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Exercise in the Elderly

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7001. Efficacy of Various Aerobic Exercises on Abdominal Obesity in Women With Metabolic Syndrome.

Start Date : August 1, 2016 Actual Primary Completion Date : April 1, 2018 Actual Study Completion Date : June 1, 2018 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Supervised treadmill group (%70 VO2 max) Supervised treadmill group (%70 VO2 max) (group 1): The participants were instructed walking exercise at their target heart rate, (% 70 of maximum oxygen consumption) on a treadmill in Sports (...) University Information provided by (Responsible Party): Füsun Ardıç, Pamukkale University Study Details Study Description Go to Brief Summary: Objective: To show metabolic and hormonal responses and effects on abdominal obesity of aerobic exercise in different intensity and duration and detraining period in women with metabolic syndrome. Condition or disease Intervention/treatment Phase Metabolic Syndrome Other: Supervised treadmill group (%70 VO2 max) (group 1) Other: Supervised treadmill group (%50 VO2

2018 Clinical Trials

7002. Effect of Huperzine A on Cognitive Function and Perception of Effort During Exercise

20 minutes per session, for at least six months prior to this study Exclusion Criteria: Anyone not within the age range listed in section 8a will be excluded. Individuals who require medical clearance to participate in vigorous exercise based on ACSM's risk assessment algorithm will be excluded from the study. The participant screening form will be used to identify signs and symptoms or medical conditions that require medical clearance to participate in vigorous exercise. Contacts and Locations (...) the first experimental session, and will receive the other substance during the second session. Condition or disease Intervention/treatment Phase Cognitive Enhancement During Exercise Other: Huperzine A Other: Placebo Early Phase 1 Detailed Description: Huperzine A improves cognitive function by inhibiting the enzyme acetylcholinesterase. This enzyme is responsible for the degradation of the neurotransmitter acetylcholine. inhibition of acetylcholinesterase may allow for greater availability

2018 Clinical Trials

7003. The Effect of Stabilization Exercises After Radiofrequency Lumbar Facet Denervation

with FJS after radiofrequency denervation. Condition or disease Intervention/treatment Phase Low Back Pain Facet Joint Pain Radiofrequency Denervation Pain Disability Physical Other: Exercise Not Applicable Detailed Description: Lumbar facet joint syndrome has been described as a potential cause of low back pain and affects an estimated 4% to 8% of those low back pain patients without neurological deficits or radiographic evidence of lumbar spine disease. The levels of physical performance (...) Baseline physical performance tests after radiofrequency denervation (at 2 week) and after exercise procedure (at 8 week) ] Eight physical performance tests (PPT) of daily activities such as climbing stairs, picking up something from the floor, bending forward, rolling up from supine position, putting on a sock, standing up from a lying position etc. were evaluated. The tests were observed by trained physiotherapist, who judged the patients' individual performance in each test using four grades

2018 Clinical Trials

7004. A Pilot Study of Motor Control Exercise and Patient Education for the Management of Chronic Low Back Pain in Rural Nigerian Community.

information Ages Eligible for Study: 18 Years to 65 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Male and female between 18 and 65 years old. Primary complaint of LBP experienced at least over the previous 3-month duration. Ability to read/understand English or Hausa language. Exclusion Criteria: Previous history of thoracic spine or lumbosacral spine surgery. Any neurological findings indicating radiculopathy. Evidence of serious (...) (CLBP) in a low resource rural Nigerian community. Condition or disease Intervention/treatment Phase Chronic Low Back Pain Behavioral: Motor Control Exercise Behavioral: Patient Education Not Applicable Detailed Description: This study will determine whether supervised exercise training emphasizing motor control exercise (MCE) approach and a designed patient education (PE) program based on the psychosocial approach will be feasible and acceptable in reducing pain intensity and functional disability

