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hero etiketine sahip kayıtlar gösteriliyor. Tüm kayıtları göster

17 Kasım 2016 Perşembe

Sea Hero Quest is of huge benefit to medical researchers. So what’s the catch? | Emily Reynolds

In tech circles, alongside words such as “scaleable” and “the gig economy”, you often hear the phrase “tech for good” bandied around. Sometimes it’s a fairly innocuous but ultimately toothless concept, essentially denoting the idea that technology has the potential to be a driver for positive social change but not doing very much about it. Other times it can take on a more creepily utopian tone, suggesting that should the world more closely represent the shiny libertarian enclaves of Silicon Valley, the world’s problems would be solved. And sometimes – just sometimes – it does what it says on the tin.


A new game, designed to test spatial navigation, appears at first glance to do just that. Sea Hero Quest, which involves navigating a boat through choppy waters, contains a diagnostic test for the early signs of Alzheimer’s disease. The game has now been played by more than 2.4 million people – which the team behind the game say makes it the largest dementia study in history.


It’s now set to be adapted for use in a clinical setting – data could be fed back to clinicians, allowing for earlier diagnosis, better understanding of how medication is working for a particular patient and a more accurate and precise measurement of a patient’s decline. It could even be incorporated into NHS programmes.


This, it goes without saying, is initially incredibly attractive. Understanding and managing an illness or being alerted when you’re at risk simply through the daily use of an app sounds simple, easy and most of all useful. Could this not be a genuine use of tech for good, rather than the banal and empty proclamations often heard from CEOs and founders?


In theory, yes. In practice: maybe not.



More than 2.4 million people have downloaded Sea Hero Quest to their phones.


More than 2.4 million people have downloaded Sea Hero Quest to their phones. Photograph: The Sea Hero Quest/PA

As with any health data-driven project, it comes with stipulations. A recent study in Lancet Psychiatry suggested that data gathered on Facebook could provide a “wealth of information” about mental health, with a series of language analysis and facial emotion recognition algorithms providing “insights into offline behaviours”. This, too, sounds great. Having your health monitored and managed through the passive use of technology you probably already use – what more could you want?


But there are a number of concerns here: primarily, the safety of private health data. The addition of a private company in the latter study may make it feel different: a towering behemoth such as Facebook obviously feels more threatening than something set up for and run by clinicians. But to not have the same reservations just because the data was being sent to scientists would be incredibly naive.


Science, much like technology, is often presented as objective, reasonable fact, without mentioning the very obvious caveat that it is conducted by human beings, who are often neither reasonable nor objective. Multiple studies about statistical analysis are useful to recall here – the results of such analyses may seem completely objective, but often reflect the preconceived biases of those conducting them. That’s not to say that would be the case with Sea Hero Quest, of course: just that the results of such research can be fallible.


And it’s also important to remember that, should the Conservative party have its way, the NHS may be in the hands of several, separately operated and privately owned companies before too long. This adds further complications: who would have access to our health data? How would they use it? How would data be efficiently and safely communicated across different companies? Would their data protection processes be cohesive? Would they be meticulous enough to protect our most private, personal data? The idea of having your phone feed data to a central NHS database sounds great in principle, but these questions would need to be answered before that could safely become a reality.


In an ideal world, tech would be utilised to help us to diagnose and treat illnesses: anything that can efficiently and effectively help people manage long-term or life-threatening conditions can only be a good thing. Similarly, the idea of a National Health Service that is genuinely innovative, that uses new ways to help people and that has a strong grasp on data security while it does so is incredibly appealing. Unfortunately, as with most utopian ideas, you’re left wondering whether it might just be too good to be true.



Sea Hero Quest is of huge benefit to medical researchers. So what’s the catch? | Emily Reynolds

16 Kasım 2016 Çarşamba

Sea Hero Quest: the mobile phone game helping fight dementia

A mobile phone game that tests spatial navigation skills and has been played by 2.4 million people, has become the largest dementia study in history and raised hopes of a breakthrough in diagnosing the disease.


Sea Hero Quest, a collaboration between Alzheimer’s Research UK, Deutsche Telekom, game designers Glitchers and scientists, has generated the equivalent of 9,400 years of lab-based research since its launch in May.


Experts hope to use the data to create the world’s first global benchmark for spatial navigation, one of the first abilities affected by dementia, and to develop the game into an early diagnostic test for the disease, which is the leading cause of death in England and Wales.


Dr Hugo Spiers, of University College London, who presented the preliminary findings at the Neuroscience 2016 conference in San Diego, said: “This is the only study of its kind, on this scale, to date. Its accuracy greatly exceeds that of all previous research in this area. The findings the game is yielding have enormous potential to support vital developments in dementia research. The ability to diagnose dementia at early stages, well before patients exhibit any signs of general memory loss, would be a milestone.


