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Eine Studie entspricht den Filterkriterien
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HealthyTogether: RCT of a Dyadic Weight Management Intervention

Offene Rekrutierung
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT06619041 ist eine interventionsstudie zur Untersuchung von Fettleibigkeit, Übergewicht und hat den Status offene rekrutierung. Die Studie startete am 14. Juli 2025 und soll 320 Teilnehmer aufnehmen. Durchgeführt von VA Office of Research and Development ist der Abschluss für 30. September 2028 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 16. Juli 2025 aktualisiert.
Kurzbeschreibung
Four in five Veterans have overweight or obesity. However, few eligible Veterans achieve meaningful weight loss in VA's national MOVE! Weight Management Program. Family and friends strongly influence a person's health behaviors and weight. Including a close family member or friend in weight management may improve weight management outcomes. This study will test whether an 14-week, 8-session virtual weight management program that includes Veterans and a support person (e.g., family member or friend) leads to weight loss. The investigators will also test whether the program leads to improvements in weight-related health behaviors, including physical activity and diet, and relationship quality.
Ausführliche Beschreibung
The prevalence of overweight and obesity is more than 80% among VA users, increasing risk of morbidity and mortality. In 2006, VA nationally implemented the MOVE! Weight Management Program, an evidence-based behavioral weight management program. Effectiveness of MOVE! is suboptimal: <20% of all participants and only 30% of those with intense and sustained participation achieve clinically meaningful weight loss. Furthermore, only 8-9% of eligible Veterans attend any MOVE! sessions and, among those who do, half attend only a single session. Taken together, <2% of the 3.2 million eligible Veterans lose clinically meaningful weight in MOVE!. Therefore, additional weight management approaches are needed to address obesity at the VA population-level.

One strategy to improve behavioral weight management effectiveness is by leveraging social relationships. Social support improves weight management program initiation, retention, and short and long-term weight loss and is also a major driver of weight-related behaviors, such as physical activity and diet quality. However, social relationships can also impede weight management, for example, when close others (e.g., family and friends) undermine or do not support behavior change. The key to addressing this double-edged sword of social relationships may be through dyadic approaches that include close others in behavioral weight management with a focus on improving communication and relationship quality.

HealthyTogether is a brief, virtual weight management program for Veterans and a close other ("partner"). Over 14 weeks, individual dyads receive 8 hour-long video sessions with a clinician. Session content includes physical activity, diet, and weight management medication education; goal setting; and relationship and communication skills training and practice, informed by evidence-based dyadic treatments. This study is a two-site hybrid type I effectiveness-implementation randomized controlled trial with a primary focus on evaluating effectiveness of HealthyTogether and a secondary focus on understanding determinants of implementation. The aims of the trial are:

  1. Test whether HealthyTogether results in greater weight loss than usual care at 6 months among Veterans (primary).
  2. Examine differences between HealthyTogether and usual care groups in secondary Veteran and partner outcomes, including health behaviors (i.e., diet, physical activity) and relationship quality.
  3. Examine Veteran and partner contributions to changes in their own and each other's outcomes using dyadic analyses, informing potential future intervention targets.
  4. Assess determinants of implementation, including cost, feasibility, acceptability, and appropriateness, guided by the Consolidated Framework for Implementation Research, to inform future implementation.

Considering the burden of overweight and obesity in VA and the limited reach and effectiveness of MOVE!, HealthyTogether has the potential to address multiple VA priorities: mitigate obesity-related chronic disease and involve family in Veterans' care. Study findings will inform VA National Center Health for Health Promotion and Disease Prevention efforts to expand effective, evidence-based weight management services for Veterans.

Offizieller Titel

Harnessing the Power of Social Support for Weight Management: a Randomized Controlled Trial of HealthyTogether

