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Feasibility Study of the Addition of a Personal Trainer to the Post-Treatment Regimen of Breast Cancer Survivors

Feasibility Study of the Addition of a Personal Trainer to the Post-Treatment Regimen of Breast Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02770781
Enrollment
68
Registered
2016-05-12
Start date
2015-10-31
Completion date
2018-07-11
Last updated
2019-04-09

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

Conditions

Breast Cancer

Keywords

survivors, physical fitness

Brief summary

The purpose is to examine the feasibility and preliminary effectiveness of the role of a personal trainer for non-metastatic breast cancer survivors to improve physical activity and well-being (in terms of quality of life).

Detailed description

After breast cancer treatment, many women are faced with effects of treatment such as changes in appearance, fatigue, and reduced quality of life as compared to the pre-disease state. An intervention to increase physical activity may be helpful to improve well-being and outcomes for women treated for breast cancer.

Interventions

Subjects will receive a personal exercise regimen based on their health history and individual capability.

Sponsors

University of Pittsburgh
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female * Post active breast cancer therapy (e.g. surgery and/or chemotherapy and/or radiation therapy), but may still be undergoing maintenance cancer therapy. * Free of macro-metastatic disease * Sedentary pre-cancer diagnosis: Those individuals not participating in a regular exercise program or not meeting the minimal physical activity recommendations from the General Surgeon which is accumulating 30 minutes or more of moderate physical activity on most days of the week * Ability to provide informed consent * Ability to provide a written physician's clearance * Patients must be new to the Survivorship Clinic (within first 12 months).

Exclusion criteria

* Medical conditions that would preclude participation in a weight-training program. * Those who plan on relocating outside the Greater Pittsburgh Area in the next 3 months of intervention.

Design outcomes

Primary

MeasureTime frameDescription
Study recruitment abilityBaseline through ~ 6 months of follow-up.Pilot study

Secondary

MeasureTime frameDescription
Physical fitnessBaseline through ~ 6 months of follow-up.Measured by pedometer.
Change in Paffenberger Exercise habits questionnaireBaseline and ~ 6 monthsThis questionnaire asks about exercise habits.
Change in physical activity self-efficacy questionnaireBaseline and ~ 6 monthsThis questionnaire will measure a person's perceived competence to engage in an activity
Functional Assessment of Cancer Therapy - Endocrine SymptomsBaseline and ~ 6 monthsThis is a quality of life questionnaire

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026