- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02691039
NEW Keiki Family Based Intervention to Combat Childhood Obesity
N.E.W. Keiki - Nutrition + Exercise + Weight Management Programs: Family-based Intervention to Combat Childhood Obesity in Hawai'i
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
A database containing pre and post program information will be developed. For the referred patients, this database will contain information related to the following:
- Past medical history
- Obesity-related Medical co-morbidities (HTN, hyperlipidemia, e.g.)
- Lab values (fasting lipids, glucose, LFTs, HbA1c)
- Anthropometric data (ht, weight, BMI) and select vital signs (BP, HR)
- Fitness testing data
- Demographic data (age, gender, ethnicity, socioeconomic status, geographical address)
- Answers to a lifestyle, attitudes, and health habits survey
- Answers to a program survey
- Contact information for follow up
For participating family members (parents, grandparents, siblings, e.g.) this data base will contain information related to the following:
- Past medical history
- Obesity-related Medical co-morbidities (HTN, hyperlipidemia, e.g.)
- Anthropometric data (ht, weight, BMI) and select vital signs (BP, HR)
- Demographic data (age, gender, ethnicity, socioeconomic status, geographical address)
- Answers to a lifestyle, attitudes, and health habits survey
- Answers to a program survey
- Contact information for follow up
Once the database is created a retrospective chart review will be done to collect data on patients that have completed the program. This information will be obtained from facility records and program records. Individuals who previously completed the program will be contacted and asked to provide consent to be included in the database. Only data from individuals who provide consent will be included in the database.
Participants in the program will be asked to provide consent when they enroll in the program or when they come for a follow up visit. Only data from individuals who provide consent will be included in the database.
Subjects will be followed to collect information on lifestyle maintenance and long term health outcomes.
The database will be queried regularly to provide information about the participants and program.
Descriptive statistics will be calculated to describe the study population pre and post program. Outcomes will be analyzed using appropriate statistical tests. Exploratory analysis will be conducted to detect trends.
Data will be stored in a secure location with limited access. All paper documents will be stored in a locked office in a locked cabinet. Electronic data will be stored on a limited access computer. The database will be password protected and encrypted.
All participants will be assigned a study ID number. The study ID will be used for transmission of data. Data collection forms will use the assigned study ID. All data that needs to be transmitted will be de-identified to the extent possible, password protected, and encrypted.
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
-
-
Hawaii
-
Honolulu, Hawaii, Vereinigte Staaten, 96826
- Kapiolani Medical Center for Women and Children
-
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- current or past participant in the NEW Keiki program
- participating family member
- able to understand English
Exclusion Criteria:
- do not meet inclusion criteria
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Beobachtungsmodelle: Familienbasiert
- Zeitperspektiven: Sonstiges
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Composite measure of improvement in participant/family health to include change in Body Mass Index, Weight, Blood Pressure, Lab Values
Zeitfenster: minimum 1 year
|
Change in body mass index (BMI),change in weight, change in blood pressure (BP), change in lab values
|
minimum 1 year
|
Composite measure of improvement in participant/family health to include change in lifestyle survey
Zeitfenster: minimum 1 year
|
Change in lifestyle survey about diet/nutrition and behaviors
|
minimum 1 year
|
Composite measure of improvement in participant/family health to include change in fitness testing data
Zeitfenster: minimum 1 year
|
Change in fitness testing data
|
minimum 1 year
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Malia Shimokawa, MD, Kapiolani Medical Center for Women & Children
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2013-075
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Produkt, das in den USA hergestellt und aus den USA exportiert wird
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