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New Balance 619 v1 Men's Suede ... Cross-Training Shoes
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Ready to go? Get to the heart of Indonesia with one of Lonely Planet's in-depth, award-winning guidebooks.

Bali Full-Day Traditional Village Sightseeing Trip with Lunch

After pickup from your hotel, begin with a visit to a Batubulan village to see the center of handmade batik weaving. Afterward, head to Celuk Village to see the gold and silver smith, and to Mas, to learn about wood sculpture.Continue to Batuan Ubud, a village known for its artwork and distinct painting style that originated in the 1930s. Then travel to the Batuan Trinity Temple to see its intricate carvings and architecture up close. From there, make your way to Gunung Kawi Temple Sebatu, home to a holy water fount and large koi pond.Break for lunch at Kintamani, with views of Mt. Batur and its caldera lake. After lunch, head to the village of Tegalalang to taste Bali Luwak coffee and ginger tea, and see the spice garden and rice terrace. After some afternoon tea, visit the Ubud Village, a nature reserve and Hindu temple complex, as well as the Ubud Market and Ubud Palace then ending the trip by visiting Tegunungan Waterfall. Your day trip will conclude with transportation back to your hotel.

Denpasar Arrival Transfer: Airport to Hotel

Travel from Denpasar Airport to Kuta, Sanur, Nusa Dua, Legian and Seminyak. Transfer services are available 24 hours a day, 7 days a week. This is a shared vehicle transfer. When making a booking, you will need to advise your flight details and your accommodation details. Your transfer will be confirmed immediately and you will be provided with a travel voucher to present to the driver.Don't forget to book your Hotel to Airport transfer!

Bali Tour: Mt Batur, Sacred Monkey Forest, Spa Treatment

Volcano: Enjoy the fresh weather and beautiful landscape. Mt. Batur status is still active,the first documented eruption in 1804 and the last eruption with huge lava in 1974. Ubud City: This place is so famous and popular for tourist, this district has an open view of the rice terrace, forest, paintings, sculptures, wood carvings, silver smith and culture Monkey Forest: This area is a monkey habitat and protected by local government. The sacred monkey forest is not only for tourist attraction but good for economic life of local people and for research conservation programs. The visitor can enjoy and take pictures with monkeys and the surrounding atmosphere. Rice Terrace Field: Subak is an irrigation system for water management which was developed around 9th century. Subak system works without a machine pump. The water is taken from the above mountain and flows downward to irrigate rice fields and also used for construction. Temple: This public temple one of the places for praying for Hinduism.Majority religion citizen live in Bali is Hindu (Tirta Empul Temple) Luwak Animal: Luwak animal is a famous animal and contribute significantly to the production to coffee. Spa Treatment: After finished Tour relax with Spa Treatment for 2 hours. You can enjoy type of massage like Traditional Balinese massage and Javanese body scrub.

Bali Kintamani Volcano, Ubud and Barong Dance Full-Day Tour

Continue on through the woodcarving village of Mas. Watch artisans chipping intricate designs from wood blocks. Then visit the fantastic 11th century Elephant Cave (Goa Gajah) before moving into the cool mountains of Kintamani. View Mount Batur an active volcano with its ribbons of black lava running down its peak to the valley below. Beside lies the shimmering lake of Batur. Enjoy lunch in a restaurant providing wonderful views (lunch is at own expense). On the return back you will stop at the Holy springs which are believed to have magic curative powers. Visit Ubud the artistic heart of Bali and Celuk the gold and silver making center on route.

Denpasar Departure Transfer: Hotel to Airport

Travel from Kuta, Sanur or Nusa Dua, Legian and Seminyak to Denpasar Airport. Transfer services are available 24 hours a day, 7 days a week. This is a shared vehicle transfer. When making a booking, you will need to advise your flight details and your accommodation details. Your transfer will be confirmed immediately and you will be provided with a travel voucher to present to the driver.Don't forget to book your Airport to Hotel transfer!

Half-Day Electric Bike Tour of Ubud

Get ready for an awesome time! Start your tour with a pickup from your hotel in Ubud and be at the starting point in 15 minutes. That's right, our bikes are electric so no long, crowded van ride up the mountain just to roll down.Our spectacular tour goes from Ubud up to the famously stunning Tegalalang Rice Terraces. Tegalalang is a UNESCO world heritage site and once you arrive you will see why. Stop to take in the view. Allow the peaceful atmosphere to wash away your worries. After this, you’ll travel back to Ubud, riding through villages along the gorgeous back roads. Our guides are from Ubud and know all about the area. Theywill take you to beautiful temples and share their knowledge and experience with you.After returning to the starting point you will enjoy a delicious Balinese lunch. What a day!

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Indonesia photo credits

Design 10421 Kenneth Cole New York N4DCjKete

Glossary

Study record managers: refer to the Data Element Definitions if submitting registration or results information.

