ObesityBaSEIBNCT02843048
Bariatric Surgery and Exercise Bone Trial
A study testing Exercise training program and Standard medical care in people with Obesity and Metabolic Bone Disease, run by Universidade do Porto at 1 site in Portugal.
Trial summary
Despite being effective in weight reduction in severely obese patients, bariatric surgery (BS) negatively influences bone metabolism and increases the risk of falls thereby potentially increasing the risk of fracture. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Obesity, Metabolic Bone Disease, Accidental Falls
- What is being tested?
- Exercise training program and Standard medical care
- Type of treatment
- Injection or infusion, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 86 participants
- Where
- 1 sitePortugal
- Study dates
- Apr 2016to Mar 2019
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- meet the referral criteria for bariatric surgery;
- BMI >40 kg.m-2 or >35 kg.m-2 with obesity-related comorbidities;
- Motivation to participate in the study, regardless to the allocation group
Who cannot join
- use of drugs that interfere with bone metabolism (i.e. bisphosphonates, teriparatide, calcitonin, hormone replacement therapy, chronic use of corticosteroids, thiazide diuretics);
- Unable to perform exercise of moderate intensity;
- Health condition that could be aggravated by exercise (i.e. uncontrolled arterial hypertension, severe kidney disease, class III New York Heart Association heart failure);
- Peri-menopausal status with last menstruation <1 year;
- Known metabolic bone disease (i.e. Osteogenesis Imperfecta, Paget bone disease);
- Concurrent participation in a structured exercise program (>30 min in duration >1 day/week);
- Pregnancy or breast-feeding
Trial locations and contacts
1 site in 1 country.
About this study
Official title: BaSEIB Clinical Trial - Bariatric Surgery and Exercise Intervention Bone Trial
Despite being effective in weight reduction in severely obese patients, bariatric surgery (BS) negatively influences bone metabolism and increases the risk of falls thereby potentially increasing the risk of fracture. The mechanisms of BS induced bone loss are unknown but may be related to calcium and vitamin D malabsorption, changes in the energy regulation metabolism and gastrointestinal hormonal physiology. Since the etiology of BS induced bone loss is largely unknown, treatment relies mostly on calcium and vitamin D supplementation, which provide little benefit.
Exercise is an effective strategy to prevent bone mass losses in several health conditions. However, no study so far has examined the effects of an exercise-training program in the prevention of BS induced bone loss. The investigators main goal is to investigate the effects on bone metabolism and fracture risk of an exercise-training program specifically tailored to improve bone health and balance of patients that underwent BS. The investigators will perform a randomized controlled trial on obese patients (n=80; BMI>40 Kg.m-2) elected to BS. Patients will be randomly assigned into 2 groups i) a group receiving standard follow-up and medical care, or ii) a group that will undergo a 11 months' Exercise Training program designed to improve bone health and reduce fall risk plus the standard follow-up and medical care. All patients will be assessed i) before the surgery, ii) one month, iii) 6 months, and iv) 12 months after the surgery. Assessments include: biochemical markers of bone turnover (BTM), BMD, bone tissue biomechanical properties, hormones involved in the regulation of energy, gastrointestinal and bone metabolism, body composition, BMI, nutritional intake, balance, muscle strength, cardiorespiratory fitness and daily physical activity. These evaluations will allow the investigators to understand the effects of an exercise-training program on bone metabolism of BS patients, contributing also to further elucidate the mechanisms underlying BS induced bone loss and fracture risk increase. The investigators will use established methods in the literature as well as novel procedures, which will enable them to overcome some of the limitations of previous studies. At the end of the study the investigators expect to have collected consistent data about whether an exercise-training program is or is not able to effectively prevent BS induced bone losses and fracture risk increases.
