POWERSforID: A Telehealth Weight Management System for Adults With Intellectual Disability (POWERSforID)
13. november 2018 opdateret af: James Rimmer, University of Alabama at Birmingham
POWERSforID: Personalized Online Weight and Exercise Response System for Adults With Intellectual Disability
POWERSforID is a 24 week randomized control trial designed to assess the feasibility of a telehealth and coaching intervention for improving health outcomes of adults with intellectual disability.
Recruitment is conducted through a disability health clinic located in Colorado Springs, CO.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
POWERS (Personalized Online Weight and Exercise Response System) platform is a novel, multifocal-centered tailored intervention utilizing an innovative online tool designed to facilitate improvements in physical activity and nutritional behaviors.
Aim 1 of this protocol is to customize the POWERS platform, demonstrated effective in previous research, for adults with intellectual disability (ID) and their caregivers to be referred to as POWERSforID.
The POWERSforID intervention is designed to achieve weight loss and improve specific health markers while respecting and supporting the needs of the participants with ID as well as their caregivers.
Aim 2 of the project is to conduct a pilot study to assess the usability and feasibility of the POWERSforID system and intervention with 5 adults with ID and their caregiver and improve the system based on pilot data.
Aim 3 of the protocol is to conduct a randomized controlled trial (RCT) to examine the effect of POWERSforID on educating and coaching caregivers about nutrition and exercise and thus improving health status and reducing body weight in obese adults with ID.
The investigators hypothesize that the obese participants in the intervention group (POWERSforID) will evidence significantly greater weight loss and improved health status (i.e.
lower waist circumference, blood pressure, decreased body fat percentage, and improved blood lipids) compared to a control group.
The investigators also hypothesize that both adults with ID and their caregivers will demonstrate improved knowledge, attitudes, and self-efficacy related to diet and exercise.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
36
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Alabama
-
Birmingham, Alabama, Forenede Stater, 35292
- University of Alabama at Birmingham
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
25 år til 50 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
Participants with intellectual disability (ID) who meet the following inclusion criteria are eligible to participate in the study:
- Body Mass Index > or equal to 30 kg/m2;
- Diagnosis of mild or moderate ID;
- 25 to 50 years of age;
- Medical provider approval to participate in a weight loss program;
- Has a caregiver who agrees to participate in the study and provides services 4 days a week or more to the adult with ID;
- Has access to a computer with internet throughout the week.
Exclusion Criteria:
- Currently on a weight loss program;
- Medical conditions that prevent participation as noted by the medical provider or legal guardian including heart and/or renal disease;
- Behavioral issues determined by the DDHC Behavioral Health staff;
- Unable to walk or exercise due to a mobility impairment or medical condition;
- Judged to have insufficient capacity to consent or assent as assessed using the "Supplemental Consent Document".
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: POWERSforID
POWERSforID intervention group
|
Feasibility and outcomes associated with use of the POWERSforID system and coaching phone calls over the course of 24 weeks
|
|
Ingen indgriben: Control
Usual clinical care
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Participation in weekly phone calls
Tidsramme: 24 weeks
|
Number of weekly intervention phone calls attended or missed
|
24 weeks
|
|
Number of logins to the POWERSforID website
Tidsramme: 24 weeks
|
Number of times the POWERSforID website is accessed to journal health related behaviors
|
24 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Weight loss
Tidsramme: 24 weeks
|
Weight change measured in kilograms
|
24 weeks
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Physical activity questionnaire
Tidsramme: 24 weeks
|
The questionnaire includes assessment of perceived barriers to physical activity and physical activity participation.
|
24 weeks
|
|
Mood/Psychosocial questionnaire
Tidsramme: 24 weeks
|
Measured by the Glasgow depression scale, Psychosocial questionnaire for individuals with ID, scale for perceived physical and nutrition related barriers
|
24 weeks
|
|
Dietary recall questionnaire
Tidsramme: 24 weeks
|
The questionnaire includes assessment of type of foods consumed.
|
24 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: James Rimmer, PhD, University of Alabama at Birmingham
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. september 2016
Primær færdiggørelse (Faktiske)
1. oktober 2018
Studieafslutning (Faktiske)
1. oktober 2018
Datoer for studieregistrering
Først indsendt
22. april 2017
Først indsendt, der opfyldte QC-kriterier
3. maj 2017
Først opslået (Faktiske)
4. maj 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. november 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
13. november 2018
Sidst verificeret
1. november 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- F141230005
Plan for individuelle deltagerdata (IPD)
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