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Ideas Moving Parents and Adolescents to Change Together (IMPACT) (IMPACT)

13 agosto 2020 aggiornato da: Elaine Borawski, Case Western Reserve University

Targeting Obesity and Blood Pressure in Urban Youth(Consortium Title: Childhood Obesity Prevention and Treatment Research [COPTR] and Site Project Name IMPACT (Ideas Moving Parents and Adolescents to Change Together).

The National Heart, Lung, and Blood Institute (NHLBI) of the National Institute of Health (NIH) has sponsored a consortium of four sites across the United States, entitled Childhood Obesity Prevention and Treatment Research (COPTR). Each site has its own protocol. Case Western Reserve/Cleveland's project is entitled "Targeting Obesity and Blood Pressure in Urban Youth". The site name is IMPACT (Ideas Moving Parents and Adolescents to Change Together).

The project assesses the effects of three interventions on Body Mass Index(BMI) in overweight and obese urban 5th-8th grade youth: a cognitive-behavioral intervention (HealthyChange), a systems improvement intervention (SystemsChange), and an education-only intervention (Tools4Change). In addition the study assesses the potential additional impact of a school-community based intervention on outcomes.

The project has two phases: a formative phase (including focus groups and a pilot) and the main trial. The main trial will take place over approximately four years.

Panoramica dello studio

Stato

Completato

Condizioni

Descrizione dettagliata

The IMPACT trial will involve a 3-arm randomized controlled trial of three behavioral and educational interventions: (1) HealthyCHANGE, a behavioral approach focusing on building skills and increasing intrinsic motivation (based on cognitive-behavioral theory with motivational interviewing components); (2) SystemCHANGE, an innovative behavioral approach focusing on system re-design of the family environment and daily routines (based on social-ecological and personal process improvement theories); and (3) education-only (representing usual care, called Tools4CHANGE).

In the main trial, approximately half of the children will also be in schools that take part in the We Run This City (WRTC)Marathon program, a school-based fitness program administered by the YMCA, and half will be in schools that do not take part in the WRTC program.

This study will assess the impact of the interventions on the main trial's (1) primary outcome, Change in Body Mass Index (BMI). (2) secondary outcomes including diet, physical activity, sedentary behavior, sleep, blood pressure, cardiovascular risk, body composition, fitness, and quality of life (3) mediators including : child's self-efficacy, social support, motivation, family problem solving ability, systems thinking, and self-regulation;(4) moderators including: socioeconomic status, demographic factors, environmental factors, personal and psychosocial characteristics of child and parent.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

360

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Ohio
      • Cleveland, Ohio, Stati Uniti, 44106
        • Case Western Reserve University

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 11 anni a 15 anni (Bambino)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • Students entering the 6th grade who are found at the standard school screenings to be overweight or obese
  • (BMI 85th- 94th percentile or > 95th percentile for age/sex respectively)

Exclusion Criteria:

  • Taking medications that alter appetite or weight (e.g. glucocorticoids, metformin, insulin, Risperidone (Risperdal), Olanzapine (Zyprexa), Clozapine(Clozaril), Quetiapine (Seroquel), Ziprasidone (Geodon), Carbamazepine (Tegretol), Valproic acid (Depakote/Depakene/Depacon), Aripiprazole (Abilify), Orlistat (Xenical), Sibutramine (Meridia), Phentermine, Diethylproprion (Tenuate), Topirimate (Topamax), glitazones (thiazolidinediones)
  • Inability to understand English
  • Stage 2 hypertension or stage 1 hypertension with end organ damage (left ventricular hypertrophy, microalbuminuria)
  • Severe behavioral problems that preclude group participation (as reported by parent/guardian)
  • Child involvement in another weight management program
  • Family expectation to move from the region within 1 year
  • The presence of a known medical condition that itself causes obesity (e.g., Prader-Willi syndrome) or interfere with HbA1C ( sickle cell disease)

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: HealthyCHANGE
Cognitive behavioral strategies to address diet, physical activity, sedentary behavior and sleep for children.

Cognitive behavioral strategies to address diet, physical activity, sedentary behavior and sleep for children.

It involves an intensive series of group sessions, followed by rotating monthly face-to-face meetings or phone calls.

