Efficacy and Safety of the Physical Activity Program in Women With Post-menopausal Osteoporosis (ACTLIFE)
Primary Purpose
Osteoporosis, Postmenopausal, Physical Activity
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Physical activity
Sponsored by
About this trial
This is an interventional other trial for Osteoporosis, Postmenopausal focused on measuring osteoporosis, Gym Training, physical activity, home training
Eligibility Criteria
Inclusion Criteria:
- signed informed consent
- post menopausal women aged >40 years (with or without history of fractures, with or without pharmacological therapy for OP)
- lumbar spine or femur T-score ≤-2,5
- functional motor capacity normal or moderately reduced (Short Physical Performance Battery)
- sedentary life style (having exercised less than 30 minutes per week in the last 6 months).
Exclusion Criteria are:
- secondary OP49, impairment of communicative and/or sensorial functions so severe to make impossible understanding or executing trainer's instructions (dementia, aphasia, blindness, deafness);
- heart failure (NYHA class >2);
- unstable angina, pulmonary disease requiring oxygen therapy;
- symptomatic peripheral arteriopathy;
- myocardial infarction or hospital admission in the previous 6 months,
- symptomatic orthostatic hypotension;
- hypertension in poor pharmacologic control (diastolic >95 mmHg, systolic >160 mmHg),
- previous implant of prosthesis at upper or lower limbs,
- relevant neurological condition impairing motor or cognitive function, any other condition that the medical doctor (MD) considers to contraindicate the participation in an exercise program of moderate intensity.
Sites / Locations
- Istituto Ortopedico Rizzoli
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Gym Trainer
Individual Home
Arm Description
Physical Activity program is performed in a group in a gym (Gym Group Training-GGT), with activity sessions conducted by a trainer graduated in Science and Techniques of Preventive and Adapted Physical Activity
Physical Activity program is performed at home individually (Individual Home Training-IHT), without the supervision of a trainer during the exercise session.
Outcomes
Primary Outcome Measures
Quality of life questionnaire
Assessment of health related quality of life in osteoporosis - ECOS-16 questionnaire measures the HRQoL in postmenopausal women with osteoporosis. The 16 items are divided into 4 dimensions.
The score of each item ranges from 1 to 5. A single summary score obtained from the arithmetic mean of the answered items, so the total score ranges from 1 (best HRQoL) to 5 (worst HRQoL).
Secondary Outcome Measures
Disability
WHODAS has six domains of life
Cognition understanding and communicating
Mobility
Self-care
Getting along
Life activities Summing of recorded item scores within each domain after the converting the summary score into a metric raging from 0 to 100 ( 0 = no disability - 100 = full disability)
Fear of falls
Falls Efficacy Scale International - FES-I The score contains 16 items scored on a four point scale (1= not all concerned to 4= very concerned
To calculate the FES-I or Short FES-I score when all items are completed, simply add the scores for each item together to give a total that ranges as follows:
Minimum 16 (no concern about falling) to maximum 64 (severe concern about falling)
Walking
6-Minute Walk Test The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance (m) covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.
An increase in the distance walked indicates improvement in basic mobility.
standing balance
Standing balance will be estimated by the validated Stability Index for both right and left lower limb.
It evaluates proprioceptive control, visual dependence, and the risk of fall and injury.
The Stability Index is a score (0-100 %). 100% is high
Muscle force
Hand grip (KG)
joint mobility
Hip range of motion in degree, knee range of motion in degree, shoulder range of motion in degree
Body Mass Index
Weight and height will be combined to report BMI in kg/m^2
Full Information
NCT ID
NCT04179903
First Posted
June 4, 2019
Last Updated
September 22, 2023
Sponsor
Istituto Ortopedico Rizzoli
Collaborators
University of Bologna
1. Study Identification
Unique Protocol Identification Number
NCT04179903
Brief Title
Efficacy and Safety of the Physical Activity Program in Women With Post-menopausal Osteoporosis
Acronym
ACTLIFE
Official Title
Efficacy and Safety of the Exercise Program in Women With Post-menopausal Osteoporosis: Randomized Trial Comparing Gym Versus Home Training
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
September 30, 2020 (Actual)
Study Completion Date
June 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Ortopedico Rizzoli
Collaborators
University of Bologna
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study will be single blinded since professionals who will evaluate patients will not know to which exercise group patients have been assigned.