“This study is thus now giving us the opportunity to make a real difference to the lives of millions of people living with dementia and those at risk of developing the disease in the future.”


Sea Hero Quest requires players to navigate a boat through waters in differently themed areas over 75 levels, collecting items along the way. It was designed to appeal to all gamers, rather than just people wanting to contribute to a good cause, and its popularity has seen the number of players soar past the original target of 100,000 by the end of the year.


Players provide their age and sex, allowing the scientists to chart their performance against other users.


Spiers said they could now create the equivalent of a height chart whereby if someone was particularly short – or in this case if their spatial navigation ability was particularly low – for their age and sex it would raise a red flag.


By testing a person’s spatial navigation abilities, the game could allow for diagnosis and treatment of patients far earlier.


Spiers said Sea Hero Quest, which will now be adapted for use in a clinical setting, could also be used to track decline and in drug trials to test the impact of the medication.


Alzheimer’s Research UK’s chief executive, Hilary Evans, praised the role of Deutsche Telekom, which has spent more than €1m (£860,000)on the project, including marketing.


“The early data that has very quickly been generated by Sea Hero Quest should inspire other corporations to consider what assets they might bring to research into dementia or any of our most seemingly intractable medical conditions,” she said.


The experts found differences in spatial navigation strategies employed by men and women, and also that spatial navigation abilities began to decline from early adulthood. For example, players aged 19 (the youngest in the study) had a 74% chance of accurately hitting a target during the game, compared with 46% among 75-year-olds (the oldest in the study). This decline over time contradicted previous studies – typically based on less than 100 people – which suggested cognitive abilities do not decline until later in life.


They also found that players in Nordic countries showed notable spatial navigation capabilities.


The scientists will carry out further analysis of the data over the next two years. In the meantime, the game continues to be available for free download and the data generated will contribute to the ongoing research.



Sea Hero Quest: the mobile phone game helping fight dementia

15 Mart 2014 Cumartesi

Salute by England hero says we"re battling for Jack"s life

“The much more publicity we get, the much more opportunity there is of locating a remedy for Jack,” explained Mr Johnson, 39. “Owen was giving a display of power.”


The salute has been carried out by everybody from Bradley Wiggins – an additional Wigan lad – to Rio Ferdinand, Tim Henman, and even Ant and Dec.


But the Johnsons are a rugby loved ones. Mr Johnson was a professional player, and played alongside Owen Farrell’s father.


So when the England fly-half carried out the gesture it was special, particularly at such a large-profile second.


The locked fingers represent the initials of Joining Jack, the charity set up by the Johnsons to fund investigation into Jack’s sickness, Duchenne muscular dystrophy (DMD).


This condition, which is degenerative and terminal, affects one in 350,000 boys. In unusual cases, it can also have an effect on girls.


Jack – a slight, affectionate boy with green eyes, a passion for Lego, and a mischievous smile – was diagnosed with the condition in October 2011.


The muscle groups in his legs have previously started out to waste away. He cannot maintain up with his buddies at college, and is not allowed to use stairs for worry of damaging his fragile legs.


By the time he is eight, Jack will call for leg braces to walk. When he is twelve, he will be confined to a wheelchair. After that, the muscle tissue in the rest of his physique will also start off to degenerate, such as his heart and lungs.


At some point he will grow to be completely paralysed, and will depend on a ventilator to breathe. Sufferers rarely live beyond the age of 30. There is no recognized cure.


For Mr and Mrs Johnson, considering about the long term is extremely hard. Alternatively, they focus on the difficulties right here and now.


“Jack loves rugby, but it upsets you when all the lads run off and he is left behind,” stated Mrs Johnson, 29. “He doesn’t like to speak about things or truly feel various, but he tends to ask me queries when I’m driving him to school. He’ll ask why he cannot join in the game, or why he can not run as quick as the other boys.


“I tell him that his muscle tissue are poorly, but I try out and reinforce the reality that he’s great at other issues like Lego and drawing. But it breaks your heart.”


As if on cue, Jack pads into the space in his Superman socks, in search of Lego figures. Mr Johnson will get up to support him, and his wife goes to find him a clean shirt it is clear from this each day affection that the couple are making every single hard work to give their son a standard daily life.


“There are several new drugs in advancement that look really fascinating as achievable game changers,” explained Mr Johnson, once his son is taking part in in the subsequent room, securely out of earshot. “It’s torture to think that the cure could be out there. Joining Jack is funding 4 new drug research, and we are hoping to fund two more.


“The one day we dread is when we have to tell Jack the seriousness of his condition. I truly hope that never happens. It’s a race against the clock for us and a whole generation of other sufferers.”


At the minute, Jack is on potent steroids, which assist to slow his muscle degeneration. Over time, however, side effects will start to manifest, including osteoporosis, cataracts, excess weight-obtain, facial swelling, hair growth and bursts of anger. This creates extra stress to strive for a long term cure.


