Habit Formation in Older Adults: Feasibility Study
Forming New Habits: A Feasibility Study on an Intervention to Decrease Sedentary Behaviors in Medically Stable Older Adults
Sedentary behavior, which is characterized by too much sitting, is an epidemic in the United States. It is estimated that 4 out of every 10 Americans never engage in physical activity, and approximately 60% of an adult's non-sleeping hours are spent in sedentary behaviors. This equates to approximately 9-10 hours per day. As sedentary behavior increases, so do diagnoses of chronic illnesses such as diabetes, hypertension, cardiovascular disease, and kidney disease. Older adults are particularly at risk for sedentary behavior and the related chronic illnesses.
The primary aim of this study is to investigate the feasibility of implementing the EMA intervention with medically stable older adults who are living in the community.
The secondary aims of this study are to investigate the effectiveness of the Everyday Meaningful Activities (EMA) Intervention in forming active lifestyle behavior habits and in decreasing an individual's perceived sedentary time.
This prospective study will examine the ability of medically stable older adults to decrease sedentary behavior by creating new, active lifestyle behavior habits using the Everyday Meaningful Activities intervention. The EMA Intervention is based in Habit Formation Theory. It is an individualized, client-centered intervention that aims to increase adherence to active lifestyle behaviors in older adults' lives. Participants will engage in the EMA Intervention that is designed to create new active lifestyle behavior habits by attaching these new active lifestyle behaviors to currently existing daily routines.
During six intervention sessions over six weeks, participants will select two new active lifestyle behaviors to make habitual and will create action plans to create the habits. The first behavior will be implemented at the first intervention session, and the second behavior will be implemented at the fourth session. The participants will be assessed three times over their 8 to 10-week study participation. Participants should (1) be 65 years of age and older, (2) have intact cognition, (3) have no self-reported physical activity limitations, (4) have a sedentary lifestyle, and (5) have no acute illnesses or unstable medical conditions.
The results of this study may provide evidence for the occupational therapy intervention to decrease sedentary behavior in older adults in the community. The results may also broaden the scope of occupational therapy practice through demonstrating the potential for occupational therapy services in preventive health care.
Tutkimuksen yleiskatsaus
Tila
Ehdot
Interventio / Hoito
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Opiskelupaikat
-
-
North Carolina
-
Greenville, North Carolina, Yhdysvallat, 57834
- East Carolina University
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- age 65 or older,
- intact cognition as confirmed by the Montreal Cognitive Assessment blind version
- no physical activity restrictions that can be self-reported
- sedentary lifestyle as confirmed by the Rapid Assessment Disuse Index
- live within 20 miles of the College of Allied Health Sciences at ECU
- have access to the internet and/or a telephone for remote intervention sessions
Exclusion Criteria:
- acute or terminal illness
- myocardial infarction in the previous 6 months
- unstable cardiovascular disease
- unstable metabolic disease
- neuromusculoskeletal disorders that severely impact voluntary movement
- limb amputation
- upper or lower extremity fracture in the previous 3 months
- current symptomatic hernia
- current symptomatic hemorrhoids
- cognitive impairment
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Ei käytössä
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Ei mitään (avoin tarra)
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Recruitment rate
Aikaikkuna: Through study completion, an average of 1 year
|
The recruitment rate for medically stable older adults in the community for this study
|
Through study completion, an average of 1 year
|
|
Appropriateness of the Rapid Assessment Disuse Index (RADI)
Aikaikkuna: During screening
|
The appropriateness of the Rapid Assessment Disuse Index (RADI) for screening sedentary behavior in older adults over the phone
|
During screening
|
|
Appropriateness of the Short Blessed Test
Aikaikkuna: During screening
|
the appropriateness of the Short Blessed Test for screening sufficient cognitive ability in older adults over the phone
|
During screening
|
|
Appropriateness of video conferencing through WebEx on an iPad
Aikaikkuna: For 6 weeks
|
The appropriateness of video conferencing through WebEx on an iPad as an acceptable delivery method of selected intervention sessions
|
For 6 weeks
|
|
Reliability of participants' subjective reports
Aikaikkuna: For 6 weeks
|
The reliability of participants' subjective reports of exact times for performing active lifestyle behaviors
|
For 6 weeks
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Changes in the Self-Report Habit Index
Aikaikkuna: 1) intervention session 1 at Week 1; 2) intervention session 4 at Week 4, and 3) posttest at Week 7
|
The Self-Report Habit Index (SRHI) measures features of habits including repetition, automaticity, and expressing identity.
This 12-item assessment assesses the strength of habits by differentiating habit strength from behavior frequency.
The participants will choose two active lifestyle behaviors to incorporate into their daily lives.
The SRHI will generate pretest and posttest data for each behavior.
The items in the SRHI began with the stem "Behavior X is something…" and is then followed by 12 statements rated on a scale from 1 (very strongly agree) to 7 (very strongly disagree).
A total score ranges from 1 to 84 with lower scores indicating stronger habits.
|
1) intervention session 1 at Week 1; 2) intervention session 4 at Week 4, and 3) posttest at Week 7
|
|
Changes in Sedentary Behavior Questionnaire
Aikaikkuna: 1) intervention session 1 at Week 1, and 2) posttest at Week 7
|
The Sedentary Behavior Questionnaire (SBQ) is a self-report questionnaire about time spent in sedentary behaviors both on weekdays and weekends.
There are 9 identical items on the weekday form and the weekend form.
Participants will complete both forms at both time points.
The SBQ is used to assess the participants' perceived sedentary time.
A total score ranges from 0 to 54 for each (weekday and weekend), with higher scores indicating more sedentary behaviors.
|
1) intervention session 1 at Week 1, and 2) posttest at Week 7
|
Yhteistyökumppanit ja tutkijat
Sponsori
Tutkijat
- Päätutkija: Young Joo Kim, PhD, East Carolina University
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muut tutkimustunnusnumerot
- UMCIRB 19-001365
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .
Kliiniset tutkimukset Vanhemmat aikuiset
-
Cedars-Sinai Medical CenterHuntington Hospital; UniHealth Foundation; Ronald Reagan Medical Center; Torrance...ValmisFrail Older Adutls
-
Aalborg UniversityAalborg Municipality; Imasen Electrical Industrial Co., Ltd.ValmisPre-frail Senior AdultsTanska
Kliiniset tutkimukset Everyday Meaningful Activities (EMA) intervention
-
The University of Hong KongHealth and Medical Research FundValmisTupakoinnin lopettaminenHong Kong
-
Chestnut Health SystemsNational Institute on Drug Abuse (NIDA)ValmisElpyminen | Päihteiden käyttöhäiriö (SUD)Yhdysvallat
-
The University of Hong KongResearch Grants Council, Hong KongValmis
-
The University of Hong KongThe Hong Kong Jockey Club Charities TrustIlmoittautuminen kutsustaYlipaino tai liikalihavuus | Terveellinen dieetti | Painon muutos | Kehon rasvaa | Fyysiset aktiviteetit | LihasmassaHong Kong
-
Ilona MyllyniemiUniversity of CambridgeEi vielä rekrytointiaAlkoholin juominen | Alkoholiriippuvuus | Alkoholin käytön häiriö | Alkoholin väärinkäyttö | Alkoholimyrkytys
-
Rutgers, The State University of New JerseyRekrytointiItsemurha-ajattelu | Itsemurha | ItsemurhayritysYhdysvallat
-
Massachusetts General HospitalRutgers UniversityValmisItsemurha-ajattelu | ItsemurhayritysYhdysvallat