Virginia Commonwealth University
Richmond, Virginia, 23298, United States
NCT Number: NCT06250751
To refine a remote behavioral exercise training intervention for testing in a larger randomized trial.
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Notify Me41 year–85 year
Male
Interventional
Not applicable
Richmond, Virginia, 23298, United States
Determine feasibility of recruiting a sample of medically underserved prostate cancer patients undergoing treatment with Androgen Deprivation Therapy (ADT) to a remotely delivered (i.e., home-based) exercise intervention and determine the interventions acceptability.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
To be eligible men, transwomen or non-binary individuals must meet the following criteria:
Introduce and refine concept of exercise and cardiovascular health by initiating walking or cycling and provide behavioral counseling sessions to foster support for adoption and maintenance of exercise, and to troubleshoot barriers. During the first two weeks, the study team will meet with participants twice per week (virtually) to introduce the intervention, familiarize men with the exercise program, exercise logs, resistance bands for strength training. Contact will drop to once per week during weeks 3-8 (total=10 contacts in weeks 1-8). Behavioral counseling will be delivered by the PI or the study coordinator for 30-40 minutes prior to 20-30 mins of an individual or group-based strength training class.
Time frame: Day 1
The number of participants that enroll
Time frame: 12 Weeks
The number of participants that complete greater than 80% of the planned assessments
Time frame: 12 Weeks
Number of participants that adhere to and complete the intervention
Time frame: Baseline, 8 Weeks, and 12 Weeks
An ActivPAL is a small, previously validated thigh-worn device that continuously measures physical activity, sitting time or movement. An Actigraph is a small wrist worn device that continuously measures physical activity intensity (i.e., exercise intensity), sleep time or movement.
Time frame: Baseline, 8 Weeks, and 12 Weeks
The average of the scores for participants using the GLTEQ is a 3-item measure used to classify participant's activity levels per week. The Weekly leisure activity score = (9 × Strenuous) + (5 × Moderate) + (3 × Light). The Godin scale score = 24 units or more=active, 14-23 units= moderately active, and less than 14 unites = insufficiently active/ sedentary.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Measuring changes in a 6 minute walk distance. The participant has a goal to walk as fast, but safely, as possible without running for a period of 6 minutes.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Short Physical Performance Battery (Short Physical Performance Battery (SPPB) is a battery of 3 tests (standing balance, gait speed and char stands) that are combined to assess overall physical function. Each test is scored on a scale of 1-4 with 4 being reflective of good function and 0 of poor function. Overall scores of 10 or less are reflective of mobility limitations.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Participants will be first asked to stand from a sitting position without using their arms. If they can perform the task, they will then be asked to stand up and sit down as many times as possible in a 30 second period. The greater the number of chair stands the better the lower body strength.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Grip strength will be assessed using an isometric handgrip dynamometer while the participant is seated with the head facing straight ahead. The elbow should be bent at a 90-degree angle and the wrist should be at the mid-prone position. The participant should exert maximally and quickly (about 1 second) and two trials should be made alternately with each hand, with at least 30 seconds between trials for the same hand (recorded in kilograms).
Time frame: Baseline, 8 Weeks, and 12 Weeks
The Exercise Self-Efficacy Scale assesses an individual's beliefs in their ability to continue exercising on a three time per week basis at moderate intensities for 40+ minutes per session in the future. For each item, participants indicate their confidence to execute the behavior on a 100-point percentage scale comprised of 10-point increments, ranging from 0% (not at all confident) to 100% (highly confident). Total strength for each measure of self-efficacy is then calculated by summing the confidence ratings and dividing by the total number of items in the scale, resulting in a maximum possible efficacy score of 100.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Assessment of the level of support individuals making health-behavior changes (exercise) felt they were receiving from family and friends.
Family Participation: sum items 11 - 16 and 20 - 23 Family Rewards and Punishment (an optional scale): sum items 17 - 19 Friend Participation: sum items 11 - 16 and 20 - 23
Higher scores reflect more support.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Walk Score measures the walkability of any address using a patented system. For each address, Walk Score analyzes hundreds of walking routes to nearby amenities. Points are awarded based on the distance to amenities in each category. Amenities within a 5 minute walk (.25 miles) are given maximum points.
90-100 is a good walk score 70-89 is very walkable 50-69 is somewhat walkable 0-49 is car dependent
Time frame: Baseline, 8 Weeks, and 12 Weeks
The FACIT-fatigue scale is a 13-item scale that has been widely used in many studies to assess cancer related fatigue
Scores range from 0-52 with higher scores indicating better quality of life.
Time frame: Baseline, 8 Weeks, and 12 Weeks
The FACT-P measure is composed of the FACT-General which assesses four primary HRQOL domains: physical well-being , functional well-being, social well-being, and emotional well-being and an additional component for prostate specific concerns.
Scores range from 0-156 with higher scores reflecting better quality of life
Time frame: Baseline, 8 Weeks, and 12 Weeks
The SF-36 is perhaps the most widely used measure of health status and includes domains of vitality and physical function.
The SF-36 has 8 subdomains (physical functioning, role limitations due to physical health, role limitations due to emotional problems, energy/fatigue, emotional well-being, social functioning, pain, general health). Each scale item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively with 100 higher quality of life.
Time frame: Baseline, 8 Weeks, and 12 Weeks
PROMIS - Fatigue is a validated self-report measure of fatigue among patients diagnosed with cancer and higher scores indicate a lower level of fatigue. All scores are on a T-score distribution with a mean of 50 and standard deviation of 10.
Time frame: Baseline, 8 Weeks, and 12 Weeks
PROMIS - Physical function is a validated self-report measure of physical function among patients diagnosed with cancer and higher scores indicate better functioning. All scores are on a T-score distribution with a mean of 50 and standard deviation of 10.
Time frame: Baseline, 8 Weeks, and 12 Weeks
PROMIS - Anxiety is a validated self-report measure of physical function among patients diagnosed with cancer and higher scores indicate better functioning. All scores are on a T-score distribution with a mean of 50 and standard deviation of 10.
Time frame: Baseline, 8 Weeks, and 12 Weeks
PROMIS - Depression is a validated self-report measure of physical function among patients diagnosed with cancer and higher scores indicate better functioning. All scores are on a T-score distribution with a mean of 50 and standard deviation of 10.
Time frame: Baseline, 8 Weeks, and 12 Weeks
PROMIS - Sleep disturbance is a validated self-report measure of physical function among patients diagnosed with cancer and higher scores indicate better functioning. All scores are on a T-score distribution with a mean of 50 and standard deviation of 10.
Time frame: Baseline, 8 Weeks, and 12 Weeks
Social Determinants of Health (SDOH) questionnaire is a self-administered questionnaire used to examine education and income variables in relation to cardiovascular risk. The questionnaire is administered at the baseline visit. We will also ask about difficult paying for basics and experience of racial discrimination at 3- and 6-month follow up visits.
Virginia Commonwealth University
Other
Behavioral Exercise TRaining for Medically Underserved Men Undergoing Androgen Deprivation Therapy for Prostate Cancer (BETR-PC)
Acronym: BETR-PC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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