- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03002896
Mobilized Psychoeducation and Skills Based Intervention (Pep-Pal) for Caregivers of Patients With Advanced Illness
31 juli 2020 uppdaterad av: University of Colorado, Denver
A Pilot Study of a Mobilized Psychoeducation and Skills Based Intervention (Pep-Pal) for Caregivers of Patients With Advanced Illness
The proposed project is a pilot study of the Pep-Pal (Psychoeducation and Skills Based Intervention) versus a treatment as usual control group.
A total of 60 caregivers; including caregivers of patients with HSCT (Hematopoietic Stem Cell Transplantation), caregivers enrolled in Phase I clinical trials, and caregivers of patients with advanced cancer (Stage III, solid tumor) will be enrolled in this study.
The investigators do not expect different outcomes from these three groups, rather these populations are selected to optimize recruitment within a short time frame.
The caregivers will be randomized to either treatment as usual or Pep-Pal intervention.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
The proposed project is a pilot study of the Pep-Pal intervention versus a treatment as usual control group.
A total of 60 caregivers; caregivers of patients with HSCT, caregivers of patients enrolled in phase I oncology trials, and caregivers of patients with advanced cancer (Stage IV, solid tumor) will be enrolled in this study.
The investigators do not expect different outcomes from these three groups, rather these populations are selected to optimize recruitment within a short time frame.
The caregivers will be randomized to either treatment as usual or Pep-Pal intervention.
The proposed study population is based on prior research indicating that caregivers of patients receiving HSCT, caregivers of patients enrolled in phase I oncology trials, and caregivers of patients with advanced cancer experience significant distress.
In addition, an initial study of caregivers of patients receiving allogeneic-HSCT were able to benefit from a brief, cognitive behavioral stress management treatment approach.
A study examining distress in phase I oncology clinical trial patient caregivers highlighted the need for more support for this significantly distressed population.
Furthermore, initial results of the qualitative development study for Pep-Pal yielded support for a mobilized platform delivery of resources for caregivers to manage distress because they acknowledged many barriers to engaging in in-person treatment to manage distress.
Studietyp
Interventionell
Inskrivning (Faktisk)
69
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Colorado
-
Aurora, Colorado, Förenta staterna, 80045
- University of Colorado, Denver
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 85 år (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Women and men ≥ 18 years of age of any ethnicity
- Must endorse a moderate level of anxiety (e.g. Score above an 8 on the Hospital and Anxiety Depression Scale (HADS))
- Speak and read in English
- Caregiver of a patient with auto HSCT who are moving forward with bone marrow transplant or have receive a bone marrow transplant
- Caregiver of a patient in a Phase I Clinical Trial
- Caregiver of a patient diagnosed with advanced cancer (stage III or stage IV)
- No Cognitive or psychiatric conditions prohibiting participation
- Must meet criteria for being a primary caregiver, defined as, the person in the patient's life who is primarily responsible for care decisions, emotionally invested in the patient's care, provides instrumental care such as transportation for a patient receiving auto-HSCT, enrolled in a phase I oncology clinical trial, or of a patient diagnosed with advanced cancer (stage IV, solid tumor).
- Have a computer, smartphone, or tablet with internet access
Exclusion Criteria:
- Caregivers below the age of 18
- Score below an 8 on the Hospital and Anxiety Depression Scale (HADS)
- Cannot speak and read in English
- Patient does not receive a bone marrow transplant
- Patient is not enrolled in a Phase I clinical trial
- Patient is not diagnosed with Stage III or Stage IV cancer
- Cognitive conditions prohibiting participation
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Stödjande vård
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: Pep-Pal + Treatment as Usual
If the caregiver is assigned to the Pep-Pal intervention condition, the RA will provide access to the mobilized website (passcode) through an email.
Caregivers will be instructed to watch each session at least once.
It will be recommended that caregivers watch one to two new sessions per week so that they can have enough time to practice the skills between sessions.
In addition, they will be told that they can go back and watch the sessions for review as many times as they like.
