Postmenopausal Osteopenia Clinical Trial
Official title:
Effects of Kinect-based Virtual Reality Training on Bone Mineral Density, Fracture Risk, Physical Performance and Quality of Life in Postmenopausal Women With Osteopenia
Verified date | November 2023 |
Source | Riphah International University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Osteopenia is a clinical term to define the declined Bone Mineral Density (BMD) as per the normal reference values but not low enough to meet osteoporotic diagnostic criteria. A Dual-energy x-ray absorptiometry (DXA) bone scan is used to diagnose decreased BMD. Osteopenia is, as described by the World Health Organization (WHO), a score ranging from -1 to -2.5, whereas Osteoporosis is diagnosed with values less than - 2.5. The risk of a decrease in BMD doubles as a woman goes into Menopause. The objective of this study will be to determine the effects of Kinect-based virtual reality training on BMD, fracture risk, physical function and Quality of life in postmenopausal women with Osteopenia. This study will be a Randomized controlled trial. The study will be conducted at Riphah Rehabilitation Center, Lahore. Duration of the study will be 18 months. The sample size will be calculated after the completion of the pilot study. Initial screening of the participants will be done as per screening protocol and participants fulfilling inclusion criteria will be randomly allocated into two groups. Group A will receive Kinect based virtual reality training along with routine diet and routine Medication. Group B will be controlled with routine diet and routine Medication. Participants of both groups will be assessed at baseline for BMD, risk of fracture, all Objective and subjective parameters of Physical Performance and Quality of Life. Post-treatment assessment of Physical performance measures and Quality of life will be done after the 12th and 24th week, while BMD and fracture risk will be measured only after the 24th week. BMD will be measured by Dual-Energy X-ray Absorptiometry (DEXA) for Lumbar spine (BMD), proximal femur (BMD), T-score and Z-score. Fracture risk will be calculated by FRAX score, which estimates a fracture's probability within the next ten years. Physical Performance will be assessed by Time Up and Go Test (TUG), Functional Reach Test, Five Times Sit to Stand Test, Grip strength, Fall Efficacy Scale International, Borg revised category-ratio scale (0 to 10 scale) and Dyspnea index. Urdu Version of ECOS-16 will be used for the evaluation of health-related Quality of life (HRQOL). Data will be analyzed on SPSS-25.
Status | Completed |
Enrollment | 52 |
Est. completion date | June 15, 2023 |
Est. primary completion date | June 1, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 48 Years to 70 Years |
Eligibility | Inclusion Criteria: - Postmenopausal women - Osteopenia verified by dual-energy X-ray absorptiometry with Lumbar spine or femur T-score between -1 to -2.5 either recommended by the study investigators or verified by a physician in the past one year. - current body mass index (BMI) < 30 kg/m2 - Patients with Normal balance and no risk of fall checked by Tandem Stance Test (TST) Exclusion Criteria: - Impairment of communicative and sensorial functions, Impaired Cognition, and Neurological disorders - Cardiovascular disease or other chronic conditions that could interfere with their safety during testing or training procedures - Pulmonary disease requiring oxygen therapy, Symptomatic orthostatic hypotension, Moderate or severe respiratory failure - secondary osteoporosis, arthrosis or known osteoporotic fractures, neoplastic disease - Virtual game phobia - Games used in past six months - Cases with epilepsy |
Country | Name | City | State |
---|---|---|---|
Pakistan | Genesis Healthcare Consultants | Lahore | Punjab |
Pakistan | Riaz | Lahore | Punjab |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | DUAL-ENERGY X-RAY ABSORPTIOMETRY (DXA) | The most commonly used Gold standard BMD test is a densitometric technique called DXA (dual-energy X-ray absorptiometry), which can be measured in vivo and validated by many studies for BMD, T-score and Z-Score. | 6 Months | |