2018 Clinical Trials

7005. Home-based Arm and Hand Exercise to Improve Upper Limb Function After Traumatic Brain Injury

: January 17, 2018 Last Update Posted : February 27, 2019 See Sponsor: Kessler Foundation Information provided by (Responsible Party): Peii Chen, Kessler Foundation Study Details Study Description Go to Brief Summary: The purpose of this study is to find out whether the Home-based Arm and Hand Exercise (HAHE) program improves functions of the upper limb that is affected after traumatic brain injury. HAHE is made up of exercises that simulate real-life tasks. Condition or disease Intervention/treatment (...) Home-based Arm and Hand Exercise to Improve Upper Limb Function After Traumatic Brain Injury Home-based Arm and Hand Exercise to Improve Upper Limb Function After Traumatic Brain Injury - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more

2018 Clinical Trials

7006. A TSHRN1201 Sub-study-To Evaluate the Effects of add-on Ranolazine on Exercise Tolerance and Angina Frequency

Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 20 Years and older (Adult, Older Adult) Sexes Eligible for Study (...) : All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Male or female patients aged ≥ 20 years old. A minimum 3-month history of stable angina. Patients with diagnosis of coronary artery disease (CAD) via at least one of the following criteria: Angiographic evidence of ≥ 50% stenosis of ≥ 1 major coronary artery; CT angiographic evidence of ≥ 50% stenosis of ≥ 1 major coronary artery; History of previous myocardial infarction (MI)*; *Previous MI history of patients has to be occurred

2018 Clinical Trials

7007. Effect of Ivabradine on Exercise Capacity After Heart Transplantation

. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years to 100 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patients > 1 year post heart transplantation CAV verified by coronary angiography or intravascular ultrasound Resting HR > 80 bpm Age > 18 years Signed informed (...) that might per se influence exercise performance Known contraindication for treatment with ivabradine Hypersensitivity to the active substance or to any of the excipients of either study drug Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03405831

2018 Clinical Trials

7008. Home-Based Functional Exercise Program in Patients With Patellar Femoral Syndrome Over a 10-Week Period

: January 10, 2019 Sponsor: New York University School of Medicine Information provided by (Responsible Party): New York University School of Medicine Study Details Study Description Go to Brief Summary: The purpose of this study is to determine if a 10 week exercise rehabilitation program decreases anterior knee oain (PFPS) and improves function in patients with patellofemoral pain syndrome (PFPS). Individuals (age 18-50) with PFPS will be recruited to participate in this study to see if a 10 week (...) exercise program focusing in core and hip strengthening, lower extremity strengthening foot intrinsic strengthening can decrease pain and increase function. Condition or disease Intervention/treatment Phase Patellar Femoral Syndrome Behavioral: 10 Week Exercise Program Behavioral: DVD Program After 10 Weeks Not Applicable Detailed Description: Patellofemoral pain syndrome (PFPS) is a very prevalent condition that presents in great number to patients in physician's offices and has a high recurrence rate

2018 Clinical Trials

7009. Whole Body Exercise in Spinal Cord Injury: Effects on Psychosocial Function

the barriers to intense exercise. The investigators will use hybrid functional electrical stimulation row training (FESRT) to allow for a more intense exercise stimulus, potentially having a greater impact on psychosocial wellbeing. There is initial evidence that persons with mobility impairments who are highly physically active demonstrate better psychosocial wellbeing compared with those who have low levels of physical activity. A limitation to understanding the influence of exercise on psychosocial (...) , you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Adults (>18 years of age) Be in good health (asymptomatic for acute treatable illness) and medically cleared to exercise Own an iPhone or Android smartphone with the capacity to download

2018 Clinical Trials

7010. Patient Activation Through Counseling, Exercise and Mobilization

: Supportive Care Official Title: Engaging the Older Cancer Patient; Patient Activation Through Counseling, Exercise and Mobilization - Pancreatic, Biliary Tract, and Lung Cancer (PACE-Mobil-PBL) - a Randomized Controlled Trial Actual Study Start Date : April 4, 2018 Estimated Primary Completion Date : December 31, 2019 Estimated Study Completion Date : May 1, 2021 Resource links provided by the National Library of Medicine related topics: related topics: resources: Arms and Interventions Go to Arm (...) , and to provide a signed informed consent form. Exclusion Criteria, patients with: Small-cell lung cancer. Any physical condition that hinder the execution of physical exercise training. Documented and uncontrolled brain metastases that hinder participation in an exercise-based trial, based on the referring oncologist's assessment. Dementia, psychotic disorders, or other cognitive diseases or conditions that hinder participation in a clinical exercise-based trial. Unstable medical disease or history

