Optimizing Functional Recovery After Breast Cancer Treatment

Summary

The goal of this clinical trial is to determine the best way to promote participation in vocational, social, physical, and instrumental activities of daily living in people who have completed treatment for early stage breast cancer.

The main question it aims to answer is: Which of the intervention components, alone or in combination, most effectively promote participation in vocational, social, physical, and instrumental activities of daily living?

Participants will be asked to try one of 8 combination of three intervention components that have been shown to promote activity participation: (1) priority elicitation, (2) education, and (3) guided application involving goal setting, problem-solving and action planning.

Conditions

• Breast Neoplasms

Interventions

BEHAVIORAL

Individually tailored education and guided application to promote activity participation

This condition has high levels of the three components: (1) priority-elicitation and session tailoring; (2) cancer survivorship education; and (3) guided application involving goal setting, problem-solving, and action planning.

BEHAVIORAL

Individually tailored guided application

This condition contains high levels of priority elicitation and guided application.

BEHAVIORAL

Individually tailored education

This condition contains how levels of the components of priority elicitation and education

BEHAVIORAL

Priority elicitation

This condition contains the high level of the priority elicitation component

BEHAVIORAL

Static education and guided application

This condition has high levels of the education and guided application components

BEHAVIORAL

Static guided application

This condition contains high level of the guided application component

BEHAVIORAL

Static education

This condition contains the high level of the education component

BEHAVIORAL

Information

This condition contains the low levels of the three components

Sponsors & Collaborators

• University of Alabama at Birmingham

  collaborator OTHER

• University of South Alabama

  collaborator OTHER

• Dartmouth-Hitchcock Medical Center

  collaborator OTHER

• MGH Institute of Health Professions

  lead OTHER

Principal Investigators

• Kathleen D Lyons, ScD · MGH Institute of Health Professions

Study Design

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

DOUBLE

Model

FACTORIAL

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2027-01-01

Primary Completion

2030-09-30

Completion

2030-09-30

Countries

• United States

Study Locations