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Effect of PROGRESSive Training and Teststerone in Older Frail Men (PROGRESS)

Primary Purpose

Muscle Weakness

Status
Unknown status
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
testosterone
Progressive muscle training
Sponsored by
University Hospital, Gentofte, Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Muscle Weakness focused on measuring older, frail, men, progressive muscle training, muscle training, exercise, testosterone

Eligibility Criteria

70 Years - undefined (Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

Living in their own home or in sheltered accommodation. Independent gait possible. with tool. Capable of stand-up and sit in a chair at least 8 times in 30 sec. There must be at least 3 symptoms or objective findings of low testosterone . Serum testosterone <10nmol /L as the average of two independent measurements

-

Exclusion Criteria:

Known or previous prostate cancer. Abnormally elevated serum PSA (PSA = prostate specific antigen) corresponding to PSA> 5 ng / ml or PSA> 0.15 ng / ml / cc (relative to the prostatic volume in cubic centimeters (cc)). Hæmatomacrose. Heart disease in the form of: peri-, myo-, or endocarditis, angina, severe heart failure (NYHA class III and IV), severe hypertension (systolic blood pressure> 180 or diastolic BT> 105 mmHg after antihypertensive therapy). Dyspnoea at rest. Liver (AST> 2 x ULN) or renal impairment (serum creatinine> 200 micromoles / L). Severe and insufficiently treated epilepsy or migraine. Insulin treatment. Previous or current bifosfonat-, fluoride, HRT, SERM-, strontium, teraparatid- or more than 3 weeks of prednisolone. Joint disease with acute inflammation. Active cancer disease in chemo- or radiotherapy. Bone metabolic disease apart from age-related osteoporosis. Autoimmune diseases, chronic systemic diseases (cirrhosis, AIDS, chronic renal failure). Primary testosterone deficiency in the form of testicular dysgenesis, Klinefelter syndrome (47, XXY), 46, XX males, LH-resistance, the Y chromosome deletions, other sex chromosome abnormalities ,. Significant abuse, mental illness, dementia, physical disability with inability to implement intervention or tests or to give informed consent. Contraindications to testosterone undecanoate is included in the exclusion criteria, such as. presence of liver tumors, breast and prostate cancer, as subjects will be examined before the trial starts.

Sites / Locations

  • Karsten OvergaardRecruiting
  • Medical Dept. O, Geriatric SectionRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

No Intervention

Experimental

Experimental

Experimental

Arm Label

Controls

Testosterone

Training

Testosterone and training

Arm Description

A control group, which is 20 weeks with placebo injections without training.

A testosterone group given 20 weeks on testosterone injections without training

A Training Group, which is 20 weeks with placebo injections and 16 weeks of progressive resistance training supplemented with vitamin D and protein supplements

A combination group that is 20 weeks with testosterone injections and 16 weeks of progressive resistance training supplemented with vitamin D and protein supplements

Outcomes

Primary Outcome Measures

Stand-up-and Sit-test
It is a measure of overall strength in the lower extremities. Result of the test is defined as the number of times the participant can stand up and sit from a chair in 30 seconds. There is a good correlation (r = 0.78) with a leg press and an acceptable test-retest reliability (ICC = 0.86).

