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Body Mind Training Project

Effects of Qigong on Fatigue & Quality of Life in Elderly Prostate Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01564394
Enrollment
60
Registered
2012-03-27
Start date
2011-10-31
Completion date
2012-09-30
Last updated
2015-12-08

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

Conditions

Cancer Related Fatigue

Keywords

qigong, mindfulness meditation, fatigue, prostate cancer

Brief summary

Aim 1: Assess the feasibility, safety and efficacy of a Qigong intervention in elderly prostate cancer survivors. Describe participation, retention, and adherence rates and assess reasons for participation, attrition, and non-adherence. Identify effective recruitment and retention strategies. Ascertain participants' level of satisfaction and additional perceptions of the experimental and control interventions, perceived study burden, study design, and implementation. Aim 2: Provide preliminary data on potential effects of Qigong vs. non-aerobic stretching exercises on fatigue, psychosocial outcomes, and health-related quality of life in preparation for a future R01 application for a larger, definitive randomized controlled trial. Hypothesis: Qigong participants will have improved fatigue levels, quality of life, and related psychosocial and health outcomes compared to those randomized to the non-aerobic stretching group.

Detailed description

This ongoing feasibility study is a two-armed, parallel group, randomized clinical trial.We will recruit 60 elderly prostate cancer survivors (age 55+ years) and their significant others (spouse, domestic partner, or close family member). Considering literature attesting to strains associated with caregiver status, we will also collect survey and physical assessment data to explore the intervention's effect on significant others. Recruitment occurs through Huntsman Cancer Institute's outpatient clinic and University and community-based strategies (for example, newspaper ads, flyers, support groups, patient registries). We will measure relevant psychosocial measures, including fatigue and quality of life (SF36 & EPIC), perceived stress, distress, mood, cognitive function, social connectedness, demographics, and leisure time, at baseline, the six-week midpoint, and one week post-intervention. Weekly measures of fatigue and quality of life and physical activity logs will also be administered. Biometric assessments, including balance and mobility, flexibility, blood pressure, resting heart rate, body mass index, and waist-hip-ratio, will be done at baseline (before randomization) and one week post-intervention. Significant others will undergo the same survey measures as the prostate cancer survivors, except for measures specific to prostate cancer (e.g., EPIC-26-short form). Participants will be recruited in two cohorts, one beginning early March and the other early June, 2012. The twice-weekly exercise classes will be 60 minutes in duration, running for 12 weeks. Classes will be conducted at Huntsman Cancer Institute's Survivor & Wellness Center, beginning one week after baseline physical assessments. Participants will receive a DVD of the respective class led by trained and qualified instructors so they can supplement classes with home-based sessions. Qigong class will consist of postures, movements, deep breathing techniques, and meditation, including an emphasis on weight shifting, breath, and posture control. Non-aerobic stretching will consist of light stretching exercises that avoid focus on meditation. This class will serve as the control group for non-specific factors such as attention dose and the group setting. To ensure consistency of physical intensity between the two study arms, both objective (heart rate monitors) and subjective (self-reported ten-point Borg scale) measures will be performed on participants.

Interventions

BEHAVIORALQigong

Classes will be 60 minutes in duration, held two times a week, supplemented with home-based sessions over 12 weeks. The classes will be led by a trained Qigong instructor and consist of postures, movements, deep breathing techniques and meditation. It will include eccentrically-biased Qigong movements with an emphasis on weight shifting and posture control. The continuous body movements coupled with progressively diminishing base of support, dynamic challenge to balance, and concentration on body positions requiring eccentric muscle activity should improve the levels of fatigue and quality of life in older prostate cancer survivors.

BEHAVIORALNon-aerobic stretching

The non-aerobic stretching classes will serve as an attention control. They will be 60 minutes in duration, held two times a week, supplemented with home-based sessions over 12 weeks. They will be led by an Huntsman Cancer Institute (HCI) fitness specialist and will consist of light stretching exercises; while avoiding a focus on meditation.

