among breast cancer survivors often report clinically insignificant behavior change. More successful behavior change interventions have suggested that tailoring and, more recently, the fostering of intrinsic motivation, may have improved outcomes. However, no interventions to date have utilized these approaches to increase physical activity among sedentary cancer survivors. AIM 1: Develop and test intervention (tailored) and comparison group (targeted) messages in a sample of sedentary women to determine message acceptability. AIM 2: Determine the efficacy of a 12-week tailored intervention to increase the number of weekly steps taken among sedentary post-treatment breast cancer survivors compared to a 12-week, targeted intervention.

Interventions

BEHAVIORALTailored Email

Participants will receive tailored emails.

BEHAVIORALTargeted Email

Participants will receive targeted emails.

Sponsors

UNC Lineberger Comprehensive Cancer Center
CollaboratorOTHER
University of North Carolina
CollaboratorOTHER
Leanne Kaye
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Female * 40-70 years of age * History of breast cancer stage I-II * 2-10 years post-treatment * Sedentary * Technology access and skills * Regular access to personal computer/ broadband internet and email account * Comfortability using internet, and web-based tools * US Resident

Exclusion criteria

* Concurrent enrollment in another physical activity/ lifestyle/ weight loss intervention program/study * Current secondary cancer diagnosis/ treatment * Inability to ambulate * Refusal to wear personal activity monitor (FitBit Ultra) for the duration of the study * Engaging in regular moderate to vigorous physical activity

Design outcomes

Primary

MeasureTime frameDescription
Difference in weekly steps between intervention and comparison group at the end of the intervention (week 12).12 weeksThe primary outcome will be measured using weekly step data as measured by a commercially available accelerometer. The primary outcome will be the difference in weekly steps between the intervention and comparison group at the end of the intervention (week 12).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026