- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01912157
Couples Coping With Multiple Chronic Medical Conditions (GUGKS)
Couples Coping With Multimorbidity: Does Solitary Expressive Writing Foster Psycho-social Adaptation?
Handling of complex health situations (as defined by multimorbidity) in partnership: communication between romantic partners; subjective illness perception; coping with stressful experiences due to multimorbidity.
Intervention : Expressive Writing about subjective illness perception vs. Writing about individual Time-Management Primary Endpoint: subjective Health (e.g. SF 12 questionnaire) Secondary Endpoints: Psychosocial Adjustments (Depression, somatic symptoms, quality of partnership and others)
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Coping in complex health situations (as defined by multimorbidity) and the role of relationship processes for psycho-social adaption: The study investigates interpersonal emotion regulation, disclosure, and illness perceptions in couples with a multimorbid patient. The intervention consists in 3 self-applied solitary written disclosure sessions (expressive writing), the control condition are 3 sessions writing about individual time-management (placebo).
Primary endpoint: subjective health (SF 12 questionnaire) Secondary endpoint: psychosocial adjustments (depression, positive and negative affect, somatic symptoms, adjustment disorder, marital satisfaction, sleep quality)
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
ZH
-
Zurich, ZH, Schweiz, 8091
- University Hospital Zurich, Internal Medicine
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion criteria:
- Age 18 or older
- multimorbid condition (two or more chronic medical conditions)
- patients living with romantic partner
- very good oral and written command in German
- written consent for participation by patient and partner
Exclusion criteria:
- Pregnancy
- Mini Mental State less than 26
- Substance Abuse
- Patients in Palliative Situation
- Patients isolated due to infectious diseases
- Patients participating in other clinical trials within the last 4 weeks before inclusion
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Placebo komparator: No Intervention
The control condition are 3 sessions writing about individual time-management (placebo).
|
The intervention consists in 3 self-applied solitary written disclosure sessions (expressive writing)
|
|
Aktiv komparator: Expressive Writing
The intervention consists in 3 self-applied solitary written disclosure sessions (expressive writing).
|
The intervention consists in 3 self-applied solitary written disclosure sessions (expressive writing)
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Subjective health (SF-12)
Tidsramme: 3 months
|
3 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Psychosocial adjustments
Tidsramme: 3 months
|
depression, positive and negative affect, somatic symptoms, adjustment disorder, marital satisfaction, sleep quality
|
3 months
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Lukas Zimmerli, MD, University Hospital Zurich, Internal Medicine
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
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- KEK-ZH 2013-0009_GUGKS
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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