Read the detailed description
The investigators main goal is to determine if an Exercise-Training Intervention program (ETI) tailored to improve bone health, strength and balance, is effective in preventing Roux-en-Y gastric bypass (RYGB) induced fracture risk. To achieve this the investigators will perform a randomized clinical trial (RCT) on volunteer obese patients (BMI>35 Kg.m-2) undergoing RYGB that will be followed for 13-months (Figure 1). The patients will be recruited, operated and will receive follow-up medical care in the Department of General Surgery from the Centro Hospitalar de São João E.P.E (DSHSJ). After being elected for RYGB and if inclusion and exclusion criteria are met, patients who decide to join the study will be randomly assigned to either i) participate in a 11 months duration ETI tailored to improve bone health and reduce fall risk in addition to the standard follow-up medical care (MFU) (ETI+MFU group), or ii) will receive only MFU (control group). Recruiting patients from only one institution will increase the likelihood of all patients receiving the same surgical and MFU care, reducing the bias related to the use of different clinical protocols. The option to include only RYGB is also to reduce the bias associated with the surgical technique. Participants allocated to the ETI+MFU group will undergo an exercise-training program of 11 months duration, 3 sessions/week, and 60 minutes/session, starting one month after the surgery. Each exercise session will be supervised and will include 5 major components: i) warm-up, ii) multidirectional jumps, iii) balance, iv) strength and, v) cool down. This structure is planned to meet two main objectives: i) enhance bone formation and, ii) reduce fall risk by improving muscle strength, cardiorespiratory fitness and balance. The ETI will last almost 1 year because the effects of BS on bone metabolism have been shown to be greatest during the first postoperative year (1). As the investigators main objective is to understand, in a broad perspective, the possible therapeutic benefits that an ETI has on the BS patient bone health and fracture risk, the plan is to investigate several variables in this study (bone turnover markers, bone mineral content (BMC) and density (BMD), body composition, body mass index (BMI), nutritional intake, static balance, dynamic balance, muscle strength of the lower limbs and trunk, daily physical activity, cardiorespiratory fitness, bone derived hormones, hormones involved in phosphate and calcium metabolism, adipokines, gastrointestinal and energy-metabolism hormones and gonadal hormones). These will enable the investigators to comprehensively understand the metabolic changes following BS that might affect bone health, and how can exercise influence those changes potentially preventing fracture risk increases.
Each patient will be assessed 4 times during the study (Figure 1). Each assay will match the monitoring protocols already scheduled by the DSHSJ for all patients undergoing BS. The 1st evaluation will occur prior to BS, to gather pre-surgical state. The 2nd, 3rd and 4th evaluations will occur in the 1st (before the beginning of the exercise-training program for the patients allocated to the exercise intervention group), 6th and 12th months after bariatric surgery, respectively. The variables analyzed at each time point fit into four major categories: i) bone quality surrogates (BTM, BMD, bone biomechanical properties); ii) anthropometry (weight, height, body composition, nutritional intake; iii) fall risk (static and dynamic balance, muscle strength, cardiorespiratory fitness, daily physical activity), iv) hormones involved in calcium, bone and gastro-intestinal metabolism. Biochemical analysis will be performed in blood samples collected during follow up hospital visits. Biochemical markers of bone turnover (BTM) reflect the degree of bone remodeling and the balance between formation and resorption and are therefore surrogates of fracture risk. As BS profoundly affects body composition, gastrointestinal and energy-regulation physiology, and because adipose tissue and gut-associated hormones also influence bone metabolism, the investigators will determine how these hormones are affected by RYGB and exercise. By monitoring these variables the investigators will gain insight on the etiological mechanisms associated with BS induced bone loss and the therapeutic effects of exercise. BS also leads to a reduction in calcium and vitamin D absorption, which may result in increased bone resorption. The investigators will therefore also monitor Vitamin D, Parathyroid Hormone (PTH), calcium and phosphorous concentrations to determine how they are influenced by the ETI. Despite mechanical unloading due to the weight loss may contribute to bone loss following BS, there is no data supporting this mechanism. To investigate this relation, the investigators will also monitor serum sclerostin, a protein released by osteocytes in response to mechanical unloading that negatively regulates bone formation. To determine the effects of BS and exercise on skeletal muscle and adipose tissue mass, the investigators will measure body composition and BMI in all patients. As one of the investigators main goal is to investigate the effects of the ETI on fall risk, they also plan to determine the cardiorespiratory fitness and muscle strength in these patients since these variables have been previously shown to influence fall risk. Daily physical activity and nutritional intake will also be determined by accelerometer and food diary, respectively, in order to control for confounding variables. Despite the several caveats associated with the determination of BMD by DXA, the investigators plan to analyze this variable, as it will provide data that will enable them to compare their results with the results from previous studies. Nevertheless, the investigators plan to complement this information with the direct assessment of bone biomechanical properties, which until recently was only available in in vitro studies due to the invasive nature of the procedure. Bone micro-indentation is a newer technique that allows measuring bone tissue mechanical properties in the clinical setting, which reflects with higher accuracy the bone resistance to fracture (6). One of the main outcomes in this research is to investigate the effects of BS on fall risk, as there is almost no data on this issue. This will be accomplished by direct determination of static and dynamic balance by means of using a forces platform. By analyzing this broad set of parameters the investigators plan to contribute with a more thorough understanding of the effects of BS on bone metabolism and, most importantly, how can an exercise training program, specifically tailored to improve bone health and balance, can reduce the risk of bone fractures in these patients. Only by analyzing this broad number of parameters will the investigators be able to control the several confounding variables and gain deeper insight into the effects of BS and exercise on the bone metabolism of these patients, thereby contributing with a potently useful strategy for the management of skeletal health in BS patients.
