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Increasing Physical Activity Among Breast Cancer Survivors With Depression

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Breast Cancer
Physical Activity
Depression

Treatments

Behavioral: Print-based education
Other: Facility Access
Device: Fitbit
Behavioral: Active Living counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT02781051
STU 122015-072

Details and patient eligibility

About

Pilot study to assess a multi-component intervention to increase physical activity among breast cancer survivors with depression.

Full description

The research project is a pilot study to assess the effects of a multi-component intervention in increasing physical activity among breast cancer survivors with depression. Individuals meeting inclusion/exclusion criteria will be enrolled in the 12-week intervention with a 6 month follow up. Intervention components will include print-based education, self-monitoring, Active Living counseling, and facility access. Blood samples will be collected at baseline. Assessments (anxiety, stress, sleep) and sample collection will also occur at 3 time points during the intervention (Weeks 7, 13, and 25). Changes in physical activity will be assessed using Fitbits to measure weekly minutes of moderate/vigorous activity.

Enrollment

16 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Positive depression screen (PHQ-9) or current antidepressant treatment
  • Report <150 minutes of weekly moderate-to-vigorous physical activity (MVPA) on the GPAQ
  • Physically able to engage in physical activity
  • Written and verbal fluency in English

Exclusion criteria

  • Medical condition contraindicating physical activity participation
  • Recurrence of breast cancer
  • Ductal carcinoma in situ (DCIS) diagnosis
  • Cognitively unable to give informed consent
  • Non-English speaking

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

16 participants in 1 patient group

Physical Activity Intervention
Experimental group
Description:
Participants will participate in a multi-component physical activity intervention for 12 weeks with a 6 month follow up.
Treatment:
Behavioral: Active Living counseling
Behavioral: Print-based education
Device: Fitbit
Other: Facility Access

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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