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Development of Novel Behavioral Intervention for Sustainable Weight Loss in Hispanic Adults With Obesity

17 luglio 2020 aggiornato da: Maria Carlota Dao, Tufts University

There are great disparities in the prevalence of obesity and chronic disease in different sociodemographic groups. US Hispanic adults, in particular, have a higher prevalence of obesity and chronic diseases than non-Hispanic whites. Population aging is also a major contributing factor to the high prevalence of chronic disease, and Hispanics already make up approximately 10% of the older population. Therefore, preventive measures are needed to reduce the burden of chronic disease risks for Hispanics. Current lifestyle interventions for weight management have been particularly ineffective in this population.

The purpose of this pilot project is to develop a novel tailored lifestyle intervention for use by Hispanic older adults with obesity. The Healthy Weight for Living intervention has been validated among adults with mixed racial/ethnic backgrounds and has achieved clinically impactful weight-loss. Its design features make it particularly suitable for use in populations with low adherence to traditional interventions, including no requirement for daily food logging and no increase in physical activity.

The final product of this project will be a culturally adapted prototype intervention in Hispanic older adults that accounts for cultural heterogeneity. This work has direct relevance to reducing health disparities and the burden of obesity-associated chronic disease in a particularly at-risk population.

Panoramica dello studio

Stato

Terminato

Condizioni

Descrizione dettagliata

The scientific premise of this project is that appropriately tailored lifestyle interventions for weight loss can achieve clinically impactful weight loss in Hispanic adults with obesity. Older adults will be the focus, recognizing that requirements for tailoring may vary according to age group. Given that older adults have a higher risk of chronic diseases caused by obesity, there is a great need to focus on factors that disproportionately affect older Hispanic adults. The objective of this project is to tailor a validated lifestyle intervention developed and used by our team in ethnically mixed populations to older Hispanic adults with obesity. This novel intervention does not require food logging or a large increase in physical activity to achieve weight loss, making it more acceptable to population groups with low adherence to traditional interventions. The long-term goal of this work is to create an effective, culturally acceptable, sustainable, and scalable lifestyle weight management program for routine use in Hispanic adults with obesity. Findings from this work will be directly applicable to future community interventions and will be relevant for public health measures in this at-risk population.

The specific aims are:

Aim 1: To conduct focus groups in Hispanic older adults with obesity to identify factors that can be addressed in the tailored intervention. Information will be collected on practical and cultural barriers and promoters of successful weight management, including food access, dietary patterns, physical activity, time and financial constraints, and additional psychosocial and cultural factors.

Hypothesis 1: Malleable dietary and psychosocial targets for weight loss and weight loss maintenance can be identified, including factors such as food cravings, hunger and disinhibited eating that have been shown to be effective targets in other population groups.

Aim 2: To conduct a pilot behavioral intervention of an initially adapted program in Hispanic older adults with obesity. A prototype bilingual English-Spanish lifestyle intervention for weight reduction will be created. The prototype will then be iteratively refined during a series of short-term tests (two tests lasting 4 weeks, followed by a final test lasting 12 weeks) of intervention delivery. In these interventions, % weight loss, % drop-out, and safety benchmarks will be monitored. Participant-reported barriers to adherence identified during group meetings and exit interviews will be targets for improvement in successive iterations.

Hypothesis 2: Successive refinement of the program will result in progressive improvements in mean % weight loss and participant retention.

The final products of this project will be: a) a prototype adapted intervention in older US adults of Hispanic background, accounting for cultural heterogeneity in this population; and b) identification of additional barriers that can be addressed in subsequent iterations of the intervention.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

23

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

    • Massachusetts
      • Boston, Massachusetts, Stati Uniti, 02111
        • Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts 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

50 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

INCLUSION CRITERIA:

Focus groups and Intervention:

  1. Adult men and women older than 50 years.
  2. Self-identifying as having Hispanic ethnicity, originating from Spanish-speaking Latin-American country.
  3. BMI ≥30.0 kg/m2.

    Intervention only:

  4. Willing to give informed consent.
  5. All individuals wishing to participate in the intervention part of this study will be required to agree to inform their physician prior to enrollment and to notify the Tufts team if their physician recommends against weight loss for any reason. A physician's clearance form will be provided by Tufts to all participants wishing to enroll in the intervention. Participants will be required to obtain their physicians' signature and their physician will send the completed form to us. We will enroll them only after we have obtained a signed physician clearance form.
  6. Willing to participate in a behavioral intervention for weight loss.

EXCLUSION CRITERIA:

Intervention only:

  1. Self-reported weight loss >5 kg within past 6 months.
  2. Diagnosed gastrointestinal conditions, including celiac disease.
  3. Communicable or chronic diseases or medication use that would preclude safe and active study participation.
  4. Pregnancy or anticipated pregnancy within the study,
  5. Lactation, or giving birth within 6 months prior to enrollment.
  6. Participation in other clinical trials.
  7. Illiteracy.
  8. Use of anti-obesity medications within the past year.
  9. Being on any special diets that would prevent following recommendations made through the program.

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: Non randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Nessun intervento: Focus groups

Information on practical and cultural barriers and promoters of successful weight management will be collected through focus groups. This will include include food access, dietary patterns, physical activity, time and financial constraints, and additional psychosocial and cultural factors.

A total of 30 participants will be recruited for the focus groups.

