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CompletedNCT04144127Updated Aug 22, 2023Results posted

Soccer Intervention in Prostate Cancer Survivors

An interventional study of Soccer in Prostate Cancer, sponsored by Emory University. Completed at 1 site in United States. Open to male participants aged 18 Years to 79 Years. Per ClinicalTrials.gov, last updated 2023-08-22.

Sponsored by Emory University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
3
Allocation
Not applicable
Ages
18 Years to 79 Years
Sex
Male
01

Study summary

This study seeks to directly test the implementation feasibility of a soccer-based and lifestyle education intervention to determine the effects on bone health, body composition, mental health, functional and cardiometabolic status among prostate cancer survivors.

Read the detailed description

Prostate cancer (PCa) is the most common cancer in men in the U.S. and in other industrialized countries. The lifetime probability of PCa in males is one in nine, and it has a high economic burden, with costs expected to rise. Modern tailored treatment approaches, including androgen deprivation therapy (ADT), have resulted in longer life expectancy, but also longer treatment periods, which lead to significant adverse side effects. These often include decreased bone mineral density (BMD), increased risk of fractures, low functional capacity, loss of lean body mass (LBM), increased fat mass, insulin resistance, psychological distress and pain. Of particular concern is a sharp decline in bone health, with systemic bone loss caused by PCa-produced osteoclastogenic cytokines and drug interventions. Independent of disease stage, fractures in PCa patients are predictors of survival. In addition, concomitant physical inactivity and stress during and after treatment predispose PCa patients to elevated risk of deconditioning, BMD loss, cardiovascular and metabolic disease morbidity and mortality.

Exercise-based lifestyle interventions aimed at counteracting treatment-induced adverse effects have been shown to be safe and effective in improving bone, functional and cardiometabolic health for patients with PCa. However, men, in general, are harder to engage in physical activity (PA) and lifestyle interventions. As an alternative to traditional exercise programs, recreational team sports provide a unique environment that may lead to increased physical activity participation and motivation to engage in other lifestyle changes. More than any other sport, recreational soccer (RS) has been shown to be a successful health intervention in patients with, or at risk of chronic diseases, including PCa.

Leveraging the growing enthusiasm around soccer in Atlanta and the U.S. may lead to increased interest, participation, retention and engagement in lifestyle change programming among PCa survivors. Therefore, this study seeks to directly test the implementation feasibility of a soccer-based lifestyle change intervention to determine the effect on bone health, body composition, mental health, functional and cardiometabolic status among PCa survivors.

Participants will be offered an intensive intervention including RS programming and lifestyle education. The group will receive RS, consisting of conditioning drills and games, adapted to the population during 60-minute sessions twice per week. The researchers will evaluate health outcomes at baseline and after 3 months of the intervention.

02

Conditions studied

  • Prostate Cancer

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03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's enrollment of 3 is below the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Emory University is the lead sponsor of 1,386 studies on the registry; 236 are open to participants now.

Of its 229 completed or terminated interventional studies of FDA-regulated products, 174 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 79 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  1. men aged 18-79 years
  2. PCa survivors that had at least 6 months of hormone therapy (i.e. ADT with testosterone lowering agents) within the past 10 years
  3. not engaged in soccer practice or other exercise or lifestyle intervention program for the past 12 months
  4. availability of smartphone to receive text messages
  5. treating Oncologist clearance
  6. ability to read in English or Spanish and provide informed consent

Exclusion criteria

Exclusion Criteria:

  1. BMI > 40 kg/m\^2
  2. resting BP ≥170/100 at screening or uncontrolled hypertension
  3. any mobility issues or exercise program contraindications
  4. a recent (i.e., within 12 months) myocardial infarction, diagnosis of congestive heart disease, other active cancer
  5. bone or organ metastases
  6. chemotherapy within past 6 months
  7. therapies and diseases of bone unrelated to PCa e.g. systemic glucocorticoids, bisphosphonates, teriparatide, denosumab, osteomalacia; osteosarcoma; Paget's disease; systemic lupus erythematosus; inflammatory bowel diseases, rheumatoid arthritis; thyroid/parathyroid disorder or mental illness
  8. not coronavirus disease 2019 (COVID-19) vaccinated
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
3 participants (actual)

Study arms

  • Experimental
    Soccer Group

    Participants in the soccer group will participate in soccer drills and other fitness routines (two 1-hour sessions per week). They will meet with the soccer coach after the soccer sessions to discuss the lifestyle education topics (Life's Simple 7 education topics). During the soccer sessions participants will be fitted with a wearable soccer-specific device to measure how much they move and their heart rate. All participants will receive a Garmin Vivofit wearable device to help monitor their PA goals and achievements.

