Effect of Different Weight Vests on Body Weight in Obese Individuals

STUDY OBJECTIVES AND ENDPOINTS Primary objective To determine if wearing a weight vest with 11 % of an individual's body weight for 3 weeks decreases body weight in obese study subjects. Secondary objective To determine if wearing a weight vest with 11 % of an individual's body weight for 3 weeks affects fat mass, bone mass, muscle mass, water mass, fat free mass, physical activity and food intake in obese study subjects. To determine if wearing a weight vest with 11 % of an individual's body weight for 3 weeks affects plasma concentrations of glucose, insulin, HDL, LDL, TAG, FGF21, osteocalcin, FGF23, FGF15, sclerostin, lipocalin-2, leptin, ghrelin, GLP-1, GLP-2, CCK, (3-36)PYY, glucagon, renin, methoxynorepinephrine, Na, K, Cl, Ca and creatinine. STUDY DESIGN AND PROCEDURES Overall study design and procedure protocol The aim of the study is to investigate the effect of adding synthetic weights to obese individuals. The weights will be added as a weight vest with 11 % of the individual's body weight and will be worn for three weeks. Half of the study subjects will be given a weight vest with 11 % of body weight and half of the study subjects will be given a light weight vest. The light weight vest consists of a weight vest with most of the weights removed. The weight of the light vest will be 1 % of body weight giving a difference of 10 % between the groups. Body weight, fat mass, bone mass, water mass and fat free mass will be measured before and after the intervention by medical personnel to determine the effect of added synthetic weights on obese subject. This will be measured using bioelectrical impedance analysis (BIA) (MC-180MA, Tanita). The scales will be calibrated every week during the study to make certain reliable measurements. Pedometers will be used to measure the subject's activity each study day. We will also encourage the study participants to report food intake, choice of food and level of hunger each week. This will be done using the validated poll MiniMealQ(9). A pedometer will also be attached to the vests to check the daily use of the vests. The study persons will be informed about this arrangement. Fasting blood sampling will be performed before and after the intervention to further determine the effects of adding synthetic weights to obese individuals but also to elucidate the mechanism behind the "gravitostat". Blood glucose levels will be measured immediately. Blood samples, except blood glucose, will be analyzed either continuous or after all study subjects have been enrolled depending on human resources. Study subjects will be recruited by advertising in the local newspaper. Study subjects will be informed about hypothesis that people carrying a heavy or light weight may differ in weight loss. At this point it is not known if the heavy weight vest or the light vest is causing more weight loss, as no one has performed similar studies on humans. Study subjects will have one week to familiarize themselves with the equipment used in the study before the intervention starts. This is to minimize human errors during the intervention and ensure a high level of compliance. The data collected during this week will be used as baseline. Day 1 - enrollment The first 100 persons to contact the researchers will be enrolled in the study. In order to be enrolled a study subject also need to meet all the inclusion criteria and not meet any of the exclusion criteria. The study subjects will be entitled to a private meeting with one of the researchers. Study subjects will receive information about the study plan both orally and written during this meeting. Consumption of more than one liter of wine (11 %) or alcohol equivalent during a study week will not be accepted. Drastic change in lifestyle before or during the study will not be accepted. Any study subject failing to comply with this restriction will instantly be removed from the study. Education and detailed planning of the study subjects will be performed after written consent is obtained from the study subject. Body weight, fat mass, bone mass, water mass and fat free mass will be measured using BIA. It is unlikely that bone mass and water mass will be affected during the short time of this study but these values are easily obtained during the measurements. We will also measure blood pressure, height in order to calculate BMI and collect each subject's age and gender. This meeting will end with a blood sample to screen for common diseases that may distort the results and increase the risk of adverse effects. We will measure the following substances in blood: hemoglobin, white blood cells, trombocytes, sodium, potassium, creatinine, ASAT, ALAT, HbA1c, C-reactive protein (CRP), T4, TSH. Also, we will use urine dipsticks to further screen for diseases. We will measure the following substances in urine: nitrite, white blood cells, red blood cells, glucose, creatinine and albumin. Only subjects were all above substances are within normal levels will be included in the study. Study subject will be able to contact the researchers by e-mail or mobile phone any time during the study if questions arise. Day 8 - intervention starts Study subjects will be entitled to another appointment with the researchers and the nurse from Gothia Forum one week after the enrollment. Body weight, fat mass, bone mass, fat free mass and water mass will be measured during this meeting using BIA. Fasting blood sampling by an experienced nurse from Gothia Forum will be performed when the researcher believe that the study subject is fully educated and ready to be enrolled in the study. A maximum of 25 ml will be collected at each blood sampling. Plasma levels of glucose will be measured instantly in capillary blood, and thus not be dependent on successful venous blood sampling. Venous blood samples for other measurement than glucose will be centrifuged by the researchers or personnel from Gothia Forum to obtain serum or EDTA plasma samples. Serum and plasma samples may be stored at a temperature of -80°C until analysis. Study subjects can request to have their blood samples destroyed at any time. The intervention will start directly after blood sampling. Subjects will earn a randomized three character code to be used throughout the study; this will be noted in a digital only randomization list. Study subjects will obtain either a weight vest with 11 % of body weight or a light vest weighing 1 % of body weight. The vest is to be worn 8 hours each day for the following 3 weeks. The vest is only to be used during awake hours. Day 15 Study subjects will be entitled to another appointment with the researchers two weeks after the enrollment, this appointment may be performed by telephone if the subject so agree. Any problems with compliance will be discussed. Study subjects who deviate more than 20 % from the study protocol will be removed from the study. Study subjects will continue to wear the vests for 8 hours each day. Day 22 Study subjects will be entitled to another appointment with the researchers three weeks after the enrollment, this appointment may be performed by telephone if the subject so agree. Any problems with compliance will be discussed. Study subjects who deviate more than 20 % from the study protocol will be removed from the study. Study subjects will continue to wear the vests for 8 hours each day. Day 29 - intervention ends Study subjects will be entitled to another appointment in the morning before breakfast with the researchers and the nurse from Gothia Forum four weeks after the enrollment. Body weight, fat mass, bone mass, fat free mass and water mass will be measured during this meeting using BIA. Fasting glucose will be measured in capillary blood. Venous blood sampling will be done. Study subjects will have worn the vests for 8 hours the day before, but they will not wear it during the visit the morning of day 29. The appointment at day 29 may also be performed on "day 30" depending on the study subject's schedule. Nevertheless, last day for the intervention is on study day 29. Rationale for study design In order to avoid the risk of carry-over effects, we have decided to not use a crossover design. This could have decreased the variation of the measurement values and increased the power of the study. However, we believe there could be a risk of a carry-over effect with a cross over design. As this is a completely new effect in clinical studies, we have no information about the wash-out time needed to avoid this problem.