- Conditions
- Obesity, Metabolic Bone Disease, Accidental Falls
- Being tested
- Exercise training program, Standard medical care
- Keywords
- Osteoporosis, Bariatric Surgery, Physical exercise, Obesity
- Medical subject headings
- Obesity, Bone Diseases, Metabolic, Osteoporosis, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Exercise training programBehavioural
Participants allocated to the "Exercise training plus standard medical care" group will undergo an exercise-training program of 11 months duration, 3 sessions/week, and 60 minutes/session, starting one month after the surgery. Each exercise session will be supervised and will include 5 major components: i) warm-up, ii) multidirectional jumps, iii) balance, iv) strength and, v) cool down. This structure is planned to meet two main objectives: i) enhance bone formation and, ii) reduce fall risk by improving muscle strength, cardiorespiratory fitness and balance.
Standard medical careBehavioural
Standard follow-up medical care following bariatric surgery
| Study group | Role | What they receive |
|---|---|---|
| Exercise training | Experimental | Exercise training plus standard medical follow-up care Receives: Behavioral: Exercise training program |
| Standard medical care | Active comparator | Standard medical follow-up care only Receives: Behavioral: Standard medical care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Bone mineral density
Assayed by dual energy x-ray absorptiometry (DXA); g/cm2
Measured: 12 months
Biochemical marker of bone resorption
Collagen type 1 cross-linked C-telopeptide (CTX; ng/mL)
Measured: 12 months
Bone Material Strength index (BMSi)
Normalized parameter of bone material's resistance to indentation (OsteoProbe RUO)
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Jul 2016 (estimated)
- Study startApr 2016
- Primary completionMar 2018 (estimated)
- Study completionMar 2019 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for ObesityStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 86 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universidade do Porto
- Sponsor type
- University, hospital or other
- Collaborators
- Centro Hospitalar De São João, E.P.E., Fundação para a Ciência e a Tecnologia
- Responsible party
- Principal investigator, Hélder Fonseca, Universidade do Porto
- Investigators
- Hélder Fonseca, PhD, Principal investigator, CIAFEL
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02843048
- Sponsor's protocol ID
- PTDC/DTP-DES/0968/2014
- Other IDs
- POCI-01-0145-FEDER-016707
- Acronym
- BaSEIB
- Status last verified
- Oct 2017
- First submitted
- 14 Jul 2016
- Last updated
- 31 Oct 2017
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Publications
Boppre G, Diniz-Sousa F, Veras L, Bezerra A, Devezas V, Preto J, Santos-Sousa H, Oliveira J, Fonseca H. Impact of a Multicomponent Exercise Training Program on Muscle Strength After Bariatric Surgery: A Randomized Controlled Trial. Obes Surg. 2024 May;34(5):1704-1716. doi: 10.1007/s11695-024-07173-w. Epub 2024 Mar 27.
