Terveellisten tapojen tekeminen kiinni (HABITS)
perjantai 26. syyskuuta 2025 päivittänyt: University of Tennessee
Terveellisten tapojen pitäminen kiinni: laajennetut kontaktitoimenpiteet afrikkalaisamerikkalaisten syövästä selviytyneiden pitkän aikavälin fyysisen toiminnan edistämiseksi
Tämän hankkeen tavoitteena on auttaa lisäämään fyysisen aktiivisuuden ylläpitoa syövästä selviytyneillä, jotka kärsivät todennäköisemmin terveyseroista ja sosiaalisista haitoista.
Tutkimuksen yleiskatsaus
Tila
Rekrytointi
Yksityiskohtainen kuvaus
Tutkimuksen tarkoituksena on arvioida uusia interventioita, jotka on suunniteltu auttamaan syövästä selviytyneitä naisia, jotka tunnistavat olevansa afrikkalaisamerikkalaisia tai mustia, voittamaan liikuntaesteitä, kehittämään fyysisesti aktiivista ajattelutapaa ja vakiinnuttamaan liikuntatottumuksia, joita tarvitaan pitkäjänteiseen harjoitteluun.
Nämä uudet interventiot ovat 1.
Tekstiviestit (SMS), 2. Vertaisvalmennus, 3. Vertaisvalmennuksen ja tekstiviestien yhdistelmä, 4. Tavallinen hoito
Opintotyyppi
Interventio
Ilmoittautuminen (Arvioitu)
260
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.
Opiskeluyhteys
- Nimi: Michelle Martin, PhD
- Puhelinnumero: 901-448-2383
- Sähköposti: mmart126@uthsc.edu
Tutki yhteystietojen varmuuskopiointi
- Nimi: Talia Williams, BA
- Puhelinnumero: 901-448-8682
- Sähköposti: twill213@uthsc.edu
Opiskelupaikat
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Alabama
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Birmingham, Alabama, Yhdysvallat, 35294
- Rekrytointi
- University of Alabama at Birmingham
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Ottaa yhteyttä:
- Laura Rogers, MD, MPH
- Puhelinnumero: 205-934-9735
- Sähköposti: lqrogers@uabmc.edu
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Ottaa yhteyttä:
- Ildiko Nyikos, MA, ACSM-RCEP, EIM-3
- Puhelinnumero: 205-975-0002
- Sähköposti: inyikos@uabmc.edu
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Päätutkija:
- Laura Rogers, MD, MPH
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Tennessee
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Memphis, Tennessee, Yhdysvallat, 38163
- Rekrytointi
- University of Tennessee Health Science Center
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Ottaa yhteyttä:
- Michelle Martin, PhD
- Puhelinnumero: 901-448-2383
- Sähköposti: mmart126@uthsc.edu
-
Ottaa yhteyttä:
- Talia Williams, BA
- Puhelinnumero: 901-448-8682
- Sähköposti: twill213@uthsc.edu
-
Päätutkija:
- Michelle Martin,, PhD
-
-
Osallistumiskriteerit
Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Ei
Kuvaus
Sisällön kriteerit:
- 19-vuotias tai vanhempi nainen
- tunnistaa olevansa afroamerikkalainen tai musta
- on ollut syöpää
- olet suorittanut syövän perushoidon jälkeisen hoidon (eli kemoterapia, sädehoito)
- suostut antamaan tutkimusryhmän vahvistaa syöpädiagnoosi lääkärisi kanssa
- Jos leikkaus on tehty, sen on oltava vähintään 8 viikkoa leikkauksen jälkeen
- halukas säännöllisen lääkärin antamaan lääketieteellisen selvityksen tutkimukseen osallistumista varten
- valmis antamaan kotiosoitteen, jos hän on pätevä tutkimukseen
- halukas ja kykenevä käyttämään videoneuvottelualustaa, kuten Zoom, opiskelutoimintoihin (on oltava sekä halukas että kykenevä)
- haluaa ja pystyy lähettämään ja/tai vastaanottamaan tekstiviestejä (on oltava sekä halukkaita että kykeneviä)
- on yhdysvaltalainen puhelinnumero
- on sähköpostiosoite
- Jos sinulla ei ole sähköpostiosoitetta, sinun on oltava valmis luomaan sellainen
- Englantia puhuva
- Pystyy liikkumaan ilman apua (ei tarvitse käyttää keppiä, kävelijää tai pyörätuolia)
- halukas ja kykenevä suorittamaan omatoimisesti 3-5 harjoitusta viikossa opiskelun ajan; jos vastasit ei, selitä
- halukas osallistumaan yksittäisiin ja ryhmäistuntoihin videokonferenssien kautta opiskelun aikana; jos vastasit ei, selitä.