2018 Clinical Trials

7011. Physiotherapeutic Scoliosis Specific Exercises As Treatment for Adult Degenerative Scoliosis

low back physical therapy (PT). Condition or disease Intervention/treatment Phase Degenerative Scoliosis Behavioral: Physiotherapeutic Scoliosis Specific Exercises (PSSE) Behavioral: Conventional Physical Therapy (PT) Not Applicable Detailed Description: Adult scoliosis with chronic back pain is a very complex condition. Chronic back pain remains one of our country's most costly conditions to manage and treat. Many of these patients have difficulty with activities of daily living (ADL), household (...) Posted : January 29, 2018 Last Update Posted : January 29, 2018 See Sponsor: Columbia University Information provided by (Responsible Party): Allen Chen, Columbia University Study Details Study Description Go to Brief Summary: This is a pilot study to lead to a larger prospective, randomized, controlled study of older adult (ages 50 and older) spinal patients with thoracolumbar/lumbar scoliosis evaluating improvement with physiotherapeutic scoliosis-specific exercise (PSSE) compared to traditional

2018 Clinical Trials

7012. Exercise and Weight Control

activity after the intervention has ceased. Condition or disease Intervention/treatment Phase Obesity Exercise Reinforcement Behavioral: Exercise Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 60 participants Allocation: Randomized Intervention Model: Factorial Assignment Intervention Model Description: Baseline demographic and physical characteristics will be reported as means and standard errors. Baseline group (...) to determine each individual's level of compensation, termed compensation index. Predictors of compensation index that will be assessed will include hunger/satiety hormone concentrations at rest and in response to a meal, reward driven feeding, changes in metabolic rate, and energy intake throughout the intervention. Exercise reinforcement and physical activity will also be assessed as a separate aim to determine if exercise reinforcement can be increased and if this can promote greater habitual physical

2018 Clinical Trials

7013. Cartilage Adaptation and Response to Interleukins and Exercise

for eligibility information Ages Eligible for Study: 40 Years to 90 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Primary osteoarthritis of the knee scheduled for knee replacement surgery Must be able to perform physical exercise Age 40-90 years old BMI 18.5-40 kg/m^2 None smoker for the last 6 weeks Exclusion Criteria: Regular intake of: non steroid anti-inflammatory drugs (NSAID) corticoid-steroids disease modifying anti-rheumatic drugs (...) Mongy Jørgensen, MD, Bispebjerg Hospital Study Details Study Description Go to Brief Summary: This study will examine the effect of exercise on the turnover of collagen in articular cartilage and the content of cytokines in the synovial fluid from human adults with osteoarthritis. Condition or disease Intervention/treatment Phase Osteo Arthritis Knee Behavioral: Exercise. Not Applicable Detailed Description: By using stabile isotope labelling, this study will track the formation and destination

2018 Clinical Trials

7014. Exercise Activity-Based Bolus Decisions in Type 1 Diabetes

bolusing to compensate for significant activity (e.g. marathon runner who uses temporary basal rates routinely and has separate basal profiles to account for exercise) Inability to be physically active for more than 30 minutes per day. Current enrollment in another intervention clinical trial. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided (...) Exercise Activity-Based Bolus Decisions in Type 1 Diabetes Exercise Activity-Based Bolus Decisions in Type 1 Diabetes - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Exercise Activity-Based Bolus Decisions

2018 Clinical Trials

7015. Effectiveness Chronic Kidney Disease & Therapeutic Exercise

outcome) is measured at baseline and 1 month after treatment start. Condition or disease Intervention/treatment Phase Kidney Diseases Exercise Other: Therapeutic Exercise Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 70 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Outcomes Assessor) Primary Purpose: Treatment Official Title: Effectiveness and Safety (...) table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patients with chronic kidney disease Exclusion Criteria: Cognitive impairment and non signed consent inform form Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information