The investigators hypothesize that effectiveness and safety of the exercise program are equal when administered as gym trainer or individual home trainer. However, the investigators expect differences in adherence among the two groups which may cause different impact on the outcome measures.
Given the large amount of evidence on the efficacy of Physical Activity in women with Osteoporosis, the investigators considered it ethically unacceptable to advise a control group inactivity. On the other hand, it seemed particularly relevant for the purpose of addressing the advice to the improvement of the active lifestyle, to evaluate the impact of the ACTLIFE exercise program when administered as gym trainer or individual home trainer
Detailed Description
The present study is carried out within the project "Physical ACTivity: the tool to improve the quality of LIFE in osteoporosis people" (ACTLIFE) and is funded within the Erasmus Plus Sport program (Grant Agreement N2017-2128/001-001).
It is aimed at evaluating differences in efficacy and safety of a PA program specifically designed for improving physical function and, here in after, QoL in post menopausal women with Osteoporosis (T-score <-2,5) under usual pharmacological treatment, when administered as gyms as group training (GGT) or Individual Home Training IHT. During the study patients will be recommended to maintain their usual pharmacological treatment for OP, as prescribed.
The primary objective of the study is to compare modifications of QoL measured with the Short Osteoporosis Quality of Life Questionnaire (ECOS-16) induced by the ACTLIFE exercise programme when administered as IHT or GGT. ECOS-16 is a specific-disease instrument with the purpose to measure the health related QoL (HRQoL) in post menopausal women with OP.
The secondary objectives of the study are to investigate differences between IHT and GGT on domains which are considered to be determinants of QoL:
WHO Disability Assessment Schedule (WHODAS) which evaluates the six activity and participation domains of the International Classification of Functioning, Disability and Health (ICF): cognition, mobility, self-care, interacting with other people, life activities, participation.
Fear of falls evaluated by the Falls Efficacy Scale International (FES-I);
Walking (6-Minute Walk Test), standing balance (stability Index), muscle force (hand grip), postural alignment (occiput-wall distance) and joint mobility will be also evaluated as fundamental prerequisites of motor behavior;
Body Mass index and body composition.
The adherence of each patient to the exercise program will be monitored. The adherence will be measured as percent of exercise sessions actually performed /total number of scheduled exercise sessions. The investigators hypothesize that effectiveness and safety of the exercise program are equal when administered as GGT or IHT. However, the investigators expect differences in adherence among the two groups which may cause different impact on the outcome measures. In the context of the evaluation of adherence to the program, the satisfaction of the participants for the ACTLIFE program administered as GGT or IHT at the end of the 12 months of exercise will be evaluated with a specific questionnaire based on 7-point Likert scale and the reasons of abandoning the exercise program (question with structured answers). Education attainment, work activity, marital status and home-gym distance will be also recorded since recognized to influence the adherence in an exercise program.
The ultimate goal of the ACTLIFE exercise program is to increase physical activity in a sedentary population. The exercise program, through its beneficial effects on health, is expected to generate a virtuous circle of greater activity and participation. In this context, to evaluate differences between GGT or IHT, the investigators introduced in the study protocol the Physical Activity Scale for the Elderly (PASE). PASE is an easily scored survey designed specifically to measure the weekly physical activity in adult and aged population. Its score combines information on leisure, household and occupational activity.