Erkrankungen
FettleibigkeitÜbergewicht
Weitere Studien-IDs
  • IIR 23-040
NCT-Nummer
Studienbeginn (tatsächlich)
2025-07-14
Zuletzt aktualisiert
2025-07-16
Studienende (vorauss.)
2028-09-30
Geplante Rekrutierung
320
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Offene Rekrutierung
Stichwörter
Weight Loss
Weight Loss Programs
Social Support
Diet
Physical Activity
Virtual Medicine
Family
Dyadic
Primäres Ziel
Versorgungsforschung
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Einfach verblindet
Studienarme/Interventionen
Teilnehmergruppe/StudienarmIntervention/Behandlung
ExperimentellTreatment Arm
Receives the brief, virtual, dyadic HealthyTogether weight management intervention in addition to usual care.
Healthytogether
HealthyTogether is a brief (8-session), virtual, dyadic weight management intervention.
Keine InterventionUsual Care Arm
Receives a brief letter with information about weight management and couples/family resources in addition to usual care.
Nicht zutreffend
Hauptergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Change in weight from Baseline to 6-months among Veterans
Weight is measured using a study-provided scale during a scheduled virtual study visit. Veterans will either (1) display the weight on the scale to study staff or (2) take a picture of the weight on the scale with a digital device and show the weight to study staff. For weight measurements at both timepoints, we will instruct participants to weigh themselves in light clothing and no shoes, with the scale on a hard, flat surface. We will record date and time of weight assessments and will make every attempt to collect follow-up weights at a similar time of day as baseline.
6-months
Nebenergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Change in weight from Baseline to 6-months among Veterans (including EHR-data)
We will collect supplementary EHR-based weights from for all Veteran participants. We will use the EHR weight closest to 182 days +/- 60 days post-baseline. While the primary outcome is limited to Veterans with study team measured weight, secondary analyses will be conducted among all participants with available weight outcomes (staff verified and/or EHR-based).
6-months
Change in weight from Baseline to 6-months among partners
Weight is measured using a study-provided scale during a scheduled virtual study visit. Partners will either (1) display the weight on the scale to study staff or (2) take a picture of the weight on the scale with a digital device and show the weight to study staff. We will record date and time of weight assessments and will make every attempt to collect follow-up weights at a similar time of day as baseline.
6-months
Change in weight from Baseline to 12-months among Veterans (using EHR data)
Baseline weight is measured using a study-provided scale during a scheduled virtual study visit. To examine durability of intervention effects while minimizing participant burden, we will also obtain EHR-based weights at 12 months, using weights collected 365 days +/- 90 days post-baseline among only Veterans.
12-months
Change in self-reported diet quality from Baseline to 6-months among Veterans
This outcome is measured by self-report using the eight-item Starting the Conversation measure.
6-months
Change in self-reported diet quality from Baseline to 6-months among partners
This outcome is measured by self-report using the eight-item Starting the Conversation measure.
6-months
Change in physical activity from Baseline to 6-months among Veterans
This outcome is measured by self-report using the 9-item International Physical Activity Questionnaire-Short Form.
6-months
Change in physical activity from Baseline to 6-months among partners
This outcome is measured by self-report using the 9-item International Physical Activity Questionnaire-Short Form.
6-months
Change in relationship quality from Baseline to 6 months among Veterans
This outcome is assessed by self-report with the seven-item Relationship Assessment Scale, revised for non-romantic relationships.
6-months
Change in relationship quality from Baseline to 6 months among partners
This outcome is assessed by self-report with the seven-item Relationship Assessment Scale, revised for non-romantic relationships.
6-months
Eignungskriterien

Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle
Akzeptiert gesunde Freiwillige
Ja

Veteran participants:

  • Age 18 or higher.
  • Assigned to a VA primary care provider.
  • Have a weight measurement (BMI>=30) recorded in the VA medical record within 16 weeks prior to enrollment.
  • Have a second, valid weight measurement recorded in the VA medical record within the prior year.
  • Have a BMI>=30 at enrollment.
  • Able to participate in virtual intervention sessions during regular business hours.

Partner participants:

  • Age 18 or higher.
  • Able to participate in virtual intervention sessions during regular business hours.
  • Speak with Veteran at last weekly.

Veterans are excluded if:

  • not fluent in English
  • have severe hearing loss prohibiting participation
  • have a dementia diagnosis
  • have recently (within the past 3 months) participated in a clinical or research behavioral weight management program
  • have a history of or plans (within 6 months) to have bariatric surgery
  • are pregnant, postpartum, nursing, or planning to become pregnant within 6 months
  • are receiving cancer (non-skin) treatment
  • have drug or alcohol dependence not in remission, a recent suicide attempt, active psychosis, or an active behavior flag in the medical record
  • report high-levels of alcohol use (AUDIT-C score >=8)
  • are receiving hospice or palliative care
  • are living in a nursing home or assisted living facility
  • are enrolled in VA home-based primary care
  • have end stage renal disease
  • have a current or past diagnosis of anorexia or bulimia
  • have had an inpatient hospitalization in the past 3 months
  • weigh more than 440 pounds (this is the upper limit of the study's scales)

Partners are excluded if:

  • not fluent in English
  • have severe hearing loss prohibiting participation
  • endorse having a health condition that may limit their ability to participate in the intervention
  • report high-levels of current alcohol use (AUDIT-C score >=8)
  • are receiving hospice or palliative care
  • are living in a nursing home or assisted living facility
VA Office of Research and Development logoVA Office of Research and Development
Zentrale Studienkontakte
Kontakt: Kristen E Gray, PhD MS BS, (206) 764-2056, [email protected]
Kontakt: Katherine D Hoerster, PhD MPH BA, (206) 277-4203, [email protected]
2 Studienstandorte in 1 Ländern

Colorado

Rocky Mountain Regional VA Medical Center, Aurora, CO, Aurora, Colorado, 80045-7211, United States
Luis M Perez, PhD RD, Kontakt, 719-244-4805, [email protected]
Briana Robustelli, Kontakt, (720) 723-6872, [email protected]
Luis M Perez, PhD RD, Prüfarzt
Offene Rekrutierung

Washington

VA Puget Sound Health Care System Seattle Division, Seattle, WA, Seattle, Washington, 98108-1532, United States
William A Banks, MD, Kontakt, 206-764-2701, [email protected]
Steven B Zeliadt, PhD MPH, Kontakt, (206) 277-4175, [email protected]
Kristen E. Gray, PhD MS BS, Hauptprüfer
Noch nicht rekrutierend