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Effects of Physical Exercise on Postmenopausal Risk Factors in Women With Osteopenia (ACTLIFE)

Primary Purpose

Osteopenia, Osteoporosis

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
High Intensity Resistance (HIT-RT) and Endurance exercise (HIIT)
Wellness
Sponsored by
University of Erlangen-Nürnberg Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteopenia, Osteoporosis

Eligibility Criteria

48 Years - 58 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • (early)postmenopausal women, ( normal menopause, 1-5 years post)
  • Osteopenia and osteoporosis at the lumbar spine or femoral neck Bone Mineral Density (BMD) <-1.0 standard deviation (SD) T-Score, WHO)

Exclusion Criteria:

  • BMD <-4.0 SD T-Score (BMD threshold for pharmaceutical therapy according to Dachverband Osteologie (DVO) guideline (mandatory for Germany, Austria, Suisse) for woman 50-60 years).
  • Prevalent clinical, low-trauma fractures
  • Diseases and drugs with relevant effects on bone and muscle metabolism (e.g. glucocorticoids >7.5 mg/d or bisphosphonate therapy); individual case assessment
  • Diseases and drugs with relevant effects on cardiometabolic risk factors (e.g. severe hypertension with corresponding medical therapy); individual case assessment
  • Severe cardiovascular events (e.g. stroke, coronary infarction) in the past.
  • Other conditions, diseases that exclude exercise training in a group (≤10 persons).

Sites / Locations

  • Institute of Medical Physics, Friedrich Alexander University Erlangen-Nürnberg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

exercise

control

Arm Description

Exercise group

active control group

Outcomes

Primary Outcome Measures

BMD Lumbar Spine
Bone Mineral Density (BMD) at the lumbar spine region of interest as determined by Dual Energy x-Ray Absorptiometry (DXA)

Secondary Outcome Measures

BMD total Hip
Bone Mineral Density at the total hip region of interest as determined by DXA
Para-vertebral muscle density
Muscle density at the para-vertebral region as determined by Magnetic Resonance Imaging (MRI)
Mid-thigh muscle density
Muscle density at the mid-thigh region as determined by MRI
Metabolic Syndrome
Metabolic Syndrome Z-Score according to the Internationale Diabetes Federation (IDF)
Visceral body fat
Visceral body fat as determined by Magnetic Resonance Imaging (MRI)
Total body fat
Total body fat as determined by whole body DXA
Total Lean Body Mass
Total Lean Body Mass as determined by whole body DXA
Menopausal complaints
Menopausal complaints as determined by the Menopause Rating Scale (German version. Questionnaire with 11 items; scale from 0 (no complaints/problems) to 4 (very severe complaints/problem)
Maximum leg strength
Maximum isokinetic leg extensor strength as determined by an isokinetic leg press
Total fat rate
Total fat rate as determined by Bio Impedance technique (BIA)
Fat free mass
Fat free mass as determined by BIA

Full Information

First Posted
May 20, 2019
Last Updated
June 5, 2020
Sponsor
University of Erlangen-Nürnberg Medical School
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1. Study Identification

Unique Protocol Identification Number
NCT03959995
Brief Title
Effects of Physical Exercise on Postmenopausal Risk Factors in Women With Osteopenia
Acronym
ACTLIFE
Official Title
Effects of an Optimized 13-month Physical Exercise on (Early)-Postmenopausal Risk Factors in Women With Osteopenia and Osteoporosis (Actlife)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
January 15, 2019 (Actual)
Primary Completion Date
March 13, 2020 (Actual)
Study Completion Date
June 5, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Erlangen-Nürnberg Medical School