Sperimentale: SystemCHANGE
Intervention (based on systems improvement and choice architecture theories) System improvement and choice architecture theories seek to teach a set of skills using family self-designed experiments to redesign daily routines

Intervention (based on systems improvement and choice architecture theories) System improvement and choice architecture theories seek to teach a set of skills using family self-designed experiments to redesign daily routines regarding eating, activity and sleep.

It involves an intensive series of group sessions, followed by rotating monthly face-to-face meetings or phone calls.

Nessun intervento: Tools4CHANGE
In contrast to the behavioral arms, youths with their parent(s)/guardian randomized to this group will have one 60-minute face-to-face meeting at initiation of the study with a dietitian who is also trained in recommendations for exercise and sedentary behavior.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Slope of Body Mass Index (BMI)
Lasso di tempo: Baseline, 12 mos, 24 mos and 36 mos
BMI slope (trajectory over 3 years) was created for each participant with outcomes multiply imputed for children without BMI values post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.
Baseline, 12 mos, 24 mos and 36 mos

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Dietary Intake- Calories Per Day
Lasso di tempo: Baseline, 12 mos, 24 mos and 36 mos

Annualized change in calories per day.

Dietary intake slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without diet recall data post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Baseline, 12 mos, 24 mos and 36 mos
Blood Pressure
Lasso di tempo: Baseline, 12 mos, 24 mos and 36 mos

Annualized change in blood pressure measures using the slope of 3 year trajectory.

Blood pressure slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without blood pressure readings post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Baseline, 12 mos, 24 mos and 36 mos
Physical Activity
Lasso di tempo: [Baseline, 12 mos, 24 mos and 36 mos]

Annualized change in physical activity measures of moderate to vigorous minutes per day and bed rest/sedentary minutes per day as measured by accelerometer.

Physical activity slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without accelerometer readings post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

[Baseline, 12 mos, 24 mos and 36 mos]
Sleep
Lasso di tempo: [Baseline, 12 mos, 24 mos and 36 mos]

The results reflect the annualized change in adolescent sleep wake scale and pediatric daytime sleepiness scale. The items of the adolescent sleep wake scale are recoded to have a minimum of 0 and maximum value of 5, in which a higher scores for both the individual items and the overall sum score indicate a better outcome. The items of the pediatric daytime sleepiness are recoded to have a minimum of 0 and maximum value of 4, in which a lower score for both the individual items and the overall sum score indicates a better outcome.

Sleep slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without post-baseline measures. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

[Baseline, 12 mos, 24 mos and 36 mos]
Cardiometabolic Factors- Fasting Glucose, HDL Cholesterol, LDL Cholesterol, Total Cholesterol
Lasso di tempo: Baseline, 12 mos, 24 mos and 36 mos

Annualized change in various cardiometabolic factor measures over 3 years.

Cardiometabolic factor slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without blood draws post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in the slopes of fasting glucose, HDL cholesterol, LDL cholesterol, and total cholesterol over 3 years reported.

Baseline, 12 mos, 24 mos and 36 mos
Body Composition- BMI Percentile
Lasso di tempo: Baseline, 12 mos, 24 mos and 36 mos

The annualized change in body composition measures over 3 years.

Body composition slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without body composition measurements post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in slope of BMI percentile over time reported.

Baseline, 12 mos, 24 mos and 36 mos
Fitness
Lasso di tempo: Baseline, 12 mos, 24 mos and 36 mos

The annualized change in pacer laps completed during PACER test over 3 years.

PACER test slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without PACER test measurements post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Baseline, 12 mos, 24 mos and 36 mos
Quality of Life- Perceived Stress
Lasso di tempo: [Baseline, 12 mos, 24 mos and 36 mos]

The annualized change in perceived stress over 3 years. Participants are asked to rate individual scale items on their perception of how often they feel specific stressors on a scale from 0 (never) to 4 (very often). Individual scale items are summed for a total score. Higher scores indicate higher perceived frequency of stressors, therefore higher perceived stress. Outcomes are reported as the mean of the slope estimates for total perceived stress score over 3 years (from baseline to 36 months).