PubMed 38532144
Study at a glance
From the registry record, last updated by the sponsor on 31 Oct 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- BaSEIB Clinical Trial - Bariatric Surgery and Exercise Intervention Bone Trial
- ClinicalTrials.gov ID
- NCT02843048
- Acronym / sponsor ID
- BaSEIB / PTDC/DTP-DES/0968/2014
- Conditions
- Obesity, Metabolic Bone Disease, Accidental Falls
- Keywords
- Osteoporosis, Bariatric Surgery, Physical exercise, Obesity
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 86 participants (actual)
- Lead sponsor
- Universidade do PortoUniversity, hospital or other
- Collaborators
- Centro Hospitalar De São João, E.P.E., Fundação para a Ciência e a Tecnologia
- Study start
- Apr 2016
- Primary completion
- Mar 2018 (estimated)
- Study completion
- Mar 2019 (estimated)
- First posted
- 25 Jul 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Despite being effective in weight reduction in severely obese patients, bariatric surgery (BS) negatively influences bone metabolism and increases the risk of falls thereby potentially increasing the risk of fracture. The mechanisms of BS induced bone loss are unknown but may be related to calcium and vitamin D malabsorption, changes in the energy regulation metabolism and gastrointestinal hormonal physiology. Since the etiology of BS induced bone loss is largely unknown, treatment relies mostly on calcium and vitamin D supplementation, which provide little benefit.
Exercise is an effective strategy to prevent bone mass losses in several health conditions. However, no study so far has examined the effects of an exercise-training program in the prevention of BS induced bone loss. The investigators main goal is to investigate the effects on bone metabolism and fracture risk of an exercise-training program specifically tailored to improve bone health and balance of patients that underwent BS. The investigators will perform a randomized controlled trial on obese patients (n=80; BMI>40 Kg.m-2) elected to BS. Patients will be randomly assigned into 2 groups i) a group receiving standard follow-up and medical care, or ii) a group that will undergo a 11 months' Exercise Training program designed to improve bone health and reduce fall risk plus the standard follow-up and medical care. All patients will be assessed i) before the surgery, ii) one month, iii) 6 months, and iv) 12 months after the surgery. Assessments include: biochemical markers of bone turnover (BTM), BMD, bone tissue biomechanical properties, hormones involved in the regulation of energy, gastrointestinal and bone metabolism, body composition, BMI, nutritional intake, balance, muscle strength, cardiorespiratory fitness and daily physical activity. These evaluations will allow the investigators to understand the effects of an exercise-training program on bone metabolism of BS patients, contributing also to further elucidate the mechanisms underlying BS induced bone loss and fracture risk increase. The investigators will use established methods in the literature as well as novel procedures, which will enable them to overcome some of the limitations of previous studies. At the end of the study the investigators expect to have collected consistent data about whether an exercise-training program is or is not able to effectively prevent BS induced bone losses and fracture risk increases.
Detailed description
The investigators main goal is to determine if an Exercise-Training Intervention program (ETI) tailored to improve bone health, strength and balance, is effective in preventing Roux-en-Y gastric bypass (RYGB) induced fracture risk. To achieve this the investigators will perform a randomized clinical trial (RCT) on volunteer obese patients (BMI>35 Kg.m-2) undergoing RYGB that will be followed for 13-months (Figure 1). The patients will be recruited, operated and will receive follow-up medical care in the Department of General Surgery from the Centro Hospitalar de São João E.P.E (DSHSJ). After being elected for RYGB and if inclusion and exclusion criteria are met, patients who decide to join the study will be randomly assigned to either i) participate in a 11 months duration ETI tailored to improve bone health and reduce fall risk in addition to the standard follow-up medical care (MFU) (ETI+MFU group), or ii) will receive only MFU (control group). Recruiting patients from only one institution will increase the likelihood of all patients receiving the same surgical and MFU care, reducing the bias related to the use of different clinical protocols. The option to include only RYGB is also to reduce the bias associated with the surgical technique. Participants allocated to the ETI+MFU group will undergo an exercise-training program of 11 months duration, 3 sessions/week, and 60 minutes/session, starting one month after the surgery. Each exercise session will be supervised and will include 5 major components: i) warm-up, ii) multidirectional jumps, iii) balance, iv) strength and, v) cool down. This structure is planned to meet two main objectives: i) enhance bone formation and, ii) reduce fall risk by improving muscle strength, cardiorespiratory fitness and balance. The ETI will last almost 1 year because the effects of BS on bone metabolism have been shown to be greatest during the first postoperative year (1). As the investigators main objective is to understand, in a broad perspective, the possible therapeutic benefits that an ETI has on the BS patient bone health and fracture risk, the plan is to investigate several variables in this study (bone turnover markers, bone mineral content (BMC) and density (BMD), body composition, body mass index (BMI), nutritional intake, static balance, dynamic balance, muscle strength of the lower limbs and trunk, daily physical activity, cardiorespiratory fitness, bone derived hormones, hormones involved in phosphate and calcium metabolism, adipokines, gastrointestinal and energy-metabolism hormones and gonadal hormones). These will enable the investigators to comprehensively understand the metabolic changes following BS that might affect bone health, and how can exercise influence those changes potentially preventing fracture risk increases.
