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Feasibility of an 8-week Tai Chi Chuan Intervention for Breast Cancer Survivors

Primary Purpose

Cancer, Breast, Cognitive Impairment

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tai Chi
Sponsored by
UNC Lineberger Comprehensive Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Cancer, Breast

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Was diagnosed with breast cancer (all stages accepted).
  • Currently > 18 years of age
  • Age at cancer diagnosis > 18 years.
  • Able to engage in moderate intensity exercise as determined by their treating physician. If participant no longer has a treating physician, safety will be determined by following the American College of Sports Medicine (PAR-Q & YOU) physical activity questionnaire. An answer of "yes" to > one of the seven questions will require the participant to receive written permission from their physician prior to beginning the Tai Chi intervention.
  • Not previously engaged in regular exercise training (>1-2d/wk for >30 min/d) in past 6 months.
  • Completed chemotherapy treatment for a breast cancer diagnosis.
  • Cancer chemotherapy treatment completed within last 60 months. Defined as not currently scheduled for or undergoing active treatment (chemotherapy, radiation, surgery). Treatments to prevent or delay recurrence (e.g., breast cancer hormonal therapies) or for maintenance of remission are allowed.
  • Report experiencing cognitive impairment following treatment for cancer.
  • No psychiatric disorder with psychotic features.
  • Able to receive emails from study staff (i.e. for receiving study reminders).
  • Able to speak and read English.
  • Able to provide informed consent.

Exclusion Criteria:

  • Unwilling or unable to complete study procedures.
  • Currently participating in another study which would preclude participation in this study.
  • Has a known additional malignancy that is metastatic, progressing, or requires active treatment.
  • Has a neurocognitive disorder of other etiologies, such as Alzheimer's Parkinson's, etc., that might confound the analysis

Sites / Locations

  • UNC Chapel Hill Program on Integrative Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tai Chi

Arm Description

The Tai Chi intervention will be lead by an expert Tai Chi instructor with 15 years of teaching experience, and will take place at a local Yoga studio. The 8-week intervention entails two 75-minute sessions per week for a total of 16 sessions. Each session will begin with a 15- minute warm-up followed by 25 minutes of performing basic stances, footwork, upper-body/arm/hand movement, proper body alignment, mental/visual focus, and balance; 30 minutes of instruction in a choreographed form (first section of the Yang style long-form); and ending with a 5-minute cool-down.

Outcomes

Primary Outcome Measures

Feasibility - Attendance
Feasibility will be achieved if we observe at least 80% attendance (i.e., at least 13 out of 16 sessions attended).
Feasibility Pre-Test Completion
Feasibility will be achieved if we observe at least 80% completion. Completion rates will be the proportion of completed measures (number completed measures/total administered measures at pre-test).
Feasibility Post-Test Completion
Feasibility will be achieved if we observe at least 80% completion. Completion rates will be the proportion of completed measures (number completed measures/total administered measures at post-test).

Secondary Outcome Measures

Recruitment - Frequency Approached for Screening
We will describe the frequency approached for screening.
Recruitment - Proportion of Completed Screening
We will describe the proportion of completed screening (out of approached for screening)
Recruitment - Screened Eligible
We will describe those screened and found to be eligible (out of total screened).
Retention Rate
We will describe study retention (number who remain enrolled over 8 weeks/total number originally enrolled).
Recruitment - Enrollment Refusal
We will collect reasons for enrollment refusal (as part of the screening survey)
Retention - Withdrawals
We will collect reasons for study withdrawals.
Feasibility of the Different Recruitment Strategies - Screened
For each recruitment strategy, we will describe the frequency screened,
Feasibility of the Different Recruitment Strategies - Screened Eligible
For each recruitment strategy, we will describe those screened and found to be eligible (out of total screened).
Feasibility of the Different Recruitment Strategies - Enrolled
For each recruitment strategy, we will describe those enrolled (out of total screened eligible).
Expectancy/Credibility
The Expectancy/Credibility Questionnaire will be used to assess baseline expectancy and credibility effects of taking part in the Tai Chi intervention. Responses to six questions will be indicated with a 1 to 9 Likert-type scale, with higher numbers representing greater expectancy/credibility.
Acceptability
The Intervention Satisfaction Scale questions: 1) "Overall, I really enjoyed the Tai Chi intervention" and 2) "I would recommend the Tai Chi intervention to other cancer survivors" will assess acceptability. Acceptability will be achieved if the mean score is 3 or greater (response range: 0=Strongly disagree to 4=Strongly agree).
Intervention Satisfaction Questionnaire
Three close-ended questions will use a Likert scale (0= strongly disagree to 4=strongly agree) to assess whether the class length, frequency, and duration was satisfactory. Four open-ended questions will collect information on what participants liked or disliked about the Tai Chi intervention, and recommendations for changes to better address cancer survivors' needs and basic study procedures.