Primary | WHO's FRACTURE RISK ASSESSMENT TOOL (FRAX) ALGORITHM | FRAX, released in 2008 by the World Health Organization, was developed and validated under the direction of Professor John Kanis with the support of many individuals and organizations, including the American Society for Bone and Mineral Research, the National Osteoporosis Foundation, the International Society for Clinical Densitometry, and the International Osteoporosis Foundation.It calculates the 10-YEAR PROBABILITY OF OSTEOPOROTIC FRACTURE using WHO's fracture Assessment calculator with age, sex, weight, height, clinical risk factors, and femoral neck BMD. | 6 Months | |
Secondary | TIMED UP AND GO TEST | According to Shumway Cook et al., the TUG is a sensitive and specific measure of probability for older adults' falls.The Test is considered a simple and validated method used clinically to assess the patients' functional mobility. During the administration of the Test, the patient is desired to stand up from a chair. Walk for three meters, turn back, walk back and then sit down back on the chair. | 6 Months | |
Secondary | FUNCTIONAL REACH TEST | The Functional Reach Test is a clinical evaluation tool for dynamical balance in one easy task. In standing, the length of an outstretched arm is measured to the maximum forward extent while maintaining a fixed support base (Physiotherapy Rehabilitation of Osteoporotic Vertebral Fracture) | 6 Months | |
Secondary | MODIFIED SIT AND REACH TEST | The sit and reach test is a standard indicator of the lower back and hamstring muscles' flexibility. The standard sit-and-reach box is the test management tool. Wells and Dillon (1952) described this Test for the First Time and is now widely used as a general flexibility test. | 6 Months | |
Secondary | FIVE TIMES SIT-TO-STAND TEST | A sit-to-stand (STS) movement is considered a fundamental prerequisite for mobility and functional independence. The FTSST measures the Time taken to stand five times from a sitting position as quickly as possible. Researchers have described its use as a measure of lower limb strength, balance control, fall risk and exercise capacity. | 6 Months | |
Secondary | BORG REVISED CATEGORY-RATIO SCALE (0 TO 10 SCALE) | The scale allows individuals to subjectively rate their exertion level during exercise or exercise testing (American College of Sports Medicine, 2010). It is based on the category-ratio (0-10) RPE scale (BORG-CR10) developed by Borg. The RPE scale is used to measure the intensity of exercise. The RPE scale runs from 0 - 10. The numbers relate to phrases used to rate how easy or strenuous activity. | 6 Months | |
Secondary | DYSPNEA INDEX | A clinical measure of shortness of breath for determining exertion levels. The Baseline Dyspnea Index (BDI) measures the severity of dyspnea at the baseline (or the beginning of a clinical trial). The Transition Dyspnea Index (TDI) measures changes from this baseline (transition period) at subsequent visits.
Levels of shortness of breath (SOB) 0=No SOB; can count to 15 (takes about 8 seconds) without taking a breath in the sequence. Mild SOB; can count to 15 but must take one short breath in the sequence. Moderate SOBneed to take 2 breaths to count to 15 in the sequence. Definite SOB; must take 3 breaths in the sequence of counting to 15. Severe SOB; unable to count or speak |
6 Months | |
Secondary | DIGITAL HAND-HELD DYNAMOMETER | Hand dynamometer has excellent reliability to test grip strength. It is reported as an indicator of total body strength, an objective test for physical capability, and a valid predictor of work capacity, degree of disease/injury, and rehabilitation outcomes. | 6 Months | |
Secondary | QUALITY OF LIFE EVALUATION: ECOS-16 QUESTIONNAIRE | ECOS-16 was developed to evaluate Quality of life in postmenopausal osteoporotic patients based on the osteoporosis specific quality of life instruments QUALEFF and OQLQ. (62)ECOS-16 contains 12 items from QUALEFFO and four items from OQLQ. The 16 items in ECOS-16 are divided into physical functioning, pain, fear of illness and psychosocial function. Five response options are offered per item with scores varying between 1 and 5 points, where 5 represents the worst QoL score. In this study, ECOS-16 will be translated first in the Urdu language, and then after its validation check, it will be used to measure Quality of life in study participants. | 6 Months |
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