Sperimentale: Pilot behavioral intervention
A prototype bilingual English-Spanish lifestyle intervention for weight reduction will be created. The prototype will then be iteratively refined during a series of short-term tests with 5 participants per test (two tests lasting 4 weeks, followed by a final test lasting 12 weeks) of intervention delivery.

The Healthy Weight for Living (HWL) intervention, previously developed at the Energy Metabolism Laboratory (HNRCA), is broadly informed by the same behavior change theories as other interventions. For example, it also recognizes individual and environmental factors as potential areas to support behavior change for weight regulation, and provides practical tools for facilitating new habits. However, the HWL places greater emphasis on the role of biology in influencing eating behavior, giving a central role to hunger and food cravings as modulators of eating behavior. Therefore, HWL does not emphasize self-monitoring food intake and does not require increasing physical activity for effectiveness. The new intervention also targets autonomous motivation and prioritizes ease of implementation.

Information from focus groups and sequential pilots will be used to develop a culturally tailored prototype version of Healthy Weight for Living that is acceptable for Hispanic older adults.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Weight change
Lasso di tempo: Pilot 1 and 2: 4 weeks. Pilot 3: 12 weeks
Change in weight from baseline to the end of the intervention period
Pilot 1 and 2: 4 weeks. Pilot 3: 12 weeks
Attendance to weekly group meetings
Lasso di tempo: Pilot 1 and 2: 4 weeks. Pilot 3: 12 weeks
Adherence will be measured as meeting attendance
Pilot 1 and 2: 4 weeks. Pilot 3: 12 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in blood pressure (systolic and diastolic)
Lasso di tempo: Depending on pilot phase the time frame will be 4 weeks or 12 weeks
Change in systolic and diastolic blood pressure from baseline to the end of the intervention period
Depending on pilot phase the time frame will be 4 weeks or 12 weeks
Change in waist circumference
Lasso di tempo: Depending on pilot phase the time frame will be 4 weeks or 12 weeks
Change in waist circumference from baseline to the end of the intervention period
Depending on pilot phase the time frame will be 4 weeks or 12 weeks
Change in hip circumference
Lasso di tempo: Depending on pilot phase the time frame will be 4 weeks or 12 weeks
Change in hip circumference from baseline to the end of the intervention period
Depending on pilot phase the time frame will be 4 weeks or 12 weeks
Themes generated from qualitative data
Lasso di tempo: Baseline, 4 weeks for pilot cycles 1 and 2, and 12 weeks for pilot cycle 3

For the first phase of the study, focus groups will be analyzed and themes on eating behavior and barriers to successful weight management will be identified.

For the intervention phase of the study, exit interviews will be completed at the end of each pilot cycle.

Baseline, 4 weeks for pilot cycles 1 and 2, and 12 weeks for pilot cycle 3
Financial well-being
Lasso di tempo: Baseline
Financial well-being questionnaire (4 items). Financial satisfaction (1 item) Financial difficulty (1 item) Financial control (1 item) Scores are standardized and summed to capture financial well-being. Higher scores indicate more financial well-being.
Baseline
Dietary intake
Lasso di tempo: Baseline

NHANES Dietary Screener Questionnaire (DSQ, 26 items). The DSQ scoring algorithms developed at the National Cancer Institute will be used to calculate estimated intakes of food groups and certain nutrients: fruits and vegetables (cup equivalents), dairy (cup equivalents), added sugars (teaspoon equivalents), whole grains (ounce equivalents), and fiber (g).

Source: https://epi.grants.cancer.gov/nhanes/dietscreen/scoring/current/#scoring

Baseline
Dietary behavior
Lasso di tempo: Baseline

Latino Dietary Behaviors Questionnaire (LDBQ, 13 items)

Possible scores:

Health dietary changes score range: 0 to 19 Artificial sweeteners in drinks score range: 0 to 13 Number of meals per day score range: 0 to 6 Fat consumption score range: 0 to 9 Total LDBQ score range (sum of all items): 0 to 47 Lower scores indicate poorer dietary behaviors.

Baseline
Perceived stress
Lasso di tempo: Baseline
Perceived Stress Scale 4 (PSS-4, 4 items) Score range: 0 to 16. Higher scores are correlated to more stress.
Baseline
Eating behavior (hunger, satiety, cognitive restraint)
Lasso di tempo: Baseline
Three factor eating questionnaire (TFEQ, 51 items) Cognitive restraint score range: 0 to 21 Disinhibition score range: 0 to 16 Hunger score range: 0 to 14 Higher scores indicate higher degrees of the particular eating behavior.
Baseline
Acculturation
Lasso di tempo: Baseline
Short Acculturation Scale for Hispanics (SASH, 12 items) Each item response is based on a five-point bipolar scale. Scores are calculated by taking the average rating across all items. Higher scores indicate higher acculturation.
Baseline

Collaboratori e investigatori

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

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)

23 agosto 2019

Completamento primario (Effettivo)

16 luglio 2020

Completamento dello studio (Effettivo)

16 luglio 2020

Date di iscrizione allo studio

Primo inviato

3 giugno 2019

Primo inviato che soddisfa i criteri di controllo qualità

5 giugno 2019

Primo Inserito (Effettivo)

7 giugno 2019

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

21 luglio 2020

Ultimo aggiornamento inviato che soddisfa i criteri QC

17 luglio 2020

Ultimo verificato

1 luglio 2020

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

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

NO

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

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 .

Prove cliniche su Healthy Weight for Living for Hispanics

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