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

L

Leanne Kaye

Status

Completed

Conditions

Survival Rate (Survivorship)
Breast Neoplasms
Sedentary Lifestyle

Treatments

Behavioral: Targeted Email
Behavioral: Tailored Email

Study type

Interventional

Funder types

Other

Identifiers

NCT01845519
IRB 121775

Details and patient eligibility

About

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.

Full 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.

Enrollment

90 patients

Sex

Female

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

90 participants in 2 patient groups

Tailored Group
Experimental group
Treatment:
Behavioral: Tailored Email
Targeted Group
Active Comparator group
Treatment:
Behavioral: Targeted Email

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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