Secondary Outcome Measures

Frequency and severity of falls via questionaire
included in the monitoring of adverse events.
Balance ability,
Tandem Test containing three starting positions: 1) Standing with feet together, standing in the semi-tandem position and standing in the tandem stand. coupled with decrease risk of fall.
Avlund mobility scale
Questions about experiencing fatigue and support needs of ordinary everyday activities. Avlund mobility scale is correlated with the isometric muscle strength, simple function tests , increased risk of hospitalization and mortality
Leg extensor Power Rig test
An instrument for measuring muscle strength in the lower extremities.
Isometric muscle strength
Measurement of isometric muscle strength m. quadriceps in a seated leg press.
Armflexion Test:
Measures of overall strength in the upper extremities. The number of times the participant can inflect the elbow with dumbbell is measured in 30 sec.
2-minute knee lift test:
Measures aerobic capacity in the elderly. Number of high knee lifts in 2 minutes.
2,45minute up-and-go test:
Target for basic mobility in the elderly. Time it takes to rise from a chair, walk around a cone 2,45m away, go back and sit down again. Moderate to good correlation between the corresponding 3m test and Berg Balance Scale (r = 0.81), walking speed (r = 0.61) and Barthel index (r = 0.78) and a good test-retest- reliability (ICC = 0.98).
DXA scan
Lean body mass. Measurement of fat and fat-free mass and total bone mass (BMC). Executed only at baseline and at study end.
Bone Mineral Density
Of the spine, distal forearm bilaterally, total hip bilaterally and in the skeleton as a whole (total body). In case of osteoporosis treatment will be initiated following the department's usual guidelines, which can blur the results for bone density.
Major Depression Inventory (MDI):
Questionnaire on depression and mental well-being.
Montreal Cognitive Assessment (MoCA):
A cognitive screening test that provides an estimate of the intellectual functioning; This test is also sensitive to mild cognitive problems and dementia.
Quality of Life EQ-5D:
Questionnaire on the experienced quality of life.
Modified PISQ-12:
An assessment of sexual performance (potency) and sexual desire. There are previously found improved sexual function, mood, muscle strength and body composiAn evaluation questionnaire of sexual function
Aastrands Test:
Sub-maximal fitness test performed on a treadmill. Includes monitoring heart rate
Measurements of the Heart Rate Variability (HRV)
Studies have indicated that hypogonodal men can improve the Heart Rate Variability by testosterone treatment
Dual-energy X-ray absorptiometry
Measurement of the body composition bioimpedance.
Safety parameters - blood pressure
Blood pressure. Blood samples: Serum testosterone, hemoglobin, hematocrit, lipid profile, Potassium, Natrium, creatinine, CRP, AST, bilirubin, alkaline phosphatase, TSH, p-ionized calcium, PTH, Ca ++, and 25-OH vitamin D.
Side effects
Measuring a lot of posssible side effects to training and testosterone
Safety parameters - blood sample - testosterone level
Measuring levels of testosterone and safely parameter
Safety parameters - blood sample - hemoglobin level
Measuring levels hemoglobin
Safety parameters - blood sample - hematocrit level
Measuring levels of hematocrit
Safety parameters - blood sample - lipid profile
Measuring levels cholesterol
Safety parameters - blood sample - Potassium
Measuring levels of potassium
Safety parameters - blood sample - Natrium
Measuring levels of natrium
Safety parameters - blood sample - creatinine
Measuring levels of creatinine
Safety parameters - blood sample - CRP
Measuring levels of CRP
Safety parameters - blood sample - Aspartate aminotransferase (AST)
Measuring levels of aspartate aminotransferase (AST)
Safety parameters - blood sample - bilirubin
Measuring levels of bilirubin
Safety parameters - blood sample - alkaline phosphatase
Measuring levels of alkaline phosphatase
Safety parameters - blood sample - Thyreoid Stimulating Hormone (TSH)
Measuring levels of TSH
Safety parameters - blood sample - p-ionized calcium
Measuring levels of p-ionized calcium
Safety parameters - blood sample - PTH
Measuring levels of PTH
Safety parameters - blood sample - Ca ++
Measuring levels of Ca2+
Safety parameters - blood sample - 25-OH vitamin D.
Measuring levels of vitamin D

Full Information

First Posted
August 12, 2016
Last Updated
March 25, 2021
Sponsor
University Hospital, Gentofte, Copenhagen
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1. Study Identification