    Behavioral: Soccer

Interventions

  • BehavioralSoccer

    * Soccer drills and other fitness routines (two 1-hour sessions per week) * In person education in Life's Simple 7 to help improve life through Lifestyle changes: smoking status, physical activity, weight, diet, blood glucose, cholesterol, and blood pressure.

    Also known as: Recreational Soccer (RS)

06

What researchers measure

Primary outcomes

  1. Lumbar Spine Bone Mineral Density (BMD)

    Bone mineral density will be measured by dual x-ray absorptiometry (DXA) scan at the lumbar spine (L2-L4). Decreased BMD a is associated with an increased risk of fractures.

    Time frame: Baseline, 3 months post-intervention

Secondary outcomes

  1. Total Hip BMD

    Bone mineral density will be measured by dual x-ray absorptiometry (DXA) scan at the hip. Decreased BMD a is associated with an increased risk of fractures.

    Time frame: Baseline, 3 months post-intervention

  2. Osteocalcin Level

    Osteocalcin is marker of bone formation. The normal range for osteocalcin varies by lab and elevated levels are seen in patients with bone diseases characterized by increased bone turnover.

    Time frame: Baseline, 3 months post-intervention

  3. C-terminal Telopeptide of Collagen (CTx)

    C-terminal telopeptide of collagen (CTx) is a bone resorption marker. Increased levels indicate increased bone resorption with conditions such as osteoporosis and osteopenia.

    Time frame: Baseline, 3 months post-intervention

  4. Weight

    Weight is measured in kilograms (kg).

    Time frame: Baseline, 3 months post-intervention

  5. Body Mass Index (BMI)

    Body Mass Index (BMI) is weight in kilograms divided by the square of height in meters.

    Time frame: Baseline, 3 months post-intervention

  6. Percentage of Body Fat

    Body fat is measured by dual x-ray absorptiometry (DXA) scan.

    Time frame: Baseline, 3 months post-intervention

  7. Waist Circumference

    Waist circumference is measured in centimeters (cm).

    Time frame: Baseline, 3 months post-intervention

  8. Lean Body Mass

    Lean body mass is body weight minus weight from body fat.

    Time frame: Baseline, 3 months post-intervention

  9. Resting Heart Rate

    The normal resting heart rate in adults is between 60 and 100 beats per minute (bpm). A lower resting heart rate indicates that the person has better fitness as the heart is working more efficiently.

    Time frame: Baseline, 3 months post-intervention

  10. Systolic Blood Pressure

    Systolic blood pressure (BP) will be measured while sitting using a calibrated electronic blood pressure sphygmomanometer at Baseline and at 3 months post-intervention. A normal systolic blood pressure reading is lower than 120 mmHg. BP values higher than 120 mmHg correlate with worse outcome.

    Time frame: Baseline, 3 months post-intervention

  11. Diastolic Blood Pressure

    Diastolic blood pressure (BP) will be measured while sitting using a calibrated electronic blood pressure sphygmomanometer prior to any activity (Baseline) and at 3 months post-intervention. A normal diastolic blood pressure reading is lower than 80 mmHg. BP values higher than 80 mmHg correlate with worse outcome.

    Time frame: Baseline, 3 months post-intervention

  12. Aerobic Capacity

    Aerobic capacity is measured by 6 minute walk test distance (meters).

    Time frame: Baseline, 3 months post-intervention

  13. Muscle Strength

    Muscle strength is measured as hand grip strength (kg). Hand grip was measured using a study approved dynamometer to test the maximum isometric strength of the hand and forearm muscles of the dominant hand. An increase in values means that grip strength is improving.

