- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02596672
Promoting Walking in Older Adults Living in Independent Living Communities in Northern Ireland: A Feasibility Study.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
-
Belfast, Det Forenede Kongerige, BT12 6BJ
- Centre for Public Health, Queen's University Belfast
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Adults over the age of 60 years recruited from fold housing associations, dependent on site; those receiving nursing care will not be included.
- Inactive/not regularly walking (less than 30 minutes
- Have the ability to read, write, understand and speak English.
- Can walk freely without human assistance (residents will be included they use a walking stick/walking aid.)
Exclusion Criteria:
- If they have fallen in the last 6 months
- Have regular nursing assistance/care within the fold
- Residents with dementia or other cognitive challenges will be excluded.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Intervention
They will complete a 12-week peer-led walking programme.
Participants will be paired together as walking partners and will be given a pedometer and step count logs for self-monitoring.
The walking co-ordinators will facilitate walking groups two times a week in the local areas, lasting for 30 minutes.
The nature of the walks will be tailored to the participants stated preferences of types of activity.
Participants will also receive local walking route maps.
After 12 weeks, the formal peer-led component will finish and participants will be encouraged to continue walking with their walking partners other activity programmes organised in the fold in order to maintain activity levels.
|
A 12 week peer led walking group for adults and older adults (> 55 years) living in independent living communities in Northern Ireland.
Designed to increase physical activity levels of inactive older adults and measure sustained changes in physical behaviour 6 months after the intervention ends.
|
|
Ingen indgriben: Control
Folds assigned to the control group will not receive any additional support to change their physical activity behaviour over the course of the intervention period. At the six-month data collection point they will be offered a referral to a local walking group in their area or advice on beginning a self-directed walking programme (similar to Public Health Agency www.choosetolivebetter.com/content/getting-active). They will be asked to complete outcome measures at baseline and follow up time-points. Post-study a sample of control participants will be asked to attend a focus group, exploring their views on social activity as form of physical activity for older adults in folds. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Moderate-to-vigorous physical activity (MVPA)
Tidsramme: Baseline, 12 weeks and 6 months
|
Changes from baseline MVPA as assessed by Actigraph accelerometer
|
Baseline, 12 weeks and 6 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Quality of Life
Tidsramme: Baseline, 12 weeks and 6 months
|
To explore changes in health-related quality of life, a validated self-reported questionnaire EuroQol-5D will be completed by study participants.
|
Baseline, 12 weeks and 6 months
|
|
Self-efficacy
Tidsramme: Baseline, 12 weeks and 6 months
|
Changes in self-efficacy will be measured using a short version of exercise behaviour self-confidence questionnaire.
|
Baseline, 12 weeks and 6 months
|
|
Physical and Mental Health
Tidsramme: Baseline, 12 weeks and 6 months
|
Changes in other health-related and well-being outcomes will include completing the (7 item) Warwick-Edinburgh Mental Well-being score.
|
Baseline, 12 weeks and 6 months
|
|
Social Engagement
Tidsramme: Baseline, 12 weeks and 6 months
|
Changes in social engagement will be measured using the Lubben social network scale
|
Baseline, 12 weeks and 6 months
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Mark A Tully, PhD, Queen's University, Belfast
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 15.30
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Fysisk aktivitet
-
NYU Langone HealthAfsluttetAttention Deficit Hyper ActivityForenede Stater
-
Texas Woman's UniversityAfsluttetIntellektuel handicap | Autismespektrumforstyrrelse | Motoriske lidelser | Motorforsinkelse | Sanseforstyrrelser | Attention Deficit Hyper Activity
-
University of ValenciaAfsluttetAutismespektrumforstyrrelse | Attention Deficit Hyper ActivitySpanien
-
Cingulate TherapeuticsPremier Research Group plcAfsluttetADHD | Attention Deficit Hyperactivity Disorder | ADHD - kombineret type | Attention Deficit Hyperactivity Disorder kombineret | Attention Deficit Hyper Activity | Opmærksomhedsunderskud hyperaktivitetForenede Stater
-
Cingulate TherapeuticsSuspenderetADHD | Attention Deficit Hyperactivity Disorder | Attention Deficit Disorder med hyperaktivitet | ADHD - kombineret type | Attention Deficit Hyperactivity Disorder kombineret | Attention Deficit Hyper Activity | Opmærksomhedsunderskud hyperaktivitetForenede Stater
-
Affiliated Hospital to Academy of Military Medical...Cancer Institute and Hospital, Chinese Academy of Medical Sciences; Peking...RekrutteringAldersinterval ≥16 år, køn ubegrænset | Histopatologi bekræftet diffust stort B-celle lymfom eller højgradigt B-celle lymfom | Modtaget tidligere førstelinjekemoterapi for DLBCL eller HGBL, kunne ikke nå CR i fire cyklusser eller tilbagefald | Mindst én positiv læsion ifølge 2014 Lugano-kriterierne... og andre forholdKina
Kliniske forsøg med The friendly walking group
-
Fondazione IRCCS Istituto Nazionale dei Tumori,...Afsluttet
-
University of ValenciaAfsluttetCoronavirusinfektion | LuftvejssygdomSpanien
-
The University of Hong KongHong Chi AssociationAfsluttetIntellektuel handicap | Mor-barn forholdHong Kong
-
Children's Hospital Los AngelesAmerican Psychological FoundationRekruttering
-
Yi LiangZhejiang Provincial Department of Science and TechnologyIkke rekrutterer endnuKronisk atrofisk gastritisKina
-
Dokuz Eylul UniversityAfsluttet
-
Children's Hospital of PhiladelphiaNational Institutes of Health (NIH); National Center for Complementary...Afsluttet