Full Information

First Posted
June 20, 2017
Last Updated
March 5, 2019
Sponsor
UNC Lineberger Comprehensive Cancer Center
Collaborators
North Carolina Translational and Clinical Sciences Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03196037
Brief Title
Feasibility of an 8-week Tai Chi Chuan Intervention for Breast Cancer Survivors
Official Title
Feasibility of an 8-week Tai Chi Chuan Intervention for Breast Cancer Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
December 5, 2017 (Actual)
Primary Completion Date
December 7, 2018 (Actual)
Study Completion Date
December 7, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
UNC Lineberger Comprehensive Cancer Center
Collaborators
North Carolina Translational and Clinical Sciences Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Purpose:To gather preliminary data and to determine the feasibility and acceptability of an 8-week Tai Chi intervention for adults cancer survivors (survivors) who report experiencing cognitive impairment, and to perform exploratory analyses to assess improvements in cognitive performance, health-related quality of life, brain activity, and blood-based biomarkers. Participants: Adult survivors (> 18 years old) who report experiencing cognitive impairment and are within 60 months of completion of chemotherapy for treatment of a breast cancer diagnosis. Procedures (methods): A single arm pre-/post-test non-randomized study design in adult cancer survivors (Enrollment goal N=15; current age ≥ 18 years, treatment completed within 60 months). Outcomes will be assessed at baseline and after the 8-week Tai Chi intervention, and consist of feasibility, acceptability, expectancy/credibility, health-related quality of life, cognitive performance, serum biomarkers, and brain activity.
Detailed Description
The objective of this study is to gather preliminary data and to determine the feasibility and acceptability of an 8-week Tai Chi intervention for adults within 60 months of having completed chemotherapy for treatment of a cancer diagnosis who report experiencing cognitive impairment (cancer-related cognitive impairment; CRCI). Tai Chi is a form of physical activity that includes an inherent level of cognitive engagement into its performance. Rodent studies provide evidence that including a cognitive component to physical activity (PA) changes its effect on the brain, with aerobic PA inducing angiogenesis and cognitively engaging PA inducing synaptogenesis. Human research with older adults indicates that interventions that combine PA and cognitive engagement produce greater cognitive benefits than PA alone. Experimental and meta-analytic evidence have shown that participation in PA improves cognitive performance in nonclinical and clinical populations, including breast cancer survivors. Importantly, physical activity benefits the same cognitive domains that are negatively affected by CRCI (i.e., attention/processing, memory, executive function). Recently, meta-analytic evidence showed that PA might benefit CRCI. However, in most studies cognitive outcomes are limited to measures of subjective cognitive function rather than objective measures of performance such as neuropsychological assessments or brain activity (e.g., EEG). Research into the effects of Tai Chi on CRCI is sparse, yet promising. Additionally, research has shown positive effects from Tai Chi on health-related quality of life and cytokines in cancer survivors. To achieve our objective of examining feasibility and acceptability of an 8-week Tai Chi intervention, we will use a single arm pre-/post-test non-randomized study design in adult breast cancer survivors (Enrollment goal N=15; current age ≥ 18 years, treatment completed within 60 months). Outcomes will be assessed at baseline and after the 8-week Tai Chi intervention, and consist of feasibility, acceptability, expectancy/credibility, health-related quality of life, cognitive performance, serum biomarkers, and brain activity. This feasibility study will help identify barriers to recruitment and retention, determine the acceptability of a 8- week Tai Chi intervention for cancer survivors, and provide data for use in designing subsequent studies. Specifically, the findings will inform the design of a randomized controlled trial (RCT) that is sufficiently powered to examine efficacy. The ultimate goal of this research is to create and test a method of investigation into the use of Tai Chi to prevent or mitigate CRCI as well as a method of improving health-related quality of life in cancer survivors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Breast, Cognitive Impairment