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
55 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Significant fatigue as assessed during screening with the NCI Common Terminology Criteria for Adverse Events (CTCAE) Safety Profiler of fatigue using a cut-off value of ≥ 1; and/or with a fatigue grading scale (general questions that assess level of fatigue currently and in the past week from a scale of 0-100) with a cut off value of \>20 * Are sedentary as defined by \<150 minutes of mild, moderate, or intense intensity exercise/week per Centers for Disease Control and Prevention(CDC) guidelines * Able to speak and read English fluently, and understand informed consent * Reside within 60 miles of Huntsman Cancer Institute and have access to regular transportation to all assessments and intervention classes at HCI * Willing to: sign a medical record release form; be randomized and willing to participate in classes and all baseline and follow-up appointments * Significant others and domestic partners of elderly prostate cancer survivors will be eligible if they are at least 18 years of age, read and speak English, willing to sign an informed consent, and provide a physician's release for exercise

Exclusion criteria

* Clinical evidence of metastatic disease other than elevated prostate-antigen specific (PSA) levels * Current practice of Qigong, Tai Chi or other similar types of Complementary and Alternative medicine that may share similar principles of Qigong * Inability to pass the Folstein Mini Mental Status Exam (score \<23) * Unable to drive or secure transportation to complete all aspects of the study * Health conditions (e.g. severe hearing loss, respiratory, cardiovascular, or neurological problems) that might interfere with the required intervention * Unwilling to be randomized to study groups and/or commit to 12 weeks of Qigong or non-aerobic stretching classes

Design outcomes

Primary

MeasureTime frameDescription
Retention Rate in Study (Feasibility Outcome)13-weeksThe retention rate was the proportion of participants who remained enrolled in the study and completed post-intervention measures. Range of retention rate is 0 to 1. Prostate cancer survivors were the population targeted in this intervention, therefore, the retention and attendance rates only include prostate cancer survivors (i.e., family members were not included in these calculations).
Attendance Rates in Study (Feasibility Outcome)13-weeksThe class attendance rates were the number of classes attended by participants divided by the total number of classes offered. Range of attendance rate is 0 to 1. Prostate cancer survivors were the population targeted in this intervention, therefore, the retention and attendance rates only include prostate cancer survivors (i.e., family members were not included in these calculations).
FACIT-Fatigue Change From Baseline to 13-weeks.Baseline to 13-weeksOur primary outcome of change in fatigue was assessed with the Functional Assessment Chronic Illness Therapy (FACIT)-Fatigue scale. This 13-item scale assesses levels of fatigue during daily activities over the past seven days. Higher scores indicate less fatigue (score range = 0 - 52). Positive change scores indicate improved fatigue.

Secondary

MeasureTime frameDescription
Brief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksBaseline to 13-weeksThe BSI-18 assesses global distress and three subscales (anxiety, depression, & somatization). Scores are converted to T-scores based on US population norms. Negative change scores indicate improvement in distress. We report data separately for prostate cancer survivors and family members. Based on the population norm a T-score of 63 or above indicates heightened global distress.

Countries

United States

Participant flow

Recruitment details

We recruited 502 senior prostate cancer survivors in Utah through clinic referrals, registries, community advertisements, and community-based support groups.

Pre-assignment details

Out of 89 prostate cancer survivors screened for eligibility, forty were eligible and interested in participating in the study.Twenty family members met criteria for participating. Only the survivors were randomized to study arms. Family members attended the study arm that the survivor was randomized to.

Participants by arm

ArmCount
Qigong
Qigong originated in China hundreds of years ago and has been practiced for centuries. It consists of a sequence of slow, flowing physical movements with concentration on the breath and awareness and may promote physical and mental relaxation and energy balance. Qigong : Classes will be 60 minutes in duration, held two times a week, supplemented with home-based sessions over 12 weeks. The classes will be led by a trained Qigong instructor and consist of postures, movements, deep breathing techniques and meditation. It will include eccentrically-biased Qigong movements with an emphasis on weight shifting and posture control. The continuous body movements coupled with progressively diminishing base of support, dynamic challenge to balance, and concentration on body positions requiring eccentric muscle activity should improve the levels of fatigue and quality of life in older prostate cancer survivors.
30
Stretching Control
The non-aerobic stretching will serve as an attention control group to control for non-specific factors; dose of attention and to mimic being in a group setting. Non-aerobic stretching : The non-aerobic stretching classes will serve as an attention control. They will be 60 minutes in duration, held two times a week, supplemented with home-based sessions over 12 weeks. They will be led by an Huntsman Cancer Institute (HCI) fitness specialist and will consist of light stretching exercises; while avoiding a focus on meditation.
30
Total60