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Menopause usually have a serious impact on a woman's life, associated with negative consequences for health and quality of life. Early preventive assessments are very difficult to implement due to the complex hormone-deficiency-induced effects on a large variety of organs and systems with estrogen receptors. In fact, only a few types of interventions have the potential to comprehensively improve the various risk factors and complaints of the menopausal transition. In detail, however, not every form of exercise training or every training protocol is effective for exerting positive effects on selected risk factors. In particular, the training concept for addressing musculoskeletal or cardio-metabolic risk factors differ fundamentally. In several studies, we confirmed the effect of different complex training programs on risk factors of different postmenopausal female cohorts with special consideration of osteoporotic aspects. The training programs applied in this context were characterized by the consistent implementation of recognized training principles and an in general exercise intensity-oriented approach. Recent studies confirmed the effectiveness of this proceeding for women with relevant postmenopausal risk factors including low bone strength. However, the crucial issue of the most effective, feasible and easily customizable training protocol for addressing postmenopausal risk factors remains to be answered, taking into account that the majority of exercise programs were realized in an ambulatory group setting. The aim of the study will be to evaluate the effects of an optimized physical training on risk factors and complaints of (early) postmenopausal women with special consideration of the osseous fracture risk. Note (05.06.2020): Of importance, the intervention has to be cancelled due to COVID-19 lockdown in March 2020 after 13 months of intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteopenia, Osteoporosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
Blinding attempt of participants by sham exercise. Outcome assessors were unaware of participant's group status (exercise or control) and were not allowed to ask correspondingly.
Allocation
Randomized
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
exercise
Arm Type
Experimental
Arm Description
Exercise group
Arm Title
control
Arm Type
Sham Comparator
Arm Description
active control group
Intervention Type
Other
Intervention Name(s)
High Intensity Resistance (HIT-RT) and Endurance exercise (HIIT)
Intervention Description
Ambulatory, consistently supervised group exercise training (3 training sessions of 40-45 min/week each). 10-12-week blocks of non-linearly periodized high intensity resistance and high impact aerobic dance exercises (HIT-setting) intermitted by 4-6-week periods of endurance-type exercise with high volume and lower intensity. Indi-vidualized training schedules for the RT-section.
Intervention Type
Other
Intervention Name(s)
Wellness
Intervention Description
control group: 3x 10 week blocks, 1 training session/week à 45 min; stretching, light functional gymnastics, yoga with less strengthening techniques over 13 months.
Primary Outcome Measure Information:
Title
BMD Lumbar Spine
Description
Bone Mineral Density (BMD) at the lumbar spine region of interest as determined by Dual Energy x-Ray Absorptiometry (DXA)
Time Frame
from baseline to 13 month follow-up
Secondary Outcome Measure Information:
Title
BMD total Hip
Description
Bone Mineral Density at the total hip region of interest as determined by DXA
Time Frame
from baseline to 13 month follow-up
Title
Para-vertebral muscle density
Description
Muscle density at the para-vertebral region as determined by Magnetic Resonance Imaging (MRI)
Time Frame
from baseline to 13 month follow-up
Title
Mid-thigh muscle density
Description
Muscle density at the mid-thigh region as determined by MRI
Time Frame
from baseline to 13 month follow-up
Title
Metabolic Syndrome
Description
Metabolic Syndrome Z-Score according to the Internationale Diabetes Federation (IDF)
Time Frame
from baseline to 13 month follow-up
Title
Visceral body fat
Description
Visceral body fat as determined by Magnetic Resonance Imaging (MRI)
Time Frame
from baseline to 13 month follow-up
Title
Total body fat
Description
Total body fat as determined by whole body DXA
Time Frame
from baseline to 13 month follow-up
Title
Total Lean Body Mass
Description
Total Lean Body Mass as determined by whole body DXA
Time Frame
from baseline to 13 month follow-up
Title
Menopausal complaints
Description
Menopausal complaints as determined by the Menopause Rating Scale (German version. Questionnaire with 11 items; scale from 0 (no complaints/problems) to 4 (very severe complaints/problem)
Time Frame
from baseline to 13 month follow-up
Title
Maximum leg strength
Description
Maximum isokinetic leg extensor strength as determined by an isokinetic leg press
Time Frame
from baseline to 13 month follow-up
Title
Total fat rate
Description
Total fat rate as determined by Bio Impedance technique (BIA)
Time Frame
from baseline to 13 month follow-up
Title
Fat free mass
Description
Fat free mass as determined by BIA
Time Frame
from baseline to 13 month follow-up

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
early postmenopausal
Minimum Age & Unit of Time
48 Years
Maximum Age & Unit of Time
58 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (early)postmenopausal women, ( normal menopause, 1-5 years post) Osteopenia and osteoporosis at the lumbar spine or femoral neck Bone Mineral Density (BMD) <-1.0 standard deviation (SD) T-Score, WHO) Exclusion Criteria: BMD <-4.0 SD T-Score (BMD threshold for pharmaceutical therapy according to Dachverband Osteologie (DVO) guideline (mandatory for Germany, Austria, Suisse) for woman 50-60 years). Prevalent clinical, low-trauma fractures Diseases and drugs with relevant effects on bone and muscle metabolism (e.g. glucocorticoids >7.5 mg/d or bisphosphonate therapy); individual case assessment Diseases and drugs with relevant effects on cardiometabolic risk factors (e.g. severe hypertension with corresponding medical therapy); individual case assessment Severe cardiovascular events (e.g. stroke, coronary infarction) in the past. Other conditions, diseases that exclude exercise training in a group (≤10 persons).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Hettchen, MSc
Organizational Affiliation
Institute of Medical Physics, University of Erlangen-Nürnberg, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Medical Physics, Friedrich Alexander University Erlangen-Nürnberg
City
Erlangen
State/Province
Bavaria
ZIP/Postal Code
91052
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Physical Exercise on Postmenopausal Risk Factors in Women With Osteopenia

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