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A single-arm pre-/post-test non-randomized study design.
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tai Chi
Arm Type
Experimental
Arm Description
The Tai Chi intervention will be lead by an expert Tai Chi instructor with 15 years of teaching experience, and will take place at a local Yoga studio. The 8-week intervention entails two 75-minute sessions per week for a total of 16 sessions. Each session will begin with a 15- minute warm-up followed by 25 minutes of performing basic stances, footwork, upper-body/arm/hand movement, proper body alignment, mental/visual focus, and balance; 30 minutes of instruction in a choreographed form (first section of the Yang style long-form); and ending with a 5-minute cool-down.
Intervention Type
Behavioral
Intervention Name(s)
Tai Chi
Intervention Description
An 8-week Tai Chi intervention consisting of 75-minute group sessions held twice a week, over 8 weeks (i.e., total of 16 sessions).
Primary Outcome Measure Information:
Title
Feasibility - Attendance
Description
Feasibility will be achieved if we observe at least 80% attendance (i.e., at least 13 out of 16 sessions attended).
Time Frame
post 8-week intervention
Title
Feasibility Pre-Test Completion
Description
Feasibility will be achieved if we observe at least 80% completion. Completion rates will be the proportion of completed measures (number completed measures/total administered measures at pre-test).
Time Frame
Baseline
Title
Feasibility Post-Test Completion
Description
Feasibility will be achieved if we observe at least 80% completion. Completion rates will be the proportion of completed measures (number completed measures/total administered measures at post-test).
Time Frame
post 8-week intervention
Secondary Outcome Measure Information:
Title
Recruitment - Frequency Approached for Screening
Description
We will describe the frequency approached for screening.
Time Frame
Baseline
Title
Recruitment - Proportion of Completed Screening
Description
We will describe the proportion of completed screening (out of approached for screening)
Time Frame
Baseline
Title
Recruitment - Screened Eligible
Description
We will describe those screened and found to be eligible (out of total screened).
Time Frame
Baseline
Title
Retention Rate
Description
We will describe study retention (number who remain enrolled over 8 weeks/total number originally enrolled).
Time Frame
post 8-week intervention
Title
Recruitment - Enrollment Refusal
Description
We will collect reasons for enrollment refusal (as part of the screening survey)
Time Frame
Baseline
Title
Retention - Withdrawals
Description
We will collect reasons for study withdrawals.
Time Frame
post 8-week intervention
Title
Feasibility of the Different Recruitment Strategies - Screened
Description
For each recruitment strategy, we will describe the frequency screened,
Time Frame
Baseline
Title
Feasibility of the Different Recruitment Strategies - Screened Eligible
Description
For each recruitment strategy, we will describe those screened and found to be eligible (out of total screened).
Time Frame
Baseline
Title
Feasibility of the Different Recruitment Strategies - Enrolled
Description
For each recruitment strategy, we will describe those enrolled (out of total screened eligible).
Time Frame
Baseline
Title
Expectancy/Credibility
Description
The Expectancy/Credibility Questionnaire will be used to assess baseline expectancy and credibility effects of taking part in the Tai Chi intervention. Responses to six questions will be indicated with a 1 to 9 Likert-type scale, with higher numbers representing greater expectancy/credibility.
Time Frame
Baseline
Title
Acceptability
Description
The Intervention Satisfaction Scale questions: 1) "Overall, I really enjoyed the Tai Chi intervention" and 2) "I would recommend the Tai Chi intervention to other cancer survivors" will assess acceptability. Acceptability will be achieved if the mean score is 3 or greater (response range: 0=Strongly disagree to 4=Strongly agree).
Time Frame
post 8-week intervention
Title
Intervention Satisfaction Questionnaire
Description
Three close-ended questions will use a Likert scale (0= strongly disagree to 4=strongly agree) to assess whether the class length, frequency, and duration was satisfactory. Four open-ended questions will collect information on what participants liked or disliked about the Tai Chi intervention, and recommendations for changes to better address cancer survivors' needs and basic study procedures.
Time Frame
post 8-week intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Was diagnosed with breast cancer (all stages accepted). Currently > 18 years of age Age at cancer diagnosis > 18 years. Able to engage in moderate intensity exercise as determined by their treating physician. If participant no longer has a treating physician, safety will be determined by following the American College of Sports Medicine (PAR-Q & YOU) physical activity questionnaire. An answer of "yes" to > one of the seven questions will require the participant to receive written permission from their physician prior to beginning the Tai Chi intervention. Not previously engaged in regular exercise training (>1-2d/wk for >30 min/d) in past 6 months. Completed chemotherapy treatment for a breast cancer diagnosis. Cancer chemotherapy treatment completed within last 60 months. Defined as not currently scheduled for or undergoing active treatment (chemotherapy, radiation, surgery). Treatments to prevent or delay recurrence (e.g., breast cancer hormonal therapies) or for maintenance of remission are allowed. Report experiencing cognitive impairment following treatment for cancer. No psychiatric disorder with psychotic features. Able to receive emails from study staff (i.e. for receiving study reminders). Able to speak and read English. Able to provide informed consent. Exclusion Criteria: Unwilling or unable to complete study procedures. Currently participating in another study which would preclude participation in this study. Has a known additional malignancy that is metastatic, progressing, or requires active treatment. Has a neurocognitive disorder of other etiologies, such as Alzheimer's Parkinson's, etc., that might confound the analysis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aaron T Piepmeier, PhD
Organizational Affiliation
University of Rhode Island
Official's Role
Study Director
Facility Information:
Facility Name
UNC Chapel Hill Program on Integrative Medicine
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599-7200
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plan.

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Feasibility of an 8-week Tai Chi Chuan Intervention for Breast Cancer Survivors

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