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject610

Baseline characteristics

CharacteristicStretching ControlQigongTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
21 Participants23 Participants44 Participants
Age, Categorical
Between 18 and 65 years
9 Participants7 Participants16 Participants
Age, Continuous71.2 years
STANDARD_DEVIATION 10.1
71.3 years
STANDARD_DEVIATION 9.6
71.2 years
STANDARD_DEVIATION 9.7
Region of Enrollment
United States
30 participants30 participants60 participants
Sex: Female, Male
Female
9 Participants10 Participants19 Participants
Sex: Female, Male
Male
21 Participants20 Participants41 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 300 / 30
serious
Total, serious adverse events
0 / 300 / 30

Outcome results

Primary

Attendance Rates in Study (Feasibility Outcome)

The class attendance rates were the number of classes attended by participants divided by the total number of classes offered. Range of attendance rate is 0 to 1. Prostate cancer survivors were the population targeted in this intervention, therefore, the retention and attendance rates only include prostate cancer survivors (i.e., family members were not included in these calculations).

Time frame: 13-weeks

ArmMeasureValue (NUMBER)
QigongAttendance Rates in Study (Feasibility Outcome)0.85 Proportion of classes
Stretching ControlAttendance Rates in Study (Feasibility Outcome)0.68 Proportion of classes
Primary

FACIT-Fatigue Change From Baseline to 13-weeks.

Our primary outcome of change in fatigue was assessed with the Functional Assessment Chronic Illness Therapy (FACIT)-Fatigue scale. This 13-item scale assesses levels of fatigue during daily activities over the past seven days. Higher scores indicate less fatigue (score range = 0 - 52). Positive change scores indicate improved fatigue.

Time frame: Baseline to 13-weeks

Population: Data is presented for Qigong participants (n=16) and family members (n=8 ) and for Stretching participants (n=13) and family members (n=7) .

ArmMeasureGroupValue (MEDIAN)
QigongFACIT-Fatigue Change From Baseline to 13-weeks.Prostate Cancer Survivor FACIT-Fatigue Change5.0 Units on scale
QigongFACIT-Fatigue Change From Baseline to 13-weeks.Family Member FACIT-Fatigue Change2.5 Units on scale
Stretching ControlFACIT-Fatigue Change From Baseline to 13-weeks.Prostate Cancer Survivor FACIT-Fatigue Change0.0 Units on scale
Stretching ControlFACIT-Fatigue Change From Baseline to 13-weeks.Family Member FACIT-Fatigue Change0.0 Units on scale
Primary

Retention Rate in Study (Feasibility Outcome)

The retention rate was the proportion of participants who remained enrolled in the study and completed post-intervention measures. Range of retention rate is 0 to 1. Prostate cancer survivors were the population targeted in this intervention, therefore, the retention and attendance rates only include prostate cancer survivors (i.e., family members were not included in these calculations).

Time frame: 13-weeks

ArmMeasureValue (NUMBER)
QigongRetention Rate in Study (Feasibility Outcome)0.80 proportion of participants
Stretching ControlRetention Rate in Study (Feasibility Outcome)0.65 proportion of participants
Secondary

Brief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeks

The BSI-18 assesses global distress and three subscales (anxiety, depression, & somatization). Scores are converted to T-scores based on US population norms. Negative change scores indicate improvement in distress. We report data separately for prostate cancer survivors and family members. Based on the population norm a T-score of 63 or above indicates heightened global distress.

Time frame: Baseline to 13-weeks

Population: Data is presented for Qigong participants (n=16) and family members (n=8 ) and for Stretching participants (n=13) and family members (n=7) .

ArmMeasureGroupValue (MEDIAN)
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Global Index Change-7.0 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Anxiety Change-7.5 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Somatization Change-6.5 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Depression Change-6.5 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Global Index Change-3.5 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Anxiety Change-1.0 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Somatization Change0.0 T-Score
QigongBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Depression Change-5.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Depression Change-3.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Global Index Change0.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Global Index Change-2.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Anxiety Change0.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Somatization Change0.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Somatization Change0.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksFamily Member Anxiety Change-7.0 T-Score
Stretching ControlBrief Symptom Inventory (BSI)-18 Change From Baseline to 13-weeksProstate Cancer Survivors Depression Change0.0 T-Score

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026