Teen and Young Adult Connections for Support From Multidisciplinary Professionals & Peers
30. november 2020 opdateret af: University of Kansas Medical Center
Teen Connections for Support From Multidisciplinary Professionals & Peers
12 month study testing mobile delivery of health information and connections to professionals and peers to improve health of teen/young adult HPN users.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
This research study will test the effect of in-home/mobile HPN support delivered to teen and young adult home parenteral nutrition (HPN) patients and family members over handheld personal computers.
Effects on health status, QoL, and fatigue will be assessed over time between groups of study subjects from the ages of 13 through 30 randomized to one of two groups.
Group One (intervention group) will receive mConnect, integrated evidence-based interventions (skill-building games, restorative naps & peer support) via mobile iPad and Internet delivery plus two real-time audiovisual encrypted connections with multidisciplinary professionals and peers.
Group Two (control group) will receive healthy activity information via mobile iPad and Internet delivery plus one real-time audiovisual encrypted connection with professionals and peers.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
83
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Kansas
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Kansas City, Kansas, Forenede Stater, 66160
- University of Kansas Medical Center
-
-
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
13 år til 30 år (Barn, Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Total parenteral nutrition (TPN) patients/users and family members/caregivers (defined as those individuals involved in daily home HPN care) age 13 and older
- TPN users (also called HPN users) ages 13 through 30 must be receiving intravenous nutrition for a non-malignant short bowel disorder
- Read, write, speak English and provide informed consent
- Be able to participate in group clinic visits
Exclusion Criteria:
- Enteral nutrition dependency only
- Less than 13 years of age
- 13 through 17 years of age without parental consent
- Currently enrolled in an intervention study or HPN management program
- Severe cognitive impairment
- Disability disorders (e.g. blindness which cannot be accommodated for active participation in the group clinics
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: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Group One
Intervention
|
mConnect is the integration of evidence-based HPN interventions delivered via professionally moderated iPad visual meetings with peers, and reinforced by HPN related skill-building games (apps) and iPad music guided short naps.
|
|
Aktiv komparator: Group Two
Control
|
iPad with a data plan and one professionally moderated iPad visual meeting with peers.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Health Survey SF-12v2 (predicts future health services use).
Tidsramme: T0 (baseline data collection)
|
Physical and mental health status from each person's perspective.
7-Item Likert
|
T0 (baseline data collection)
|
|
Quality of Life (Cantril Ladder)
Tidsramme: T0 (baseline data collection)
|
Ratings of quality of life over time that are sensitive to changes in health.
3-Item Likert
|
T0 (baseline data collection)
|
|
Beck Depression Inventory-II (BDI-II)
Tidsramme: T0 (baseline data collection)
|
Assesses assess the intensity of depression into alignment with DSM-IV criteria.
Each item is a list of four statements arranged in increasing severity about a particular symptom of depression.
21-Item
|
T0 (baseline data collection)
|
|
Use of Healthy Living Activities Prompts, health intentions that predict engagement in targeted activities.
Tidsramme: T2 (month 1-2/mConnect intervention period)
|
Intention scale for healthy activities use (iPad discussion sessions, website use including games; mConnect use) 10-Item Likert
|
T2 (month 1-2/mConnect intervention period)
|
|
Use of Healthy Living Activities Prompts, health intentions that predict engagement in targeted activities.
Tidsramme: T3 (month 3-4/mConnect intervention period)
|
Intention scale for healthy activities use (iPad discussion sessions, website use including games; mConnect use) 10-Item Likert
|
T3 (month 3-4/mConnect intervention period)
|
|
Beck Depression Inventory-II (BDI-II)
Tidsramme: T3 (4 months: change from T0/baseline)
|
Assesses assess the intensity of depression into alignment with DSM-IV criteria.
Each item is a list of four statements arranged in increasing severity about a particular symptom of depression.
21-Item
|
T3 (4 months: change from T0/baseline)
|
|
Health Survey SF-12v2 (predicts future health services use).
Tidsramme: T3 (4 months: change from T0/baseline)
|
Physical and mental health status from each person's perspective.
7-Item Likert
|
T3 (4 months: change from T0/baseline)
|
|
Quality of Life (Cantril Ladder)
Tidsramme: T3 (4 months: change from T0/baseline)
|
Ratings of quality of life over time that are sensitive to changes in health.
3-Item Likert
|
T3 (4 months: change from T0/baseline)
|
|
Health Survey SF-12v2 (predicts future health services use).