    Time frame: Baseline, 3 months post-intervention

  14. Behavioral Regulation in Exercise Questionnaire-2 (BREQ-2) Score

    Physical activity self-efficacy is assessed with the BREQ-2 instrument. The BREQ-2 has 19 items measuring motivation to exercise, with 5 motivational styles examined: intrinsic regulation (the respondent finds physical activity enjoyable), identified regulation (the respondent sees benefits of physical activity), introjected regulation (physical activity is done to increase self-esteem or avoid negative feelings with not performing exercise), external regulation (physical activity is done based on rewards or punishments from someone else), and amotivation (the respondent has no motivation to engage in physical activity). Responses are given on a 5 point Likert scale where 0=not true for me, and 4=very true for me. A relative autonomy index (RAI) can be calculated by weighting the scores for each motivational style factor. The weights range from 3 to -3 and total RAI scores range from -24 to 20. Higher scores indicate greater self-determined motivation to engage in physical activity.

    Time frame: Baseline, 3 months post-intervention

  15. Dietary Intake

    The dietary intake is measured using the Nutrition Database System for Research (NDSR) 24-hour dietary recall. The NDSR is a dietary analysis software application used to collect and calculate nutritional intake.

    Time frame: Baseline, 3 months post-intervention

  16. Number of Participants Smoking Cigarettes

    Smoking habits are assessed with the National Health and Nutrition Examination Survey (NHANES) 2019-2020 for smoking and tobacco use. This instrument includes 24 items and the number of questions that a respondent answers depends on their past and current smoking behaviors. Participants are asked if they currently smoke cigarettes and possible responses are: "every day", "some days", and "not at all".

    Time frame: Baseline, 3 months post-intervention

  17. Alcohol Habits

    Number of alcohol beverages per week will be recorded.

    Time frame: Baseline, 3 months post-intervention

  18. Sleep Time

    Average sleep time will be collected in minutes per day.

    Time frame: Baseline, 3 months post-intervention

  19. Weekly Steps

    Participants will be asked to wear a Garmin fitness tracker throughout the study and physical activity will be measured as steps taken per week.

    Time frame: Baseline, 3 months post-intervention

  20. SF-12 Health Survey Score

    Quality of life is assessed with the SF-12 Health Survey. The SF-12 is a multipurpose, standardized self-report short form survey with 12 questions assessing mental and physical functioning. The SF-12 consists of 12 items with a Likert-type response format that measures quality of life with a Physical Component Summary (PCS) and Mental Component Summary (MCS). Subscales associated with the PCS include physical functioning, role limitations due to physical problems, bodily pain, and general health perceptions. Subscales associated with the MCS include vitality (energy and fatigue), social functioning, role limitations due to emotional problems, and mental health. A scoring algorithm is used to generate a total score for each component ranging from 0 to 100. Low values represent a poor health state while high values represent a good health state.

    Time frame: Baseline, 3 months post-intervention

  21. Center for Epidemiologic Studies Depression Scale (CESD) Score

    Symptoms of depression are assessed with the CESD. The CESD is a 20-item questionnaire asking about feelings and behaviors during the past week. Responses are given on a 4-point scale where 0 = rarely or none of the time (less than 1 day), 1 = some or a little of the time (1-2 days), 2 = occasionally or a moderate amount of time (3-4 days), and 3 = most or all of the time (5-7 days). Scores range from 0 to 60 with high scores indicating greater depressive symptoms.

    Time frame: Baseline, 3 months post-intervention

07

Results

Posted Aug 22, 2023

Participant flow

Participant flow — Overall Study
MilestoneSoccer Group
Started3
Completed3
Not completed0

Outcome measures

PrimaryLumbar Spine Bone Mineral Density (BMD)

Bone mineral density will be measured by dual x-ray absorptiometry (DXA) scan at the lumbar spine (L2-L4). Decreased BMD a is associated with an increased risk of fractures.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · mg/cm^3
Lumbar Spine Bone Mineral Density (BMD)
mg/cm^3Soccer Group
Baseline1.2 ± 0.3
3 months post-intervention1.2 ± 0.3
SecondaryTotal Hip BMD

Bone mineral density will be measured by dual x-ray absorptiometry (DXA) scan at the hip. Decreased BMD a is associated with an increased risk of fractures.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · mg/cm^3
Total Hip BMD
mg/cm^3Soccer Group
Baseline1.2 ± 0.1
3 months post-intervention1.2 ± 0.1
SecondaryOsteocalcin Level

Osteocalcin is marker of bone formation. The normal range for osteocalcin varies by lab and elevated levels are seen in patients with bone diseases characterized by increased bone turnover.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondaryC-terminal Telopeptide of Collagen (CTx)

C-terminal telopeptide of collagen (CTx) is a bone resorption marker. Increased levels indicate increased bone resorption with conditions such as osteoporosis and osteopenia.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondaryWeight

Weight is measured in kilograms (kg).