Full participation will be defined as watching at least 7/9 sessions (75% of program) based on previous criteria for similar intervention completion in a prior trial with advanced cancer patients.
|
Pep-Pal is designed to complement the utilization of other resources, provide support when no other resources can be obtained, or provide support in the interim until greater resources can be obtained.
In this way, Pep-Pal is a resource for our most hard to reach caregivers.
|
Aktiv komparator: Treatment as Usual
Treatment as usual provides voluntary (at the caregiver's discretion) support services for the caregivers which is rarely used by the caregivers.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Evaluation of Exit Interviews
Tidsram: 12 weeks
|
Qualitative feedback will be gathered from the first 15 Pep-Pal completer's for individual interviews (5 from Phase I group, 5 from Hematopoietic stem cell transplantation (HSCT) group, 5 from medical oncology) upon completion of the follow-up assessments at 12 weeks about usage, acceptability of content, and impressions of using Pep-Pal.
|
12 weeks
|
Pep-Pal Self-Report sessions at 12 Weeks
Tidsram: 12 weeks
|
The Investigators will assess feasibility by examining recruitment, retention, as well as reasons for refusal, frequency of sessions watched and length of time spent watching each session.
Self report usage of peppal: Usage of Pep-Pal will be quantitatively assessed by asking each participant in the intervention group about their usage including frequency; how many times they watched each session and length of viewing for each session (partial or complete).
They will be asked to rate level of usage based on a Likert-scale ranging from not at all to very often for each session (0-10).
They will be asked to rank order the list of sessions from most helpful to least helpful.
|
12 weeks
|
Evaluation of Self-Report Caregiver reported outcomes at Baseline
Tidsram: Week 1
|
Hospital Anxiety and Depression Scale-Anxiety subscale (HADS-A)
|
Week 1
|
Evaluation of Self-report caregiver reported outcomes at 12 weeks
Tidsram: Week 12
|
Hospital Anxiety and Depression Scale-Anxiety subscale (HADS-A)
|
Week 12
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Evaluation of Self-report caregiver reported outcomes at baseline
Tidsram: Week 1
|
Center for Epidemiologic Studies Depression Scale (CESD)
|
Week 1
|
Evaluation of Self-report caregiver reported outcomes at baseline
Tidsram: Week 1
|
Perceived Stress Scale (PSS)
|
Week 1
|
Evaluation of Self-report caregiver reported outcomes at baseline
Tidsram: Week 1
|
Female Sexual Function Index (FSFI)
|
Week 1
|
Evaluation of Self-report caregiver reported outcomes at baseline
Tidsram: Week 1
|
Male Sexual Health Questionnaire(MSHQ)
|
Week 1
|
Evaluation of Self-report caregiver reported outcomes at baseline
Tidsram: Week 1
|
Measure of Current Status (MOCS-A)
|
Week 1
|
Evaluation of Self-report caregiver reported outcomes at 12 weeks
Tidsram: Week 12
|
Center for Epidemiologic Studies Depression Scale (CESD)
|
Week 12
|
Evaluation of Self-report caregiver reported outcomes at 12 weeks
Tidsram: Week 12
|
Perceived Stress Scale (PSS)
|
Week 12
|
Evaluation of Self-report caregiver reported outcomes at 12 weeks
Tidsram: Week 12
|
Female Sexual Function Index (FSFI)
|
Week 12
|
Evaluation of Self-report caregiver reported outcomes at 12 weeks
Tidsram: Week 12
|
Male Sexual Health Questionnaire(MSHQ)
|
Week 12
|
Evaluation of Self-report caregiver reported outcomes at 12 weeks
Tidsram: Week 12
|
Measure of Current Status (MOCS-A)
|
Week 12
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Nicole R Amoyal-Pensak, PhD, University of Colorado, Denver
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- Pensak NA, Carr AL, Jones J, Mikulich-Gilbertson SK, Kutner JS, Kilbourn K, Sannes TS, Brewer BB, Kolva E, Joshi T, Laudenslager ML. A pilot study of mobilized intervention to help caregivers of oncology patients manage distress. Psychooncology. 2021 Apr;30(4):520-528. doi: 10.1002/pon.5597. Epub 2020 Dec 2.
