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Clinical Trials/NCT03702712
NCT03702712
Completed
Not Applicable

Acute Effects of Aerobic Exercise and Relaxation on Fatigue and Executive Function in Breast Cancer Survivors

University of Illinois at Urbana-Champaign1 site in 1 country40 target enrollmentOctober 15, 2018
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
University of Illinois at Urbana-Champaign
Enrollment
40
Locations
1
Primary Endpoint
Piper Fatigue Scale
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this acute study is to compare the combined effects of aerobic exercise and relaxation training on fatigue and its related cognitive components, among breast cancer survivors. Participants will complete three sessions over a seven-day period in a laboratory setting.

Detailed Description

It is hypothesized that the combination of aerobic exercise and relaxation training could have additive effects on fatigue and related cognitive outcomes. Therefore, this study is designed to test the effects of exercise plus relaxation relative to aerobic exercise alone and relaxation training alone, over the course of three sessions within a seven day period. Participants will complete baseline and post-testing before and after the week of training, as well as pre- and post-testing at each session. Participants will be randomized to one of three conditions: 1. Aerobic Exercise Only Condition (AERO) Participants randomized to the AERO condition will engage in three separate 20-minute sessions comprised of a 5-minute, resistance-free warm-up, and 15 minutes of moderate aerobic cycling on a stationary bike (50-70% age-predicted heart rate max). Each AERO session will end with a 20-minute quiet rest period. 2. Relaxation Only Condition (RELAX) Participants in the RELAX condition will complete three separate 20-minute sessions of relaxation training using a commercial neurofeedback device (headset \& smartphone app). Each RELAX session will end with a 20-minute quiet rest period. 3. Aerobic Exercise and Relaxation Training - Intervention Condition (COMBINED) Participants randomized to the COMBINED condition will complete three separate sessions comprised of 20 minutes of AERO exercise followed by 20 minutes of RELAX training. All participants, regardless of condition will complete brief questionnaires assessing in-the-moment fatigue and affect, before and after each randomly assigned activity session. A larger survey and battery of cognitive tests will be completed at the beginning of the first appointment and at the conclusion of the third appointment.

Registry
clinicaltrials.gov
Start Date
October 15, 2018
End Date
February 28, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sean Mullen

Associate Professor

University of Illinois at Urbana-Champaign

Eligibility Criteria

Inclusion Criteria

  • 18 years and older
  • previously diagnosed with breast cancer (ductal carcinoma in situ or stages I-IV)
  • completed at least one cycle of chemotherapy treatment within the last 5 years
  • must have reliable access to the internet
  • must report at least one complaint concerning physical function, fatigue, memory, planning, thinking, negative mood, depressive symptoms, or anxiety
  • must be capable of engaging in sustained stationary cycling at a moderate intensity

Exclusion Criteria

  • deaf in both ears
  • unable to comfortably wear a pair of ear-bud headphones
  • color-blind or do not have vision of at least 20/40 with the aid of contacts or glasses
  • history or diagnosis of epilepsy

Outcomes

Primary Outcomes

Piper Fatigue Scale

Time Frame: This will be assessed on day 1 (baseline), day 2 and day 3 (post-testing), both before and after randomized activities.

The Piper Fatigue Scale requires respondents to select their answers according to a "0" (most positive or desirable response) to "10" (most negative, fatigue is having a strong impact) scale. A total fatigue score is calculated by summing each of the 12 responses and dividing by 12. Accordingly, a total fatigue change score of 0 corresponds to no fatigue, a score of 1-3 is labeled as mild, 4-6 is labeled as moderate, and 7-10 is labeled as severe. The total scores from each of the three days will be used to calculate an overall fatigue score, which will be used to assess group level differences across averages. Our operational definition of overall fatigue in this outcome is the average score across each group.

Secondary Outcomes

  • Perceived Mental Fatigue(The PMFQ will be assessed on day 1 (baseline), day 2, and day 3 (post-testing).)
  • Energy subscale of AD ACL-SAI(This will be assessed following randomized activities on Day 1 (baseline), Day 2, and Day 3 (post-testing).)
  • Tiredness subscale of AD ACL-SAI(This will be assessed following randomized activities on Day 1 (baseline), Day 2, and Day 3 (post-testing).)
  • Attention- Assessed by Flanker Inhibitory Control and Attention task from the NIH toolbox(This will be assessed prior to randomized activities on day 1 (baseline), and day 3 (post-testing))
  • Working Memory- Assessed by Picture Sequence task from the NIH toolbox(This will be assessed prior to randomized activities on day 1 (baseline), and day 3 (post-testing))
  • Cognitive Flexibility and Attention- Assessed by Dimensional Change Card Sort Task from the NIH toolbox(This will be assessed prior to randomized activities on day 1 (baseline), and day 3 (post-testing))
  • Program Evaluation - Perceived Usefulness(This will be assessed on day 3.)
  • Program Evaluation - Perceived Ease of Use(This will be assessed on day 3.)
  • Program Evaluation - Enjoyment(This will be assessed on day 3.)
  • Program Evaluation - Satisfaction(This will be assessed on day 3.)
  • Program Evaluation - Open Ended(This will be assessed on day 3.- focusing on thoughts of the program over the three appointment days, in a 1-week period.)

Study Sites (1)

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