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Internet-based Self-help After Spousal Bereavement or Divorce

Evaluation of a Randomised Guided Internet-based Self-help Intervention for Older Adults Who Seek Support for Coping With Prolonged Grief Symptoms After Marital Bereavement or Divorce - LIVIA

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02900534
Acronym
LIVIA
Enrollment
110
Registered
2016-09-14
Start date
2016-05-31
Completion date
2018-05-06
Last updated
2018-10-22

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

Conditions

Prolonged Grief Symptoms

Keywords

grief, depression, bereavement, divorce, online self-help

Brief summary

The purpose of this study is to evaluate the efficacy of an internet-based self-help intervention for older adults with prolonged grief symptoms after spousal bereavement or separation/divorce. The study design is a randomized trial with a waiting control condition of 12 weeks and a follow-up after 6 months. The investigators will test the following main hypotheses: 1. The intervention group shows a significant decrease in grief symptoms, psychological distress, depression symptoms and embitterment, and a significant increase in life satisfaction, as well as session related outcomes from baseline to 12 weeks post intervention assessment. 2. The effects in the intervention group are larger than the effects in the waiting control group. 3. These effects are stable from the post measure at 12 weeks to the 6-month follow-up.

Interventions

10 internet-based self-help sessions plus one supportive email a week with a cognitive-behavioural background

Sponsors

University of Bern
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Marital bereavement or separation/divorce. Both events should have happened more than 6 months before participating in the study. * Seeking support for coping with grief symptoms * Internet access * Mastery of the German language * Informed Consent

Exclusion criteria

* Acute suicidality (BDI Suicide item \> 1 or suicidal ideation in the telephone interview) * No emergency plan: In the telephone interview, an emergency plan will be developed which specifies a health care professional, who participants can turn to in an acute crisis. If no such person or health care service can be found, individuals will be excluded from the intervention. * Severe psychological or somatic disorders which need immediate treatment. * Concomitant psychotherapy (participants may take part in the self-help intervention, but will not be included in the study.) * Prescribed drugs against depression or anxiety lead to an exclusion if prescription or dosage has changed in the month prior or during the self-help intervention. * Inability to follow the procedures of the study, e.g. due to comprehension problems

Design outcomes

Primary

MeasureTime frameDescription
Grief symptoms12 weeks after the start of the interventionTexas Revised Inventory of Grief (German version, Znoj,2008; Faschingbauer, 1981)
Psychological distress12 weeks after the start of the interventionBrief Symptom Inventory (German version, Franke, 2000)

Secondary

MeasureTime frameDescription
Depression symptoms12 weeks after the start of the interventionBeck Depression Inventory II (German version, Hautzinger, Kühne & Keller, 2006)
Satisfaction with life12 weeks after the start of the interventionSatisfaction with life scale (German version, Schumacher, 2003)
Embitterment12 weeks after the start of the interventionEmbitterment questionnaire (Znoj &, Schyder, 2014)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026