RT with two parallel groups: in the first group the 12-month ACTLIFE program is performed as IHT, while in the second as GGT. The study will be single blinded since professionals who will evaluate patients will not know to which exercise group they have been assigned. Patients will be assessed at baseline and after 6 and 12 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis, Postmenopausal, Physical Activity
Keywords
osteoporosis, Gym Training, physical activity, home training
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
52 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Gym Trainer
Arm Type
Active Comparator
Arm Description
Physical Activity program is performed in a group in a gym (Gym Group Training-GGT), with activity sessions conducted by a trainer graduated in Science and Techniques of Preventive and Adapted Physical Activity
Arm Title
Individual Home
Arm Type
Active Comparator
Arm Description
Physical Activity program is performed at home individually (Individual Home Training-IHT), without the supervision of a trainer during the exercise session.
Intervention Type
Other
Intervention Name(s)
Physical activity
Intervention Description
Physical Activity program is performed in a group in a gym and at home
Primary Outcome Measure Information:
Title
Quality of life questionnaire
Description
Assessment of health related quality of life in osteoporosis - ECOS-16 questionnaire measures the HRQoL in postmenopausal women with osteoporosis. The 16 items are divided into 4 dimensions.
The score of each item ranges from 1 to 5. A single summary score obtained from the arithmetic mean of the answered items, so the total score ranges from 1 (best HRQoL) to 5 (worst HRQoL).
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Disability
Description
WHODAS has six domains of life
Cognition understanding and communicating
Mobility
Self-care
Getting along
Life activities Summing of recorded item scores within each domain after the converting the summary score into a metric raging from 0 to 100 ( 0 = no disability - 100 = full disability)
Time Frame
12 months
Title
Fear of falls
Description
Falls Efficacy Scale International - FES-I The score contains 16 items scored on a four point scale (1= not all concerned to 4= very concerned
To calculate the FES-I or Short FES-I score when all items are completed, simply add the scores for each item together to give a total that ranges as follows:
Minimum 16 (no concern about falling) to maximum 64 (severe concern about falling)
Time Frame
12 months
Title
Walking
Description
6-Minute Walk Test The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance (m) covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.
An increase in the distance walked indicates improvement in basic mobility.
Time Frame
12 months
Title
standing balance
Description
Standing balance will be estimated by the validated Stability Index for both right and left lower limb.
It evaluates proprioceptive control, visual dependence, and the risk of fall and injury.
The Stability Index is a score (0-100 %). 100% is high
Time Frame
12 months
Title
Muscle force
Description
Hand grip (KG)
Time Frame
12 months
Title
joint mobility
Description
Hip range of motion in degree, knee range of motion in degree, shoulder range of motion in degree
Time Frame
12 months
Title
Body Mass Index
Description
Weight and height will be combined to report BMI in kg/m^2
Time Frame
12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
signed informed consent
post menopausal women aged >40 years (with or without history of fractures, with or without pharmacological therapy for OP)
lumbar spine or femur T-score ≤-2,5
functional motor capacity normal or moderately reduced (Short Physical Performance Battery)
sedentary life style (having exercised less than 30 minutes per week in the last 6 months).
Exclusion Criteria are:
secondary OP49, impairment of communicative and/or sensorial functions so severe to make impossible understanding or executing trainer's instructions (dementia, aphasia, blindness, deafness);
heart failure (NYHA class >2);
unstable angina, pulmonary disease requiring oxygen therapy;
symptomatic peripheral arteriopathy;
myocardial infarction or hospital admission in the previous 6 months,
symptomatic orthostatic hypotension;
hypertension in poor pharmacologic control (diastolic >95 mmHg, systolic >160 mmHg),
previous implant of prosthesis at upper or lower limbs,
relevant neurological condition impairing motor or cognitive function, any other condition that the medical doctor (MD) considers to contraindicate the participation in an exercise program of moderate intensity.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudio Ripamonti
Organizational Affiliation
IOR
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istituto Ortopedico Rizzoli
City
Bologna
ZIP/Postal Code
40136
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
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Efficacy and Safety of the Physical Activity Program in Women With Post-menopausal Osteoporosis
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