Tidsramme: T4 (8 months: change from T3/4 months)
|
Physical and mental health status from each person's perspective.
7-Item Likert
|
T4 (8 months: change from T3/4 months)
|
|
Quality of Life (Cantril Ladder)
Tidsramme: T4 (8 months: change from T3/4 months)
|
Ratings of quality of life over time that are sensitive to changes in health.
3-Item Likert
|
T4 (8 months: change from T3/4 months)
|
|
Beck Depression Inventory-II (BDI-II)
Tidsramme: T4 (8 months: change from T3/4 months)
|
Assesses assess the intensity of depression into alignment with DSM-IV criteria.
Each item is a list of four statements arranged in increasing severity about a particular symptom of depression.
21-Item
|
T4 (8 months: change from T3/4 months)
|
|
Health Survey SF-12v2 (predicts future health services use).
Tidsramme: T5 (12 months: change from T4/8 months)
|
Physical and mental health status from each person's perspective.
7-Item Likert
|
T5 (12 months: change from T4/8 months)
|
|
Quality of Life (Cantril Ladder)
Tidsramme: T5 (12 months: change from T4/8 months)
|
Ratings of quality of life over time that are sensitive to changes in health.
3-Item Likert
|
T5 (12 months: change from T4/8 months)
|
|
Beck Depression Inventory-II (BDI-II)
Tidsramme: T5 (12 months: change from T4/8 months)
|
Assesses assess the intensity of depression into alignment with DSM-IV criteria.
Each item is a list of four statements arranged in increasing severity about a particular symptom of depression.
21-Item
|
T5 (12 months: change from T4/8 months)
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Preparedness (measures skills needed for independent HPN home care).
Tidsramme: T0 (baseline data collection)
|
Ability to manage home-care; low score = needs home care assistance.
8-Item Likert
|
T0 (baseline data collection)
|
|
COOPS Social Support Scale
Tidsramme: T0 (baseline data collection)
|
Ratings on having others who help, listen & provide tangible assistance support.
13-Item Likert
|
T0 (baseline data collection)
|
|
Preparedness (measures skills needed for independent HPN home care).
Tidsramme: T3 (4 months: change from T0/baseline)
|
Ability to manage home-care; low score = needs home care assistance.
8-Item Likert
|
T3 (4 months: change from T0/baseline)
|
|
COOPS Social Support Scale
Tidsramme: T3 (4 months: change from T0/baseline)
|
Ratings on having others who help, listen & provide tangible assistance support.
13-Item Likert
|
T3 (4 months: change from T0/baseline)
|
|
Mobile Care Helpfulness & Willingness-to-Pay Fees for Distance Health.
Tidsramme: T4 (8 months)
|
Rating of Helpfulness and willingness to pay for mobile care delivery.
10-Item Likert
|
T4 (8 months)
|
|
Preparedness (measures skills needed for independent HPN home care).
Tidsramme: T4 (8 months: change from T3/4 months)
|
Ability to manage home-care; low score = needs home care assistance.
8-Item Likert
|
T4 (8 months: change from T3/4 months)
|
|
COOPS Social Support Scale
Tidsramme: T4 (8 months: change from T3/4 months)
|
Ratings on having others who help, listen & provide tangible assistance support.
13-Item Likert
|
T4 (8 months: change from T3/4 months)
|
|
Preparedness (measures skills needed for independent HPN home care).
Tidsramme: T5 (12 months: change from T4/8 months)
|
Ability to manage home-care; low score = needs home care assistance.
8-Item Likert
|
T5 (12 months: change from T4/8 months)
|
|
COOPS Social Support Scale
Tidsramme: T5 (12 months: change from T4/8 months)
|
Ratings on having others who help, listen & provide tangible assistance support.
13-Item Likert
|
T5 (12 months: change from T4/8 months)
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Carol E Smith, RN, PhD, FAAN, University of Kansas Medical Center
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
1. juli 2016
Primær færdiggørelse (Faktiske)
1. december 2019
Studieafslutning (Faktiske)
1. juni 2020
Datoer for studieregistrering
Først indsendt
6. december 2016
Først indsendt, der opfyldte QC-kriterier
8. december 2016
Først opslået (Skøn)
9. december 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
2. december 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
30. november 2020
Sidst verificeret
1. november 2020
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- STUDY00004067
- R01NR015743-01A1 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
All data is de-identified and will be reported only in aggregate.
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 .