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Couples Coping With Multiple Chronic Medical Conditions

Couples Coping With Multimorbidity: Does Solitary Expressive Writing Foster Psycho-social Adaptation?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01912157
Acronym
GUGKS
Enrollment
22
Registered
2013-07-30
Start date
2013-07-31
Completion date
2018-12-28
Last updated
2018-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Disease, Illness Behavior

Brief summary

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)

Detailed description

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)

Interventions

BEHAVIORALExpressive Writing

The intervention consists in 3 self-applied solitary written disclosure sessions (expressive writing)

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Subjective health (SF-12)3 months

Secondary

MeasureTime frameDescription
Psychosocial adjustments3 monthsdepression, positive and negative affect, somatic symptoms, adjustment disorder, marital satisfaction, sleep quality

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026