Seasonal Patterns of Stress, Diet and Physical Activity - Life in All Seasons (LENAS)
NCT ID: NCT01674296
Last Updated: 2020-05-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
52 participants
OBSERVATIONAL
2012-06-30
2014-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This study will illuminate season's role in changes in energy balance related behaviors and body weight and composition. Ultimately, this information will be used to identify factors affecting food consumption and individual activity during seasonal periods to help to segment interventions for obesity prevention in mid-life women.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Lifestyle, Eating, and Activity Patterns
NCT00944099
Examining the Longitudinal Relationship Between Sleep and Weight Gain in College Students
NCT04100967
Assessing the Impact of Perceptions of Unpredictability on Objective Measures of Food Consumption and Metabolism
NCT06690294
Diet, Physical Activity, and Sleep Habits
NCT04035421
The Effect of Time-restricted Feeding on Physiological Function in Middle-aged and Older Adults
NCT02970188
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Specific aims:
1. To identify seasonal changes in %BF of mid-life women.
Participant's percentage of body fat will fluctuate, and will be highest at the end of the winter season and lowest at the end of the summer season.
2. To describe predictors of seasonal changes in %BF.
There will be no intervention other than frequent monitoring of food consumption, individual activity and individual- level factors thought to influence food consumption and activity such as dietary restraint, subjective stress, sleep quality and duration, and physiological stress as measured by allostatic load. The volunteers will be asked to complete a 7-day activity and energy expenditure monitoring period (along with body composition assessment, questionnaires regarding individual factors thought to affect food consumption and activity, blood draw and urine collection to measure allostatic load) in each of the four seasons over a 12-month period; between monitoring periods they will come to the GFHNRC for measurement of weight, skin carotenoids for assessment of fruit and vegetable intake, and to provide a morning urine sample monthly (8 times), and receive emails reminding them to log on to a secure server and complete a 24-hr recall 3 times a month (36 times during the year).
The ASA-24 will be administered to assess nutritional intake; Actigraph GT3X+, Actitrainer, and QStarz GPS logger will be used to assess physical activity. Physiological stress will be assessed using the allostatic load index.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group 1 (2012-2013)
Monitoring of Dietary Intake, Physical Activity and Stress
No interventions assigned to this group
Group 2 (2013-2014)
Monitoring of Dietary Intake, Physical Activity and Stress
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Weight stable (±10 lbs) for at least 6 months prior to the start of the study
* Body mass index (BMI) between 18-35 kg/m2
* Access to high-speed internet
* Willing to comply with study requirements
Exclusion Criteria
* Current smoker or tobacco or nicotine use
* Male sex
* Age \<40.0 or \>60 years
* Health conditions (cardiovascular, pulmonary, orthopedic, asthma) that would limit participation in physical activity
* Medications that would influence appetite, weight gain or weight loss.
* Intentional changes in diet or large increases in physical activity for the purpose of weight loss during the study. Typical weight maintenance behaviors are not an exclusion criterion.
* Pregnant, lactating, or planning pregnancy.
* Travel plans that do not permit full participation.
* Inability to walk without assistance. The capability to walk upright is fundamental because accelerometry measures the duration and intensity of horizontal physical activities.
* Inability to give consent.
40 Years
60 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
USDA Grand Forks Human Nutrition Research Center
FED
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
James Roemmich, PhD
Role: PRINCIPAL_INVESTIGATOR
USDA-ARS-GFHNRC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Grand Forks Human Nutrition Research Center
Grand Forks, North Dakota, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Jahns L, Johnson LK, Conrad Z, Bukowski M, Raatz SK, Jilcott Pitts S, Wang Y, Ermakov IV, Gellermann W. Concurrent validity of skin carotenoid status as a concentration biomarker of vegetable and fruit intake compared to multiple 24-h recalls and plasma carotenoid concentrations across one year: a cohort study. Nutr J. 2019 Nov 21;18(1):78. doi: 10.1186/s12937-019-0500-0.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
GFHNRC018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.