- halukas osallistumaan arviointeihin videokonferenssin kautta tutkimukseen osallistumisen aikana; jos vastasit ei, selitä.
- halukas täyttämään kyselyitä tutkimukseen osallistumisen aikana; jos vastasit ei, selitä.
Poissulkemiskriteerit:
- Metastaattinen tai uusiutuva syöpä
- toinen syöpädiagnoosi viimeisen 5 vuoden aikana (ei sisällä iho- tai kohdunkaulansyöpää in situ)
- sinulla on vakava ortopedinen sairaus, nivelet tai jokin muu sairaus, joka estää henkilöä olemasta aktiivinen
- epästabiili angina pectoris
- sinulla on maalia, puristavaa tunnetta tai rasitusta rinnassa JOKO levossa TAI sitten fyysisesti aktiivisena
- joilla on New York Heart Associationin luokan II, III tai IV kongestiivinen sydämen vajaatoiminta
- verenpaine on ollut yli 160/100 vähintään kahdesti viimeisen 6 kuukauden aikana (joko numero; 160 tai 100)
- sinulla on hallitsematon astma
- sinulla on interstitiaalinen keuhkosairaus, joka vaatii ylimääräistä happea
- sinulla on dementia tai järjestäytynyt aivosyndrooma
- sinulla on skitsofrenia tai aktiivinen psykoosi
- sinulla on ollut aivohalvaus tai muu ongelma, joka on aiheuttanut vamman tai halvauksen (ei pysty liikkumaan tai tuntemaan mitään kehon osaa)
- sinulla on kuuloongelmia, jotka vaikeuttavat puhelinkeskustelun jatkamista
- sokea tai osittain sokea
- suunniteltu leikkaus tutkimukseen osallistumisen ensimmäisen kuuden kuukauden aikana (jos PI ei ole hyväksynyt)
- suunniteltu polvi- tai lonkkaleikkaus tutkimukseen osallistumisen ensimmäisen 6 kuukauden aikana
- ennakoida tavanomaisten lääkkeiden muutoksia tutkimukseen osallistumisen ensimmäisten 6 kuukauden aikana (jos PI ei ole hyväksynyt)
- lääkäri on käskenyt harjoittaa vain lääkärin määräämää liikuntaa
- lääkäri on kehottanut rajoittamaan fyysistä aktiivisuutta
- on vasta-aihe harjoittaa kohtalaisen intensiivistä aerobista harjoittelua
- olet harjoitellut keskimäärin yli 90 minuuttia/viikko kohtalaisen intensiivistä tai enemmän kuin 30 minuuttia/viikko voimakasta liikuntaa viimeisen 6 kuukauden aikana
- ongelmia tasapainon tai turvallisen liikkumisen kanssa
- ovat tällä hetkellä raskaana tai odottavat raskaana tutkimukseen osallistumisen aikana
- osallistuu parhaillaan toiseen harjoitustutkimukseen
- joiden BMI on ≥ 50
Opintosuunnitelma
Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Tukevaa hoitoa
- Jako: Satunnaistettu
- Inventiomalli: Tehtävätehtävä
- Naamiointi: Kaksinkertainen
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
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Kokeellinen: Vertaisvalmentaja ja tekstiviesti
SMS- ja vertaisvalmentajan interventiot keskittyivät liikunnan ylläpitämiseen
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Short Message System (SMS) -interventio keskittyy henkilökohtaisiin, mukautuviin tekstiviesteihin, jotka auttavat osallistujaa ylläpitämään fyysistä aktiivisuutta.
Vertaisvalmentaja antaa intervention, joka auttaa osallistujia ylläpitämään fyysistä aktiivisuutta.
