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Efficacy of physical exercise on muscle mass and strength in prostate cancer patients receiving androgen deprivation therapy

Efficacy of physical exercise on muscle mass and strength in prostate cancer patients receiving androgen deprivation therapy: A prospective study - Efficacy of physical exercise in prostate cancer patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057982
Enrollment
120
Registered
2025-06-01
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Prostate cancer patients receiving hormonal therapy (androgen deprivation therapy)

Interventions

All participants are asked to perform physical exercise in their daily lives. Physical excercise is performed as a home program. A home program includes excercises recommended by the Ministry of Heal
1.Walking of 8000 steps a day, three times per week, 2.Diary locomotor-training. All subjects were asked to keep a diary about how well they were able to perform these exercises. Based on a diary and
patients who performed a lot of exercise therapy (80% or more), ones who performed it to a certain extent (40-80%), and the group who performed it very little (less than 40%). All data are compared in

Sponsors

Kanazawa University Graduate School of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. The patients with locally advanced prostate cancer receiving hormonal therapy and radical radiotherapy, or the patients with painless metastatic prostate cancer receiving hormonal therapy. 2. The patients with a written informed consent to attend the present study. 3. The patients aged over 20 years.

Exclusion criteria

Exclusion criteria: 1. The prostate cancer therapy patients with metastatic prostate cancer and with a risk of bone fracture (bone scan index of more than 3.0% based on bone scan). 2. The patients with cardiovascular diseases, locomotor diseases, or neurologic disorders, which are not suitable for exercise therapy. 3. The patients who are deemed inappropriate by an attending doctor.

Design outcomes

Primary

MeasureTime frame
Changes in systemic muscle mass, Lower limb muscle mass, and grip power (items associated with sarcopenia) 3, 6, 9. 12, 18, 24, 30, and 36 months after initiation of ADT.

Secondary

MeasureTime frame
The following items before and after the start of treatment: 1. Height, weight, BMI, body fat percentage, and waist circumference 2. Locomotor syndrome test 3. Short Physical Performance Battery 4. Clinical Frailty Scale 5. Bone mineral content (evaluated at the femoral neck) 6. Skeletal muscle index at L3 level on CT (L3-SMI)

Countries

Japan

Contacts

Public ContactKazuyoshi Shigehara

Kanazawa University Graduate School of Medical Science Department of Integrative Cancer Therapy and Urology

kshigehara0415@yahoo.co.jp076-265-2393

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026