A type of eligibility criteria that indicates whether people who do not have the condition/disease being studied can participate in that clinical study.
An arm type in which a group of participants receives an intervention/treatment considered to be effective (or active) by health care providers.
An unfavorable change in the health of a participant, including abnormal laboratory findings, that happens during a clinical study or within a certain amount of time after the study has ended. This change may or may not be caused by the intervention/treatment being studied.
A type of eligibility criteria that indicates the age a person must be to participate in a clinical study. This may be indicated by a specific age or the following age groups:

The age groups are:

A method used to assign participants to an arm of a clinical study. The types of allocation are randomized allocation and nonrandomized.
A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment , or no intervention, according to the trial's protocol .
A general description of the clinical trial arm. It identifies the role of the intervention that participants receive. Types of arms include experimental arm , active comparator arm , placebo comparator arm , sham comparator arm , and no intervention arm .
Data collected at the beginning of a clinical study for all participants and for each arm or comparison group. These data include demographics, such as age, sex/gender, race and ethnicity, and study-specific measures (for example, systolic blood pressure, prior antidepressant treatment).
Indicates that the study sponsor or investigator recalled a submission of study results before quality control (QC) review took place. If the submission was canceled on or after May 8, 2018, the date is shown. After submission of study results, a study record cannot be modified until QC review is completed, unless the submission is canceled.
Information required by the Food and Drug Administration Amendments Act of 2007 . In general, this is a description of any agreement between the sponsor of a clinical study and the principal investigator (PI) that does not allow the PI to discuss the results of the study or publish the study results in a scientific or academic journal after the study is completed.
A sponsor or investigator may submit a certification to delay submission of results information if they are applying for FDA approval of a new drug or device, or new use of an already approved drug or device. A sponsor or investigator who submits a certification can delay results submission up to 2 years after the certification/extension first submitted date, unless certain events occur sooner. See Delay Results Type in the Results Data Element definitions for more information about this certification.
The date on which information about a certification to delay submission of results or an extension request was first available on ClinicalTrials.gov. ClinicalTrials.gov does not indicate whether the submission was a certification or extension request. There is typically a delay between the date the study sponsor or investigator submitted the certification or extension request and the first posted date .
The date on which the study sponsor or investigator first submitted a certification or an extension request to delay submission of results. A sponsor or investigator who submits a certification can delay results submission up to 2 years after this date, unless certain events occur sooner. There is typically a delay between the date the certification or extension request was submitted and the date the information is first available on ClinicalTrials.gov ( certification/extension first posted ).
The date on which the study sponsor or investigator first submitted a certification or an extension request that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a certification or extension request one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria. Meeting QC criteria for an extension request does not mean that the National Institutes of Health (NIH) has determined that the request demonstrates good cause. The process for review and granting of extension requests by the NIH is being developed.
In the search feature, the City field is used to find clinical studies with locations in a specific city. The Distance field is used to find studies with locations within the specified distance from a city in number of miles. For example, if you choose Illinois as the state , identifying "Chicago" as the city and "100 miles" as the distance will find all studies listing a location within 100 miles of Chicago.
A research study involving human volunteers (also called participants) that is intended to add to medical knowledge. There are two types of clinical studies: interventional studies (also called clinical trials) and observational studies .
Another name for an interventional study .
The unique identification code given to each clinical study upon registration at ClinicalTrials.gov. The format is "NCT" followed by an 8-digit number (for example, NCT00000419).
An organization other than the sponsor that provides support for a clinical study. This support may include activities related to funding, design, implementation, data analysis, or reporting.
The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.
The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.
In the search feature, the Country field is used to find clinical studies with locations in a specific country. For example, if you choose the United States, you can then narrow your search by selecting a state and identifying a city and distance .
A type of intervention model describing a clinical trial in which groups of participants receive two or more interventions in a specific order. For example, two-by-two cross-over assignment involves two groups of participants. One group receives drug A during the initial phase of the trial, followed by drug B during a later phase. The other group receives drug B during the initial phase, followed by drug A. So during the trial, participants "cross over" to the other drug. All participants receive drug A and drug B at some point during the trial but in a different order, depending on the group to which they are assigned.
A group of independent scientists who monitor the safety and scientific integrity of a clinical trial . The DMC can recommend to the sponsor that the trial be stopped if it is not effective, is harming participants, or is unlikely to serve its scientific purpose. Members are chosen based on the scientific skills and knowledge needed to monitor the particular trial. Also called a data safety and monitoring board, or DSMB.
A phase of research used to describe exploratory trials conducted before traditional phase 1 trials to investigate how or whether a drug affects the body. They involve very limited human exposure to the drug and have no therapeutic or diagnostic goals (for example, screening studies, microdose studies).
The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers , has age or age group requirements, or is limited by sex .
The number of participants in a clinical study. The "estimated" enrollment is the target number of participants that the researchers need for the study.
A type of eligibility criteria . These are reasons that a person is not allowed to participate in a clinical study.
A way for patients with serious diseases or conditions who cannot participate in a clinical trial to gain access to a medical product that has not been approved by the U.S. Food and Drug Administration (FDA) . Also called compassionate use. There are different expanded access types .

For more information, see FDA Expanded Access: Information for Patients .

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