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Kokeellinen: Vertaisvalmentaja
Vertaisvalmentajan interventio keskittyi liikunnan ylläpitämiseen
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Vertaisvalmentaja antaa intervention, joka auttaa osallistujia ylläpitämään fyysistä aktiivisuutta.
Muut nimet:
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Kokeellinen: Lyhytsanomapalvelu (SMS)
SMS-interventio keskittyi liikunnan ylläpitämiseen
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Short Message System (SMS) -interventio keskittyy henkilökohtaisiin, mukautuviin tekstiviesteihin, jotka auttavat osallistujaa ylläpitämään fyysistä aktiivisuutta.
Muut nimet:
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Muut: Tavallinen hoito
Fyysisen aktiivisuuden ylläpitämiseen keskittynyt kirjallinen materiaali
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Osallistujille jaetaan kirjallista materiaalia, jossa neuvotaan fyysisen aktiivisuutensa ylläpitämisessä.
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Fyysinen aktiivisuus (potilaan raportoima tulos)
Aikaikkuna: Perustasosta 15 kuukauden arvioon
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Osallistujat käyttävät liiketunnistinta vyötäröllä 7 päivän ajan
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Perustasosta 15 kuukauden arvioon
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Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Väsymys (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Väsymys mitataan Väsymysoireiden inventointi (väsymysintensiteetti ja häiriöt) -asteikolla.
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Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Itse koettu terveys (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Omaa terveyttä mitataan EQ-5D-kyselyllä.
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Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Kvalifioitu elämään (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Elämänlaatua mitataan PROMIS Global Health -kyselylomakkeella.
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Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Ahdistus ja masennus (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Ahdistuneisuutta ja masennusta mitataan sairaalan ahdistuneisuus- ja masennusasteikolla.
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Lähtötilanteessa 3 kuukauden arviointi, 9 kuukauden arviointi ja 15 kuukauden arviointi.
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Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Stressi (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta ja 15 kuukautta
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Stressiä mitataan koetun stressin asteikolla
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Lähtötilanteessa 3 kuukautta, 9 kuukautta ja 15 kuukautta
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Terveyden sosiaaliset tekijät
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Terveyden sosiaalisia tekijöitä mitataan SDoH (Social Determinants of Health) -kyselylomakkeella.
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Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Big Five -persoonallisuus (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Big Five -persoonallisuutta mitataan käyttämällä lyhyttä versiota Big Five Personality Inventory -kyselystä.
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Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Fyysinen aktiivisuus
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Aerobista ja vastusharjoitusta mitataan Godin Aerobic Strength -kyselylomakkeella.
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Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Elämänlaatu (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Elämänlaatua mitataan EQ-5D-5L-kyselyllä.
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Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Sosiaalinen tuki liikunnalle (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Liikunnan sosiaalista tukea mitataan PA:n sosiaalisen tuen kyselylomakkeella.
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Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Heijastavat, säätelevät ja refleksiiviset prosessit (potilaan raportoima tulos)
Aikaikkuna: Lähtötilanne, 3 kuukautta, 6 kuukautta, 9 kuukautta, 12 kuukautta, 15 kuukautta
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Heijastavia, sääteleviä ja refleksiivisiä prosesseja mitataan M-PAC-fyysisen aktiivisuuden kyselylomakkeella.
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Lähtötilanne, 3 kuukautta, 6 kuukautta, 9 kuukautta, 12 kuukautta, 15 kuukautta
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Havaitut harjoituksen esteet häiriöt
Aikaikkuna: Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Harjoituksen esteet mitataan Harjoittelun havaitut esteet -kyselylomakkeella.
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Lähtötilanteessa 3 kuukautta, 9 kuukautta, 15 kuukautta
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Yhteistyökumppanit ja tutkijat
Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.
Sponsori
Yhteistyökumppanit
Tutkijat
- Päätutkija: Michelle Martin, PhD, University of Tennessee
- Päätutkija: Laura Rogers, MD, MPH, University of Alabama at Birmingham
Julkaisuja ja hyödyllisiä linkkejä
Tutkimusta koskevien tietojen syöttämisestä vastaava henkilö toimittaa nämä julkaisut vapaaehtoisesti. Nämä voivat koskea mitä tahansa tutkimukseen liittyvää.
Yleiset julkaisut
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Opintojen ennätyspäivät
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IPD-jaon käyttöoikeuskriteerit
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Ei
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