Unique Protocol Identification Number
NCT02873559
Brief Title
Effect of PROGRESSive Training and Teststerone in Older Frail Men
Acronym
PROGRESS
Official Title
Effect of PROGRESSive Resistance Training, Protein Supplements and Testosterone in Older Frail Men With Testosterone Deficiency (PROGRESS Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2016 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
January 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Gentofte, Copenhagen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In this scientific clinical investigation we will test whether testosterone and progressive resistance training can improve muscle strength and reduce the risk of falls in older men. In addition, we will examine whether this treatment improves quality of life, functional capacity, including sexual function and counteracts depression. Such a project have not been performed earlier.
Detailed Description
Project background: In Denmark more than 1,000 people each year die of a fall, which is more than five times as many dying in traffic accidents. Fall accidents are also the leading cause of traumatic brain injury and is a relatively unnoticed problem, although this type of accidents causes more hospital bed days than all other accidents combined. Annually, almost half of the 375,000 elderly Danes over 75 years of age and relatively three times as many of the approximately 40,000 elderly people in nursing homes fall every year, causing over 40,000 hospital contacts annually. Ten percent of all elderly people hospitalized each year because of a fall, mostly with fractures, for which the risk increases fivefold after a fall. In Denmark there are now now around 1 million people over 65 years of age. Over the next 25 years we will experience a 50% growth to 1.5 million people over 65 years of age. Injury, disability and death caused by falls is therefore a widespread and growing human and societal problem. Many will never recover completely and will therefore need help to cope with everyday life. After the first fall risk increase for repeated falls. Especially for older people living in their own homes permanent or temporary disabilities results in a severe deterioration of the quality of life. Treatment of falls is also a significant financial burden on health and social care. The main reason for the decline is muscle weakness. Muscle weakness leads to greatly increased risk of falling, decreased quality of life and functional capacity. Musclemass and -power decrease about 40 percent from age 20 to 80 years old. Recent studies have shown that even 90-year-old persons can double their muscle strength by intensive training just three times per week. The level of the male sex hormone testosterone decreases with age and leads to impaired muscle mass. Twenty percent of men over 60 and 50 percent over 80 years, a low level of testosterone in total equivalent to more than 100,000 Danes. From the human and socio-economic perspective, it is important to find treatments that can enhance function in the elderly.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Weakness
Keywords
older, frail, men, progressive muscle training, muscle training, exercise, testosterone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
196 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Controls
Arm Type
No Intervention
Arm Description
A control group, which is 20 weeks with placebo injections without training.
Arm Title
Testosterone
Arm Type
Experimental
Arm Description
A testosterone group given 20 weeks on testosterone injections without training
Arm Title
Training
Arm Type
Experimental
Arm Description
A Training Group, which is 20 weeks with placebo injections and 16 weeks of progressive resistance training supplemented with vitamin D and protein supplements
Arm Title
Testosterone and training
Arm Type
Experimental
Arm Description
A combination group that is 20 weeks with testosterone injections and 16 weeks of progressive resistance training supplemented with vitamin D and protein supplements
Intervention Type
Drug
Intervention Name(s)
testosterone
Intervention Description
Testosterone supplemented in 5 months
Intervention Type
Other
Intervention Name(s)
Progressive muscle training
Other Intervention Name(s)
Training
Intervention Description
Progressive muscle training during 4 months
Primary Outcome Measure Information:
Title
Stand-up-and Sit-test
Description
It is a measure of overall strength in the lower extremities. Result of the test is defined as the number of times the participant can stand up and sit from a chair in 30 seconds. There is a good correlation (r = 0.78) with a leg press and an acceptable test-retest reliability (ICC = 0.86).
Time Frame
up to 5 months (at study completion)
Secondary Outcome Measure Information:
Title
Frequency and severity of falls via questionaire
Description
included in the monitoring of adverse events.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Balance ability,
Description