When Jack was first diagnosed, his father recalls “staring at a wall for 45 minutes”, unable to uncover a way to react.


Over the following 12 months, he was “up all evening on my telephone, studying all about the ailment, paper right after paper after paper”. Even right now, 3 years on, Mr Johnson is typically unable to focus at work – he owns a signage organization – and ends up “walking close to the office in a daze”.


Mrs Johnson, who has provided up perform to volunteer for the charity full-time, usually feels “panicked”, fearful and worn out. Both discover themselves in tears almost every single day. But for Jack’s sake, they can not give up.


Rugby is at the heart of the Johnsons’ daily life, and Wigan is a massive rugby town. Mr Johnson was a expert player for 12 many years, seven of which had been invested playing for Wigan Warriors, the neighborhood Rugby League staff. He has acknowledged Owen Farrell all his existence.


“I remember Owen as a 3-12 months-old, coming into the shifting area with a rugby ball,” he recalled. “He utilised to trip his bike previous our window on his way house from college, and I went to school with his mum, Coleen. She has turn into a genuine shoulder for Alex to cry on.”


From the really beginning, the England fly-half was deeply moved by Jack’s plight.


“[I carry out the salute] because it’s a lead to shut to my heart,” Farrell informed the Sunday Telegraph. “If the result in touches you sufficient, it gets to be portion of your considering instinctively, specifically when you can attain out to such a massive audience.


“When you recognize the lack of awareness of this kind of a situation, every person has to leap on board and do their bit.”


The Johnsons’ struggle has galvanised the rugby neighborhood into action. Wigan players at all amounts frequently complete the Joining Jack salute at games. Income has been raised by sponsored runs, skydives and cake sales, and the couple have a sound network of help. A 10km charity run that they organised in September was attended by 2,600 folks, and they are hoping for an even better turnout this 12 months.


This week, in a important improvement, a campaign supported by Joining Jack has borne fruit. On Friday, the Department of Wellness announced a new scheme to rapidly-track breakthrough medication to seriously unwell patients, cutting the length of time amongst clinical trials and widespread use to just five many years (it generally will take amongst ten and 15 many years).


Duchenne muscular dystrophy will be 1 of the very first situations to advantage from rapidly-tracked medicines.


With this obstacle lifted, the couple are redoubling their efforts to discover possibly lifesaving new medicine.


“We get a rugby-variety mindset,” stated Mr Johnson. “We set out to do a task, determine the obstacles and just get on with it. We’re striving to tackle the condition out the way, and give the charity the greatest push ever. If we can make strides more than the next couple of years, Jack’s generation of sufferers will have a hope of a normal lifestyle.”


“The prize is a enormous one,” added his wife. “But if we don’t get there, and we shed Jack, I can not envision how that would be.”


The most difficult part is realizing that day by day, Jack’s time is obtaining shorter. But, as Mrs Johnson puts it, both parents are “giving almost everything we have to this fight of all fights.”


And they have every thing to perform for.


To donate to the Joining Jack fund, check out joiningjack.org



Salute by England hero says we"re battling for Jack"s life

17 Ocak 2014 Cuma

Wife of WW2 hero pilot "made to wait for care soon after stroke"

She wrote: “When my mom suffered inadequate care following a 2nd stroke at this care home, Adeline had the courage to safeguard her against a program that is not unknown for closing ranks.


“As a end result my mom was hospitalised and has virtually miraculously recovered.


“Hearing how typically carers see and even report unwell-treatment or neglect in care homes, but nevertheless get ignored or are intimidated into silence, is scary.


“Those with households or friends to look out for and communicate for them are the fortunate ones. But what of those without having? Who will be their voice?”


Ms Dalley, 34, was horrified when she was advised to depart Lady Bader “to see a GP on Monday” after she suffered the stroke.


She advised the Everyday Mail: “Poor Lady Bader is in her fourth residence due to poor care.


“Wendy’s foreword talks a great deal about how Sir Douglas would have accepted of my book. I looked after Joan following she suffered a stroke but I was not permitted to act.


“So I went even more to safeguard everybody at the house – even though no one else would speak up. So several carers are intimidated into silence.”


Lady Bader’s late husband, Sir Douglas, misplaced the two his legs in a crash, and is regarded as 1 of Britain’s best war heroes.


Bader, who misplaced his legs in a crash before the 2nd Globe War, was capable to use his disability to his advantage in tight turns.


Even though the g-force would cause capable-bodied pilots to blackout as blood rushed from their heads to their legs, Bader, who had each legs amputated following a crash in 1931, could recover far more quickly.


Bader had to bail out over France in August 1941 and invested the rest of the war as a prisoner of war. His story was informed in the movie Reach for the Sky, starring Kenneth More. He died in 1982.



Wife of WW2 hero pilot "made to wait for care soon after stroke"