Each patient will be assessed 4 times during the study (Figure 1). Each assay will match the monitoring protocols already scheduled by the DSHSJ for all patients undergoing BS. The 1st evaluation will occur prior to BS, to gather pre-surgical state. The 2nd, 3rd and 4th evaluations will occur in the 1st (before the beginning of the exercise-training program for the patients allocated to the exercise intervention group), 6th and 12th months after bariatric surgery, respectively. The variables analyzed at each time point fit into four major categories: i) bone quality surrogates (BTM, BMD, bone biomechanical properties); ii) anthropometry (weight, height, body composition, nutritional intake; iii) fall risk (static and dynamic balance, muscle strength, cardiorespiratory fitness, daily physical activity), iv) hormones involved in calcium, bone and gastro-intestinal metabolism. Biochemical analysis will be performed in blood samples collected during follow up hospital visits. Biochemical markers of bone turnover (BTM) reflect the degree of bone remodeling and the balance between formation and resorption and are therefore surrogates of fracture risk. As BS profoundly affects body composition, gastrointestinal and energy-regulation physiology, and because adipose tissue and gut-associated hormones also influence bone metabolism, the investigators will determine how these hormones are affected by RYGB and exercise. By monitoring these variables the investigators will gain insight on the etiological mechanisms associated with BS induced bone loss and the therapeutic effects of exercise. BS also leads to a reduction in calcium and vitamin D absorption, which may result in increased bone resorption. The investigators will therefore also monitor Vitamin D, Parathyroid Hormone (PTH), calcium and phosphorous concentrations to determine how they are influenced by the ETI. Despite mechanical unloading due to the weight loss may contribute to bone loss following BS, there is no data supporting this mechanism. To investigate this relation, the investigators will also monitor serum sclerostin, a protein released by osteocytes in response to mechanical unloading that negatively regulates bone formation. To determine the effects of BS and exercise on skeletal muscle and adipose tissue mass, the investigators will measure body composition and BMI in all patients. As one of the investigators main goal is to investigate the effects of the ETI on fall risk, they also plan to determine the cardiorespiratory fitness and muscle strength in these patients since these variables have been previously shown to influence fall risk. Daily physical activity and nutritional intake will also be determined by accelerometer and food diary, respectively, in order to control for confounding variables. Despite the several caveats associated with the determination of BMD by DXA, the investigators plan to analyze this variable, as it will provide data that will enable them to compare their results with the results from previous studies. Nevertheless, the investigators plan to complement this information with the direct assessment of bone biomechanical properties, which until recently was only available in in vitro studies due to the invasive nature of the procedure. Bone micro-indentation is a newer technique that allows measuring bone tissue mechanical properties in the clinical setting, which reflects with higher accuracy the bone resistance to fracture (6). One of the main outcomes in this research is to investigate the effects of BS on fall risk, as there is almost no data on this issue. This will be accomplished by direct determination of static and dynamic balance by means of using a forces platform. By analyzing this broad set of parameters the investigators plan to contribute with a more thorough understanding of the effects of BS on bone metabolism and, most importantly, how can an exercise training program, specifically tailored to improve bone health and balance, can reduce the risk of bone fractures in these patients. Only by analyzing this broad number of parameters will the investigators be able to control the several confounding variables and gain deeper insight into the effects of BS and exercise on the bone metabolism of these patients, thereby contributing with a potently useful strategy for the management of skeletal health in BS patients.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Exercise training | Experimental | Behavioral: Exercise training programExercise training plus standard medical follow-up care |