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · Kg
Weight
KgSoccer Group
Baseline111.6 ± 10.4
3 months post-intervention106.6 ± 11.1
SecondaryBody Mass Index (BMI)

Body Mass Index (BMI) is weight in kilograms divided by the square of height in meters.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · kg/m^2
Body Mass Index (BMI)
kg/m^2Soccer Group
Baseline34.1 ± 1.7
3 months post-intervention32.7 ± 2.0
SecondaryPercentage of Body Fat

Body fat is measured by dual x-ray absorptiometry (DXA) scan.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · % of body fat
Percentage of Body Fat
% of body fatSoccer Group
Baseline42.1 ± 3.3
3 months post-intervention40.9 ± 2.9
SecondaryWaist Circumference

Waist circumference is measured in centimeters (cm).

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · cms
Waist Circumference
cmsSoccer Group
Baseline120.6 ± 0.5
3 months post-intervention117.3 ± 0.5
SecondaryLean Body Mass

Lean body mass is body weight minus weight from body fat.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · lbs
Lean Body Mass
lbsSoccer Group
Baseline138.9 ± 16.9
3 months post-intervention135.7 ± 17.9
SecondaryResting Heart Rate

The normal resting heart rate in adults is between 60 and 100 beats per minute (bpm). A lower resting heart rate indicates that the person has better fitness as the heart is working more efficiently.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondarySystolic Blood Pressure

Systolic blood pressure (BP) will be measured while sitting using a calibrated electronic blood pressure sphygmomanometer at Baseline and at 3 months post-intervention. A normal systolic blood pressure reading is lower than 120 mmHg. BP values higher than 120 mmHg correlate with worse outcome.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · mmHg
Systolic Blood Pressure
mmHgSoccer Group
Baseline140.3 ± 15.9
3 months post-intervention126.3 ± 22.3
SecondaryDiastolic Blood Pressure

Diastolic blood pressure (BP) will be measured while sitting using a calibrated electronic blood pressure sphygmomanometer prior to any activity (Baseline) and at 3 months post-intervention. A normal diastolic blood pressure reading is lower than 80 mmHg. BP values higher than 80 mmHg correlate with worse outcome.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · mmHg
Diastolic Blood Pressure
mmHgSoccer Group
Baseline79 ± 12.5
3 months post-intervention68.3 ± 11.9
SecondaryAerobic Capacity

Aerobic capacity is measured by 6 minute walk test distance (meters).

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · meters
Aerobic Capacity
metersSoccer Group
Baseline536.7 ± 80.8
3 months post-intervention497.7 ± 54.1
SecondaryMuscle Strength

Muscle strength is measured as hand grip strength (kg). Hand grip was measured using a study approved dynamometer to test the maximum isometric strength of the hand and forearm muscles of the dominant hand. An increase in values means that grip strength is improving.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · Kg
Muscle Strength
KgSoccer Group
Baseline36.1 ± 4.3
3 months post-intervention37.7 ± 4.4
SecondaryBehavioral Regulation in Exercise Questionnaire-2 (BREQ-2) Score

Physical activity self-efficacy is assessed with the BREQ-2 instrument. The BREQ-2 has 19 items measuring motivation to exercise, with 5 motivational styles examined: intrinsic regulation (the respondent finds physical activity enjoyable), identified regulation (the respondent sees benefits of physical activity), introjected regulation (physical activity is done to increase self-esteem or avoid negative feelings with not performing exercise), external regulation (physical activity is done based on rewards or punishments from someone else), and amotivation (the respondent has no motivation to engage in physical activity). Responses are given on a 5 point Likert scale where 0=not true for me, and 4=very true for me. A relative autonomy index (RAI) can be calculated by weighting the scores for each motivational style factor. The weights range from 3 to -3 and total RAI scores range from -24 to 20. Higher scores indicate greater self-determined motivation to engage in physical activity.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondaryDietary Intake