- Carr AL, Jones J, Mikulich Gilbertson S, Laudenslager ML, Kutner JS, Kilbourn K, Sannes TS, Brewer BW, Kolva E, Joshi T, Amoyal Pensak N. Impact of a Mobilized Stress Management Program (Pep-Pal) for Caregivers of Oncology Patients: Mixed-Methods Study. JMIR Cancer. 2019 May 3;5(1):e11406. doi: 10.2196/11406.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
1 december 2016
Primärt slutförande (Faktisk)
17 november 2017
Avslutad studie (Faktisk)
13 juli 2018
Studieregistreringsdatum
Först inskickad
28 september 2016
Först inskickad som uppfyllde QC-kriterierna
21 december 2016
Första postat (Uppskatta)
26 december 2016
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
4 augusti 2020
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
31 juli 2020
Senast verifierad
1 juli 2020
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 16-0990
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
Kliniska prövningar på Depression
-
ProgenaBiomeRekryteringDepression | Depression, postpartum | Depression, ångest | Depression Måttlig | Depression Svår | Klinisk depression | Depression i remission | Depression, Endogen | Depression KroniskFörenta staterna
-
Kintsugi Mindful Wellness, Inc.Sonar Strategies; Vituity PsychiatryRekryteringDepression | Depression Måttlig | Depression Svår | Depression MildFörenta staterna
-
University of California, San FranciscoRekryteringDepression Måttlig | Depression Mild | Depression, tonåringFörenta staterna
-
University GhentUniversiteit Antwerpen; Janssen-Cilag Ltd.Rekrytering
-
Washington University School of MedicineAvslutadBehandling Resistent depression | Senlivsdepression | Geriatrisk depression | Refraktär depression | Terapiresistent depressionFörenta staterna, Kanada
-
Baylor College of MedicineUniversity of TexasRekryteringDepression | Depression Måttlig | Depression Svår | Självmord och självskada | Depression i tonåren | Depression MildFörenta staterna
-
University of Cape TownNational Institute of Mental Health (NIMH)AvslutadPostpartum depression | Klinisk depression | Måttlig depressionSydafrika
-
Northern Illinois UniversityUniversity Autonoma de Santo DomingoAvslutadDepression Måttlig | Depression MildFörenta staterna, Dominikanska republiken
-
Gerbera Therapeutics, Inc.Har inte rekryterat ännuPostpartum depression | Depression, postpartum | Postnatal depression | Post-partum depression | Post-Natal depressionFörenta staterna
-
Federal Research Center of Fundamental and Translational...AvslutadDepression Måttlig | Depression MildRyska Federationen
Kliniska prövningar på Behandling som vanligt
-
Oui Therapeutics, Inc.National Institute of Mental Health (NIMH)Har inte rekryterat ännuSjälvmordstankar
-
Duke UniversityNational Institute of Nursing Research (NINR); Palliative Care Research...Avslutad
-
Wake Forest University Health SciencesDuke University; University of RochesterAvslutadSjälvmord | Föräldraskap | Självförmåga | Ångest; ModerligFörenta staterna
-
Hôpital le VinatierNantes University Hospital; Centre Hospitalier Henri Laborit; University... och andra samarbetspartnersAvslutadKronisk schizofreniFrankrike
-
Brown UniversityNational Institute of Mental Health (NIMH)RekryteringHIV/AIDSFörenta staterna
-
The University of Texas Health Science Center at...AvslutadKronisk smärtaFörenta staterna
-
Ioannis A. MalogiannisNational and Kapodistrian University of Athens; Attikon Hospital; University... och andra samarbetspartnersRekrytering
-
International Rescue CommitteeJohns Hopkins University; World Health OrganizationAvslutad
-
Case Western Reserve UniversityAvslutadBipolär sjukdomFörenta staterna
-
University of MichiganNational Institute of Mental Health (NIMH)RekryteringPosttraumatisk stressyndromFörenta staterna