2018 Clinical Trials

7016. Efficacy of Three-dimensionally Integrated Exercise for Scoliosis in Patients With Adolescent Idiopathic Scoliosis

. It is recommended that the physiotherapeutic scoliosis-specific exercises should be the first step to treat idiopathic scoliosis to prevent/limit progression of the deformity. Three-dimensionally integrated exercise for scoliosis is based the theory of physiotherapeutic scoliosis specific exercises, and consists of patient education, 3-dimension self-correction, stabilization of the corrected posture and training activity of daily living, combined with neuro-motor control, proprioceptive training, balance (...) , sagittal profile and health related quality-of-life. Condition or disease Intervention/treatment Phase Scoliosis,Idiopathic,Adolescent Behavioral: observation Behavioral: three-dimensionally integrated exercise for scoliosis Not Applicable Detailed Description: Adolescent idiopathic scoliosis (AIS) is one of the most prevalent spinal deformity that may progress sharply during growth. According to the severity of the curve, the major treatment approaches for patient with AIS include exercises, bracing

2018 Clinical Trials

7017. Periodization of Exercise Training in Patients With Coronary Heart Disease.

about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria for patients with coronary heart disease: Major Adequate physical and mental capacities Autonomy in daily activities Documented (...) . Periodization of Exercise Training in Patients With Coronary Heart Disease. (PERIOD) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03443193 Recruitment Status : Active, not recruiting First Posted : February 23, 2018 Last Update Posted : February 23, 2018 Sponsor: Montreal Heart Institute Information

2018 Clinical Trials

7018. Aerobic Exercise and Inhibitory Control

behaviours, physical activity levels, urges to smoke, and inhibitory control. Phase II will consist of a 12-hour smoking abstinence period conducted at home, followed by reassessment of urges to smoke and inhibitory control. Participants will then be randomized to either 20 minutes of aerobic exercise or sitting. Following the intervention, reassessment of urges to smoke, inhibitory control, and time to first cigarette smoked will be conducted. Condition or disease Intervention/treatment Phase Smoking (...) Estimated Primary Completion Date : December 2018 Estimated Study Completion Date : March 2019 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Exercise Aerobic exercise intervention Behavioral: Exercise 20 minutes of aerobic exercise (walking on a treadmill) at 2/3 of participant's maximum heart rate (maximum heart rate calculated as 220-age). Active Comparator: Non-Exercise Non-aerobic exercise

2018 Clinical Trials

7019. The Altered Immune Response to Exercise in Patients With Fibromyalgia Before and After a Mind-body Intervention

. The QOLS is a 15-item questionnaire that accesses five conceptual domains of quality of life: material and physical well-being, relationships with other people, social, community and civic activities, personal development and fulfillment, and recreation. This scale has been shown to be reliable and validated by previous studies Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor (...) Identifier: NCT03441997 Recruitment Status : Recruiting First Posted : February 22, 2018 Last Update Posted : January 4, 2019 See Sponsor: University of Kansas Medical Center Information provided by (Responsible Party): University of Kansas Medical Center Study Details Study Description Go to Brief Summary: The purpose of this study is to compare two different exercise programs to see if there are differences after exercise in fibromyalgia (FM) symptoms and responses from the immune system. Condition

2018 Clinical Trials

7020. Effects Of The Core Stability Exercises On Balance And Hand Functions

of the center of gravity in the space changes frequently with the movement of the body segments. Postural adjustments that required to restore the impaired balance due to this displacement of center of gravity, consist of lumbal stabilization with the activation of the core muscles. The upper extremity is a body part with a wide variety of abilities. With the same basic anatomical structures, the arms, forearms, hands and fingers may function differently. The upper extremity is the primary tool that people (...) of this study planned in line with the available information is to investigate the effect of core stabilization exercises applied for 6 weeks on body balance and hand functions. Condition or disease Intervention/treatment Phase Healthy Other: Exercise Not Applicable Detailed Description: The core region is prescribed as a box which is formed from abdominal muscles at the front, paraspinals and glutueal muscles on the back, diaphragm on the roof, oblique abdominal muscles on sides and hip joint and pelvic

2018 Clinical Trials

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