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Exercise Intervention for Cancer Survivors and Caregivers

NCT01883635 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2016-02-05

Study results available
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Summary

The purpose of the study is to see whether exercise can improve the health and well-being of cancer survivors. We also want to know about the health and well being of caregivers.

Conditions

Interventions

BEHAVIORAL

Survivor-only progressive walking and resistance exercise

Daily, home-based, tailored exercise program delivered over the course of 6 weeks to the survivor only

BEHAVIORAL

Dyadic progressive walking and resistance exercise

Daily, home-based, tailored exercise program delivered over the course of 6 weeks to the survivor and caregiver as a dyad

Sponsors & Collaborators

  • University of Rochester

    lead OTHER

Principal Investigators

  • Charles Kamen, PhD · University of Rochester

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2015-05-31
Completion
2015-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01883635 on ClinicalTrials.gov