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Purpose

The researchers hope to learn if yoga complementary therapy would improve health-related quality of life, recovery of urinary continence and erectile function in patients who underwent prostate cancer surgery (i.e. radical prostatectomy). We hypothesized that in patients undergoing radical prostatectomy, preoperative and postoperative Yoga complementary therapy would improve health- related quality of life (HRQOL), recovery of urinary continence and erectile function. This two-arm, randomized controlled pilot study will compare Yoga intervention to usual care group. The aim is to evaluate the efficacy of Yoga complementary therapy on HRQOL in patients who underwent radical prostatectomy (RP). Yoga therapy will be given to the intervention group three times in a week for 6 weeks prior to surgery and then initiated 3 weeks after the surgery for another 6 weeks. The yoga exercise will be tailored to the participant's comfort level. As an exploratory analysis, we will evaluate pro-inflammatory and immunological markers.

Condition

Eligibility

Eligible Ages
Between 30 Years and 80 Years
Eligible Genders
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Men between the age of 30 to 80 - Has been diagnosed with localized prostate cancer (i.e. pathologically and/or radiographically confirmed) - Is scheduled to undergo radical prostatectomy (i.e. robot-assisted or open-approach) - Has no other active primary malignancy aside from prostate cancer - Currently not practicing yoga as a form of exercise and/or meditation - Does not have uncontrolled pain - Does not have neurological or musculoskeletal co-morbidity inhibiting exercise - Has never been diagnosed by health care professionals to have absolute contraindications to exercise testing - Willing to be randomized to either standard care or intervention group - Willing to participate in yoga therapy for twelve weeks if randomized to intervention group - Willing to undergo phlebotomy - Able and willing to provide informed consent

Exclusion Criteria

  • Men under the age of 30 or over the age of 80 - Has NOT been diagnosed with localized prostate cancer (i.e. pathologically and/or radiographically confirmed) - Is NOT scheduled to undergo radical prostatectomy (i.e. robot-assisted or open-approach) - Has other active primary malignancy aside from prostate cancer - Currently practicing yoga as a form of exercise and/or meditation - Has uncontrolled pain - Has neurological or musculoskeletal co-morbidity inhibiting exercise - Has been diagnosed with psychotic, addictive, and major cognitive disorders - Has been diagnosed by health care professionals to have absolute contraindications to exercise testing Unwilling to be randomized to either standard care or intervention group - Unwilling to participate in yoga therapy for twelve weeks if randomized to intervention group - Unwilling to undergo phlebotomy - Unable and unwilling to provide informed consent

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Supportive Care
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
No Intervention
Standard Care 		Those assigned to the standard care group will follow the routine pre- and post-operative care for patients whose undergoing radical prostatectomy.
Active Comparator
Yoga therapy group 		Those assigned to the yoga therapy group will be asked to participate in yoga session three times in a week for 6 weeks prior to the scheduled surgery and then re-initiated 3 weeks after the surgery for another 6 weeks. Each session will be approximately 60 - 75 minutes. These yoga session will be held at Nydia's Yoga Therapy Studio, located in San Antonio, TX, under the guidance of certified yoga instructor, Dr. Nydia Tijerina Darby, PT, DPT, MS, who's the owner of the studio and co-investigator of this study. The yoga exercise will be tailored to patient's comfort level.
  • Behavioral: Yoga therapy

More Details

Status
Completed
Sponsor
The University of Texas Health Science Center at San Antonio

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.