The perceived stress slope (trajectory over 3 years) was created for each participant with outcomes multiply imputed for children without stress scores post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

[Baseline, 12 mos, 24 mos and 36 mos]
Dietary Intake- Percent Calories From Fat
Lasso di tempo: Baseline, 12 months, 24 months, 36 months

The annualized change of percent of calories from fat over 3 years.

Percent calories from fat slope (trajectory over 3 years) was created for each participant with outcomes multiply imputed for children without diet recall data post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Baseline, 12 months, 24 months, 36 months
Dietary Intake- Fruit and Vegetable Servings
Lasso di tempo: Baseline, 12 months, 24 months, 36 months

The annualized change in the number of fruit and vegetable servings per day over 3 years.

Serving slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without diet recall data post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Baseline, 12 months, 24 months, 36 months
Dietary Intake- Sodium
Lasso di tempo: Baseline, 12 months, 24 months, 36 months

The annualized change in sodium intake (mg) per day over 3 years.

Sodium intake slope (trajectory over 3 years) was created for each participant with outcomes multiply imputed for children without diet recall data post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Baseline, 12 months, 24 months, 36 months
Cardiometabolic Factors- Hemoglobin A1c
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

Annualized change in various cardiometabolic factor measures over 3 years.

Cardiometabolic factor slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without blood draws post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in the slope of glycated Hemoglobin A1c over 3 years reported.

[Baseline, 12 mos, 24 mos, 36 mos]
Cardiometabolic Factors- High-sensitivity C-reactive Protein
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

Annualized change in various cardiometabolic factor measures over 3 years.

Cardiometabolic factor slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without blood draws post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in the slope of high-sensitivity C-reactive protein over 3 years reported.

[Baseline, 12 mos, 24 mos, 36 mos]
Cardiometabolic Factors- Insulin
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

Annualized change in various cardiometabolic factor measures over 3 years.

Cardiometabolic factor slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without blood draws post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in the slope of insulin over 3 years reported.

[Baseline, 12 mos, 24 mos, 36 mos]
Cardiometabolic Factors- HOMA-IR
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

Annualized change in various cardiometabolic factor measures over 3 years.

Cardiometabolic factor slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without blood draws post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in the slope of HOMA-IR over 3 years reported.

[Baseline, 12 mos, 24 mos, 36 mos]
Body Composition- Waist-to-height Ratio
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

The annualized change in body composition measures over 3 years.

Body composition slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without body composition measurements post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in slope of waist-to-height ratio over time reported. The weight-to-heigh ratio compares the child's waist circumference (cm) to their height (cm).

[Baseline, 12 mos, 24 mos, 36 mos]
Body Composition- Waist Circumference
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

The annualized change in body composition measures over 3 years.

Body composition slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without body composition measurements post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in slope of waist circumference (cm) over time reported.

[Baseline, 12 mos, 24 mos, 36 mos]
Body Composition- Percent Body Fat
Lasso di tempo: [Baseline, 12 mos, 24 mos, 36 mos]

The annualized change in body composition measures over 3 years.

Body composition slopes (trajectory over 3 years) were created for each participant with outcomes multiply imputed for children without body composition measurements post-baseline. An F test with two numerator degrees of freedom was used to test for between-group differences using an alpha of .05.

Change in slope of body fat percentage over time reported. Body fat percentage calculated using Stevens equation.

[Baseline, 12 mos, 24 mos, 36 mos]

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Elaine A Borawski, PhD, Case Western Reserve University
  • Investigatore principale: Shirley M Moore, RN, PhD, Case Western Reserve University

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 febbraio 2011

Completamento primario (Effettivo)

21 gennaio 2017

Completamento dello studio (Effettivo)

31 gennaio 2017

Date di iscrizione allo studio

Primo inviato

20 dicembre 2011

Primo inviato che soddisfa i criteri di controllo qualità

17 gennaio 2012

Primo Inserito (Stima)

23 gennaio 2012

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

25 agosto 2020

Ultimo aggiornamento inviato che soddisfa i criteri QC

13 agosto 2020

Ultimo verificato

1 agosto 2020

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • IMPACT-1-5U01HL103622-02
  • 5U01HL103622-02 (Sovvenzione/contratto NIH degli Stati Uniti)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Sì

Descrizione del piano IPD

Conducted in conjunction with the Research Coordinating Unit (UNC Chapel Hill) of the COPTR Consortium.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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