The COACH Project: Combined Online Assistance for Caregiver Health (COACH)
Combined Online Assistance for Caregiver Health (COACH): The Efficacy of a Combined Physical Activity and Coping Skills Training Intervention for Caregivers
Studieöversikt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Studietyp
Studietyp
Inskrivning (Förväntat)
Inskrivning
Fas
Fas
- Inte tillämpbar
Kontakter och platser
Studiekontakt
Studiekontakt
- Namn: Jennifer Fairchild, PhD
- Telefonnummer: 63432 650-493-5000
Studera Kontakt Backup
- Namn: Marisol Hernandez
- Telefonnummer: 65992 650-493-5000
Studieorter
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California
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Palo Alto, California, Förenta staterna, 94304
- Rekrytering
- VA Palo Alto Health Care System
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Kontakt:
- Amerah Hashmi
- Telefonnummer: 65992 650-493-5000
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Huvudutredare:
- Jennifer K Fairchild, PhD
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-
Deltagandekriterier
Urvalskriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- individuals aged 18 - 85
- distress associated with being the primary caregiver of a person with TBI or dementia
- endorsement of at least two of the following items: felt overwhelmed, felt like needed to cry, angry or frustrated, distant or cut of from family or friends, moderate to high levels of stress, felt their health had declined
- provide at least one hour of care (supervision or direct assistance) per week over the past three months
- approval by Primary Care Provider to participate in physical exercise
- be proficient in spoken and written English
Exclusion Criteria:
- current or lifetime history of any psychiatric disorder with psychotic features
- prominent suicidal or homicidal ideation
- current alcohol or substance abuse
- diagnosis of probable or possible dementia
- a Short Portable Mental Status score of ≥ 8
- participation in another caregiver intervention within the past year
- lack of regular access to the internet
- planned transfer of care recipient to another caregiver or nursing home within 12 months; 8) current severe cardiac disease (e.g., uncontrolled atrial fibrillation, defined as mean 24 hour heart rate >85 beats/min, or 24 hour maximal ventricular rate >150 beats/min; uncontrolled ventricular arrhythmias, defined as recurrent ventricular tachycardia >3 beats in succession, or 24 hour PVC count >20%; active pericarditis or myocarditis; Class III/IV heart failure and / or ejection fraction < 20%; thrombophlebitis; pulmonary disease with a drop in O2 Sat with exercise to 90% without oxygen; embolism within past 6 months)
- inability to participate in an exercise stress test
- morbid obesity (BMI > 39)
- inability to read, verbalize understanding and voluntarily sign the Informed Consent.
Caregivers meeting any of these exclusion criteria will be excluded from all aspects of this project.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Antal vapen
Vapen och interventioner
Deltagargrupp / ArmDeltagargrupp / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Experimentell: Combined Aerobic and Resistance Exercise
Participants will work with study staff to develop an individualized physical training program based on their level of functioning at study entry.
Exercises will focus on increasing the heart rate to a point at which participants will breathe more heavily and may sweat.
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The combined moderate to high intensity combined aerobic and resistance exercise training + skills training group consists of six months of physical exercise + caregiver skills training followed by an additional six months of follow-up for a total study duration of twelve months.
All aspects of these combined interventions will be delivered through mobile technology thus obviating some of the obstacles to caregivers face in meeting their own needs.
Caregivers will be provided with study issued equipment (e.g., exercise equipment, activity monitoring devices, and tablets) to complete all elements of the intervention.
|
|
Aktiv komparator: Balance and Flexibility
Participants will work with study staff to develop an individualized physical training program based on their level of functioning at study entry.
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The stretching, balance and flexibility training + skills training group consists of six months of physical exercise + caregiver skills training followed by an additional six months of follow-up for a total study duration of twelve months.
All aspects of these combined interventions will be delivered through mobile technology thus obviating some of the obstacles to caregivers face in meeting their own needs.
Caregivers will be provided with study issued equipment (e.g., exercise equipment, activity monitoring devices, and tablets) to complete all elements of the intervention.
|
Vad mäter studien?
Primära resultatmått
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Caregiver Burden using Zarit Burden Inventory
Tidsram: Six Months
|
Zarit Burden Inventory
|
Six Months
|
Samarbetspartners och utredare
Sponsor
Sponsor
Samarbetspartners
Samarbetspartners
Studieavstämningsdatum
Studera stora datum
Studiestart
Studiestart
Primärt slutförande (Förväntat)
Primärt slutförande
Avslutad studie (Förväntat)
Avslutad studie
Studieregistreringsdatum
Först inskickad
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Första postat
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste uppdatering publicerad
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Mentala störningar
- Hjärnsjukdomar
- Sjukdomar i centrala nervsystemet
- Sjukdomar i nervsystemet
- Sår och skador
- Neurokognitiva störningar
- Neurodegenerativa sjukdomar
- Trauma, nervsystemet
- Tauopatier
- Huvudskador, stängt
- Sår, Icke-penetrerande
- Hjärnskador
- Demens
- Hjärnskador, traumatiska
- Alzheimers sjukdom
- Kraniocerebralt trauma
- Hjärnskakning
Andra studie-ID-nummer
Andra studie-ID-nummer
- FAI0003AGG
- W81XWH-15-1-0246 (Annat bidrag/finansieringsnummer: Department of Defense)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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