The dietary intake is measured using the Nutrition Database System for Research (NDSR) 24-hour dietary recall. The NDSR is a dietary analysis software application used to collect and calculate nutritional intake.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondaryNumber of Participants Smoking Cigarettes

Smoking habits are assessed with the National Health and Nutrition Examination Survey (NHANES) 2019-2020 for smoking and tobacco use. This instrument includes 24 items and the number of questions that a respondent answers depends on their past and current smoking behaviors. Participants are asked if they currently smoke cigarettes and possible responses are: "every day", "some days", and "not at all".

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondaryAlcohol Habits

Number of alcohol beverages per week will be recorded.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondarySleep Time

Average sleep time will be collected in minutes per day.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondaryWeekly Steps

Participants will be asked to wear a Garmin fitness tracker throughout the study and physical activity will be measured as steps taken per week.

Time frame:
Baseline, 3 months post-intervention

No measurements were reported for this outcome.

SecondarySF-12 Health Survey Score

Quality of life is assessed with the SF-12 Health Survey. The SF-12 is a multipurpose, standardized self-report short form survey with 12 questions assessing mental and physical functioning. The SF-12 consists of 12 items with a Likert-type response format that measures quality of life with a Physical Component Summary (PCS) and Mental Component Summary (MCS). Subscales associated with the PCS include physical functioning, role limitations due to physical problems, bodily pain, and general health perceptions. Subscales associated with the MCS include vitality (energy and fatigue), social functioning, role limitations due to emotional problems, and mental health. A scoring algorithm is used to generate a total score for each component ranging from 0 to 100. Low values represent a poor health state while high values represent a good health state.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · score on a scale
SF-12 Health Survey Score
score on a scaleSoccer Group
Baseline PCS44.2 ± 17.4
3 months post-intervention PCS47.2 ± 9.5
Baseline MCS53.2 ± 8.7
3 months post-intervention MCS53.6 ± 4.9
SecondaryCenter for Epidemiologic Studies Depression Scale (CESD) Score

Symptoms of depression are assessed with the CESD. The CESD is a 20-item questionnaire asking about feelings and behaviors during the past week. Responses are given on a 4-point scale where 0 = rarely or none of the time (less than 1 day), 1 = some or a little of the time (1-2 days), 2 = occasionally or a moderate amount of time (3-4 days), and 3 = most or all of the time (5-7 days). Scores range from 0 to 60 with high scores indicating greater depressive symptoms.

Time frame:
Baseline, 3 months post-intervention
Reported as:
Mean · score on a scale
Center for Epidemiologic Studies Depression Scale (CESD) Score
score on a scaleSoccer Group
Baseline4.3 ± 5.9
3 months post-intervention5.3 ± 5.9

Adverse events

Collected over Up to 3 months post-intervention.. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Soccer Group0/3 (0%)0/3 (0%)0/3 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Soccer Group
<=18 years0
Between 18 and 65 years0
>=65 years3
Sex: Female, Male
Sex: Female, Male(Participants)Soccer Group
Female0
Male3
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Soccer Group
Hispanic or Latino0
Not Hispanic or Latino3
Unknown or Not Reported0
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Soccer Group
American Indian or Alaska Native0
Asian0
Native Hawaiian or Other Pacific Islander0
Black or African American0
White3
More than one race0
Unknown or Not Reported0
Region of Enrollment
Region of Enrollment(participants)Soccer Group
United States3
08

Study locations

1 site
  • Emory University Hospital
    Atlanta, Georgia 30322, United States
09

References and documents

Study documents

  • Protocol and statistical analysis plan · Sep 7, 2021
  • Informed consent form · Sep 7, 2021

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT04144127
Lead sponsor
Emory University
Collaborators
National Cancer Institute (NCI)
Responsible party
Roberto Felipe Lobelo (Associate Professor, Emory University) — Principal investigator
First posted
Oct 30, 2019
Start date
Oct 25, 2019
Primary completion
Jul 15, 2022
Completion
Jul 15, 2022
Results posted
Aug 22, 2023
Last update
Aug 22, 2023

Study contacts

Roberto Felipe Lobelo, MD
principal investigator · Emory University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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