Healthy Behaviors Learning Task and Sleep (NAP)
Sleep Conditioning and Healthy Food Choices
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Over 1/3 of U.S. adults over the age of 20 are obese and obesity is associated with a host of deleterious medical comorbidities, including heart disease, type 2 diabetes, and cancer, costing the U.S. approximately $147 billion annually. Novel approaches to address this public health crisis are needed. Although obesity is multiply determined, it is ultimately a disorder of positive energy balance, such that weight loss requires increases in physical activity and improvements in choosing healthy over unhealthy foods. People who are strongly motivated to eat are more obese, and derive less benefit from weight loss treatments. There are two general approaches to addressing this pattern: 1) increase the reinforcing value of healthy foods and/or 2) increase an individual's self-control, i.e., the ability to inhibit approach responses to less healthy foods.
Emerging research has begun to develop and test training programs that directly modify tendencies to approach one type of stimulus while resisting temptation of another type of stimulus for problems other than obesity. For example, researchers have been able to train heavy drinkers to decrease their weekly alcohol intake7 and chocolate-lovers to reduce their chocolate intake. However, these researchers did not also incorporate increasing interest in alternatives (e.g., drinking water instead of beer). This training mechanism has also yet to be applied to research on obesity and decreasing intake of unhealthy foods.
Participants will be first trained via a computerized training task to inhibit responses to high-calorie (unhealthy) foods, and to approach alternative low-calorie, high-nutrient (healthy) foods, in order to test the tasks efficacy. The investigators will include the training task and incorporate a nap component consistent with Hu and colleagues to evaluate the utility of sleep conditioning for maintaining training-related changes in inhibition and approach tendencies after one week. Tones played during the training task will be played again during the nap, based on randomization
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
Maryland
-
Baltimore, Maryland, Estados Unidos, 21224
- Johns Hopkins University Bayview Campus, Behavioral Medicine Research Lab
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Age between 20 and 55, inclusive
- Body mass index ≥ 25
- Nonsmoker and non-nicotine user for a minimum of the past 6 months
- Not currently using recreational drugs
- Desire to lose weight
- Difficulty losing weight in the past
- AUDIT: <3 women, <4 men (note: score of 4 is okay if both items 2 and 3=0)
- Pittsburgh Sleep Quality Index questionnaire score <8
- Insomnia Severity Index questionnaire score <10
- Epworth Sleepiness Scale <10
- Below the clinical cutoff for Restless Leg Syndrome
- Full sleep cycle between 8:00pm and 9:00am at least 6 days per week
- Apnea hypopnea index <15, as measured by the Nox-T3
Exclusion Criteria:
- Current diagnosis of diabetes mellitus (type 1 or type 2)
- History of major medical disease impacting study
- Significant unstable medical morbidity within the past 6 months
- Significant unstable psychiatric disorder within the past 6 months
- Current use of antidepressants or opioids.
- Lifetime diagnosis of anorexia nervosa or bulimia nervosa
- Lifetime alcohol or substance abuse disorder or dependence
- Suicidal ideation in past year
- Lifetime serious head injury or stroke judged to impact pain or sleep
- Sleep disorder as assessed via the Structured Interview for sleep disorders (SIS-D).
- Women who are pregnant or lactating.
- Unwilling to follow study procedures
- Other (reason judged by PI)
- Food allergies: Individuals who report any food allergies or any history of anaphylactic reactions related to study procedures during the phone screen for this study will be excluded from participation. Participants who report avoidance of specific foods for other medical reasons (e.g., an interaction between a prescribed medication and a food group, food triggered migraines), if they are related to study procedures, will also be excluded from participation.
- Takes participant more than 30 minutes to fall asleep
- Positive toxicology screen
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Triplo
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Approach/Inhibit group
Participants in the experimental group and control sham sound cues group will complete the Modified Go/No-Go Task. Following completion of post-training assessment measures, participants will be given the opportunity to take a 90-minute while undergoing real-time sleep monitoring. White noise will be played via headphones. Upon entering Stage N3 sleep and/or after having been asleep for 20 minutes and currently in any stage sleep other than N1, sound cues will be played to participants via headphones based on their randomization to 1 of 3 experimental groups. |
Participants in the experimental group and control sham sound cues group will complete a computerized training task to facilitate learning to respond (press a computer key) to healthy food stimuli and to inhibit responses (not press a computer key) to unhealthy food stimuli.