Tandem Test containing three starting positions: 1) Standing with feet together, standing in the semi-tandem position and standing in the tandem stand. coupled with decrease risk of fall.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Avlund mobility scale
Description
Questions about experiencing fatigue and support needs of ordinary everyday activities. Avlund mobility scale is correlated with the isometric muscle strength, simple function tests , increased risk of hospitalization and mortality
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Leg extensor Power Rig test
Description
An instrument for measuring muscle strength in the lower extremities.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Isometric muscle strength
Description
Measurement of isometric muscle strength m. quadriceps in a seated leg press.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Armflexion Test:
Description
Measures of overall strength in the upper extremities. The number of times the participant can inflect the elbow with dumbbell is measured in 30 sec.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
2-minute knee lift test:
Description
Measures aerobic capacity in the elderly. Number of high knee lifts in 2 minutes.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
2,45minute up-and-go test:
Description
Target for basic mobility in the elderly. Time it takes to rise from a chair, walk around a cone 2,45m away, go back and sit down again. Moderate to good correlation between the corresponding 3m test and Berg Balance Scale (r = 0.81), walking speed (r = 0.61) and Barthel index (r = 0.78) and a good test-retest- reliability (ICC = 0.98).
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
DXA scan
Description
Lean body mass. Measurement of fat and fat-free mass and total bone mass (BMC). Executed only at baseline and at study end.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Bone Mineral Density
Description
Of the spine, distal forearm bilaterally, total hip bilaterally and in the skeleton as a whole (total body). In case of osteoporosis treatment will be initiated following the department's usual guidelines, which can blur the results for bone density.
Time Frame
At baseline, 1 month, 5 months (at study completion
Title
Major Depression Inventory (MDI):
Description
Questionnaire on depression and mental well-being.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Montreal Cognitive Assessment (MoCA):
Description
A cognitive screening test that provides an estimate of the intellectual functioning; This test is also sensitive to mild cognitive problems and dementia.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Quality of Life EQ-5D:
Description
Questionnaire on the experienced quality of life.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Modified PISQ-12:
Description
An assessment of sexual performance (potency) and sexual desire. There are previously found improved sexual function, mood, muscle strength and body composiAn evaluation questionnaire of sexual function
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Aastrands Test:
Description
Sub-maximal fitness test performed on a treadmill. Includes monitoring heart rate
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Measurements of the Heart Rate Variability (HRV)
Description
Studies have indicated that hypogonodal men can improve the Heart Rate Variability by testosterone treatment
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Dual-energy X-ray absorptiometry
Description
Measurement of the body composition bioimpedance.
Time Frame
At baseline, 1 month, 5 months (at study completion)
Title
Safety parameters - blood pressure
Description
Blood pressure. Blood samples: Serum testosterone, hemoglobin, hematocrit, lipid profile, Potassium, Natrium, creatinine, CRP, AST, bilirubin, alkaline phosphatase, TSH, p-ionized calcium, PTH, Ca ++, and 25-OH vitamin D.
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Side effects
Description
Measuring a lot of posssible side effects to training and testosterone
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - testosterone level
Description
Measuring levels of testosterone and safely parameter
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - hemoglobin level
Description
Measuring levels hemoglobin
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - hematocrit level
Description
Measuring levels of hematocrit
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - lipid profile
Description
Measuring levels cholesterol
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - Potassium
Description
Measuring levels of potassium
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - Natrium
Description
Measuring levels of natrium
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - creatinine
Description
Measuring levels of creatinine
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - CRP
Description
Measuring levels of CRP
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - Aspartate aminotransferase (AST)
Description
Measuring levels of aspartate aminotransferase (AST)
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - bilirubin
Description
Measuring levels of bilirubin
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - alkaline phosphatase
Description
Measuring levels of alkaline phosphatase
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - Thyreoid Stimulating Hormone (TSH)
Description
Measuring levels of TSH
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - p-ionized calcium
Description
Measuring levels of p-ionized calcium
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - PTH
Description
Measuring levels of PTH
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - Ca ++
Description
Measuring levels of Ca2+
Time Frame
Measured every four weeks through the study (for 5 months)
Title
Safety parameters - blood sample - 25-OH vitamin D.
Description
Measuring levels of vitamin D
Time Frame
Measured every four weeks through the study (for 5 months)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Living in their own home or in sheltered accommodation. Independent gait possible. with tool. Capable of stand-up and sit in a chair at least 8 times in 30 sec. There must be at least 3 symptoms or objective findings of low testosterone . Serum testosterone <10nmol /L as the average of two independent measurements - Exclusion Criteria: Known or previous prostate cancer. Abnormally elevated serum PSA (PSA = prostate specific antigen) corresponding to PSA> 5 ng / ml or PSA> 0.15 ng / ml / cc (relative to the prostatic volume in cubic centimeters (cc)). Hæmatomacrose. Heart disease in the form of: peri-, myo-, or endocarditis, angina, severe heart failure (NYHA class III and IV), severe hypertension (systolic blood pressure> 180 or diastolic BT> 105 mmHg after antihypertensive therapy). Dyspnoea at rest. Liver (AST> 2 x ULN) or renal impairment (serum creatinine> 200 micromoles / L). Severe and insufficiently treated epilepsy or migraine. Insulin treatment. Previous or current bifosfonat-, fluoride, HRT, SERM-, strontium, teraparatid- or more than 3 weeks of prednisolone. Joint disease with acute inflammation. Active cancer disease in chemo- or radiotherapy. Bone metabolic disease apart from age-related osteoporosis. Autoimmune diseases, chronic systemic diseases (cirrhosis, AIDS, chronic renal failure). Primary testosterone deficiency in the form of testicular dysgenesis, Klinefelter syndrome (47, XXY), 46, XX males, LH-resistance, the Y chromosome deletions, other sex chromosome abnormalities ,. Significant abuse, mental illness, dementia, physical disability with inability to implement intervention or tests or to give informed consent. Contraindications to testosterone undecanoate is included in the exclusion criteria, such as. presence of liver tumors, breast and prostate cancer, as subjects will be examined before the trial starts.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Karsten Overgaard, M.D.
Phone
+45 2617 2611
Email
karstenovergaard20@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rune S. Rasmussen, MA, PhD
Phone
+45 2875 7500
Email
rsr@sund.ku.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karsten Overgaard, M.D.
Organizational Affiliation
Herlev Hospital, Neurological Department N108
Official's Role
Study Director
Facility Information:
Facility Name
Karsten Overgaard
City
Hellerup
State/Province
Danmark
ZIP/Postal Code
DK-2900
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karsten Overgaard, neurologist
Phone
+45 2617 2611
Email
karstenovergaard20@hotmail.com
First Name & Middle Initial & Last Name & Degree
Rune Rasmussen, PhD neuropsy
Phone
+45 2875 7500
Email
rsr@sund.ku.dk
First Name & Middle Initial & Last Name & Degree
Mette Midttun, M.D. DMSci
Facility Name
Medical Dept. O, Geriatric Section
City
Herlev
ZIP/Postal Code
2730
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mette Midttun, MD, DMSc
Phone
+45 38689188
Email
mette.midttun@regionh.dk
First Name & Middle Initial & Last Name & Degree
Mette Midttun, MD, DMSc

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29500160
Citation
Rasmussen R, Midttun M, Kolenda T, Ragle AM, Sorensen TW, Vinther A, Zerahn B, Pedersen M, Overgaard K. Therapist-Assisted Progressive Resistance Training, Protein Supplements, and Testosterone Injections in Frail Older Men with Testosterone Deficiency: Protocol for a Randomized Placebo-Controlled Trial. JMIR Res Protoc. 2018 Mar 2;7(3):e71. doi: 10.2196/resprot.8854.
Results Reference
derived
Links:
URL
https://www.researchprotocols.org/2018/3/e71
Description
Therapist-Assisted Progressive Resistance Training, Protein Supplements, and Testosterone Injections in Frail Older Men with Testosterone Deficiency: Protocol for a Randomized Placebo-Controlled Trial
URL
http://www.jgerontology-geriatrics.com/article/view/285
Description
Testosterone serum levels in elderly fall-prone men do not correlate with age or performance in the 30 seconds chair stand test

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Effect of PROGRESSive Training and Teststerone in Older Frail Men

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