| Standard medical care | Active comparator | Behavioral: Standard medical careStandard medical follow-up care only |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- meet the referral criteria for bariatric surgery;
- BMI >40 kg.m-2 or >35 kg.m-2 with obesity-related comorbidities;
- Motivation to participate in the study, regardless to the allocation group
Key exclusion criteria (7 listed)
- use of drugs that interfere with bone metabolism (i.e. bisphosphonates, teriparatide, calcitonin, hormone replacement therapy, chronic use of corticosteroids, thiazide diuretics);
- Unable to perform exercise of moderate intensity;
- Health condition that could be aggravated by exercise (i.e. uncontrolled arterial hypertension, severe kidney disease, class III New York Heart Association heart failure);
- Peri-menopausal status with last menstruation <1 year;
- Known metabolic bone disease (i.e. Osteogenesis Imperfecta, Paget bone disease);
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Exercise training programParticipants allocated to the "Exercise training plus standard medical care" group will undergo an exercise-training program of 11 months duration, 3 sessions/week, and 60 minutes/session, starting one month after the surgery. Each exercise session will be supervised and will include 5 major components: i) warm-up, ii) multidirectional jumps, iii) balance, iv) strength and, v) cool down. This structure is planned to meet two main objectives: i) enhance bone formation and, ii) reduce fall risk by improving muscle strength, cardiorespiratory fitness and balance. | Behavioural | Exercise training |
| Standard medical careStandard follow-up medical care following bariatric surgery | Behavioural | Standard medical care |
Primary outcome
Bone mineral density
Time frame: 12 months
Assayed by dual energy x-ray absorptiometry (DXA); g/cm2
Biochemical marker of bone resorption
Time frame: 12 months
Collagen type 1 cross-linked C-telopeptide (CTX; ng/mL)
Bone Material Strength index (BMSi)
Time frame: 12 months
Normalized parameter of bone material's resistance to indentation (OsteoProbe RUO)
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Oct 2017.
- Derived from this study: PubMed 38532144Boppre G, Diniz-Sousa F, Veras L, Bezerra A, Devezas V, Preto J, Santos-Sousa H, Oliveira J, Fonseca H. Impact of a Multicomponent Exercise Training Program on Muscle Strength After Bariatric Surgery: A Randomized Controlled Trial. Obes Surg. 2024 May;34(5):1704-1716. doi: 10.1007/s11695-024-07173-w. Epub 2024 Mar 27.
- Project home pageLink provided by the sponsor.
- Individual participant dataSharing planned: No
Related trials for Obesity
Active, not recruiting
Comparing 150cm OAGB With 150cm Biliopancreatic Limb RYGB. A Non-inferiority Trial
Bariatric Surgery Candidate, Obesity
RecruitingPhase 3
Maridebart Cafraglutide in Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity
Heart Failure With Preserved Ejection Fraction, Heart Failure With Mildly Reduced Ejection Fraction
Not yet recruitingPhase 1
A Study of Safety of SUN-0864 and How it is Processed by and Affects the Body in Healthy Adults and Healthy Adults Who Are Overweight or Obese.
Healthy Participants
Not yet recruiting
Evaluation of the Axomove Therapy Medical Device to Facilitate Adapted Physical Activity for Patients With Obesity
Obese Adults
Not yet recruiting
Efficacy, Safety, and Treatment Satisfaction of Once-Weekly Tirzepatide in Obese Type 2 Diabetic Patients
Type 2 Diabetes Mellitus (T2DM), Obesity, Overweight
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Hélder Fonseca, PhD principal investigator
CIAFEL
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Exercise training program and Standard medical care in people with Obesity and Metabolic Bone Disease, run by Universidade do Porto at 1 site in Portugal.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 31 Oct 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Portugal. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Bone mineral density (time frame: 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02843048, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Oct 2017.