Participants in the control sham go/no-go group will complete a similar task with common office supplies (approach) and tools (inhibit).
All participants will also complete a 24 hour dietary recall as described below.
|
|
Comparador Falso: Sham sound cues group
Participants in the experimental group and control sham sound cues group will complete the Modified Go/No-Go Task. Following completion of post-training assessment measures, participants will be given the opportunity to take a 90-minute while undergoing real-time sleep monitoring. White noise will be played via headphones. Upon entering Stage N3 sleep and/or after having been asleep for 20 minutes and currently in any stage sleep other than N1, sound cues will be played to participants via headphones based on their randomization to 1 of 3 experimental groups. |
Participants in the experimental group and control sham sound cues group will complete a computerized training task to facilitate learning to respond (press a computer key) to healthy food stimuli and to inhibit responses (not press a computer key) to unhealthy food stimuli.
Participants in the control sham go/no-go group will complete a similar task with common office supplies (approach) and tools (inhibit).
All participants will also complete a 24 hour dietary recall as described below.
|
|
Comparador Falso: Sham go/no-go group
Participants in the control sham go/no-go group will complete a modified Go/No-Go Task with sham approach and inhibit items. Following completion of post-training assessment measures, participants will be given the opportunity to take a 90-minute while undergoing real-time sleep monitoring. White noise will be played via headphones. Upon entering Stage N3 sleep and/or after having been asleep for 20 minutes and currently in any stage sleep other than N1, sound cues will be played to participants via headphones based on their randomization to 1 of 3 experimental groups. |
Participants in the experimental group and control sham sound cues group will complete a computerized training task to facilitate learning to respond (press a computer key) to healthy food stimuli and to inhibit responses (not press a computer key) to unhealthy food stimuli.
Participants in the control sham go/no-go group will complete a similar task with common office supplies (approach) and tools (inhibit).
All participants will also complete a 24 hour dietary recall as described below.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Reinforcing Value of Food assessed by the Reinforcing Value of Food Questionnaire
Prazo: Approximately 1 week (after second assessment has been taken)
|
The reinforcing value of food task (RVF) assesses how hard an individual is willing to hypothetically work to gain access to food compared with an alternative.
A series of paired-samples t-tests will be calculated in order to determine whether participants' scores on the reinforcing value of food test changed between baseline and 1 week later.
Scores on the RVF have been shown to be associated with BMI. as well as obesity and energy intake.
|
Approximately 1 week (after second assessment has been taken)
|
|
Delay of Gratification assessed by the Kirby Questionnaire
Prazo: Approximately 1 week (after second assessment has been taken)
|
A series of paired-samples t-tests will be calculated in order to determine whether participants' scores on the Kirby Questionnaire changed between baseline and 1 week later.
Each item is scored based on whether the participant chooses the shorter delay and less monetary reward versus the longer delay and a higher monetary reward.
Delay-discounting rates are positively correlated with impulsiveness.
|
Approximately 1 week (after second assessment has been taken)
|
|
24 hour dietary recall: Nutrition Data System for Research (NDSR) assessed by the Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24) dietary food recall
Prazo: Approximately 1 week (after second assessment has been taken)
|
We will use paired-samples t-tests to determine whether participants mean caloric intake and macronutrient breakdown (e.g., %calories from fat) from the two dietary recalls pre-training task were significantly different from their means post-training task.
|
Approximately 1 week (after second assessment has been taken)
|
|
Go/no-go task assessed by the Go/no-go task
Prazo: Approximately 1 week (after second assessment has been taken)
|
Performance on go/no-go task as measured by reaction time and accuracy (combined into one score) will be correlated with baseline measures of dietary characteristics and disinhibition
|
Approximately 1 week (after second assessment has been taken)
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Michael T Smith, Ph.D, Johns Hopkins University
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- IRB00101818
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .