Evidence map›Paper›PMID 38638511›Full record

ArticleFrontiers in psychology2024

Coping as a resource to allow for psychosocial adjustment in fatal disease: results from patients with amyotrophic lateral sclerosis.

Julia Finsel, Angela Rosenbohm, Raphael S Peter, Hansjörg Bäzner, Axel Börtlein, Silke Dempewolf, Martin Schabet, Martin Hecht, Andreas Kohler, Christian Opherk and 7 more

Abstract read
In one paragraph

Article in Frontiers in psychology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Palliative Care Involvement in Hospitalized Amyotrophic Lateral Sclerosis Patients.International journal of environmental research and public health · 2026
    Article
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Julia FinselDepartment of Neurology, Ulm University, Ulm, Germany.
Angela RosenbohmDepartment of Neurology, Ulm University, Ulm, Germany.
Raphael S PeterInstitute for Epidemiology and Medical Biometry, Ulm University, Ulm, Germany.
Hansjörg BäznerDepartment of Neurology, Katharinenhospital Stuttgart, Stuttgart, Germany.
Axel BörtleinDepartment of Neurology, Katharinenhospital Stuttgart, Stuttgart, Germany.
Silke DempewolfDepartment of Neurology, RKH Klinikum Ludwigsburg, Ludwigsburg, Germany.
Martin SchabetDepartment of Neurology, RKH Klinikum Ludwigsburg, Ludwigsburg, Germany.
Martin HechtDepartment of Neurology, Klinikum Kaufbeuren, Kliniken Oberallgäu-Kaufbeuren, Kaufbeuren, Germany.
Andreas KohlerDepartment of Neurology, Klinikum am Gesundbrunnen Heilbronn, Heilbronn, Germany.
Christian OpherkDepartment of Neurology, Klinikum am Gesundbrunnen Heilbronn, Heilbronn, Germany.
Andrea NägeleDepartment of Neurology, Christophsbad Göppingen, Göppingen, Germany.
Norbert SommerDepartment of Neurology, Christophsbad Göppingen, Göppingen, Germany.
Alfred LindnerDepartment of Neurology, Marienhospital Stuttgart, Stuttgart, Germany.
Dietrich RothenbacherInstitute for Epidemiology and Medical Biometry, Ulm University, Ulm, Germany.
Albert C LudolphDepartment of Neurology, Ulm University, Ulm, Germany.
Gabriele NagelInstitute for Epidemiology and Medical Biometry, Ulm University, Ulm, Germany.
Dorothée E LuléDepartment of Neurology, Ulm University, Ulm, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Amyotrophic lateral sclerosis (ALS) is a fatal disorder, which imposes a severe emotional burden on patients. Appropriate coping mechanisms may alleviate this burden and facilitate wellbeing, with social support known to be a successful coping strategy. This observational study aimed to determine the interplay of general coping traits of hope for success and fear of failure, coping behavior of social activity, and patients' wellbeing. Methods: In this cross-sectional study, patients with ALS from a clinical-epidemiological registry in Southwestern Germany were interviewed regarding coping traits (achievement-motivated behavior: hope for success and fear of failure), coping behavior of social activity, and psychosocial adjustment, determined using measures of depressiveness, anxiety [both measured by Hospital Anxiety and Depression Scale (HADS)], and quality of life [Anamnestic Comparative Self-Assessment (ACSA)]. Demographics, clinical [ALS Functional Rating Scale revised version (ALSFRS-R)], and survival data were recorded. Results: A total of 868 patients [60.70% male patients, mean age: 64.70 (±10.83) years, mean ALSFRS-R: 37.36 ± 7.07] were interviewed. Anxiety in patients was found to be associated with a high fear of failure. In contrast, a generally positive attitude in patients exemplified in high hopes for success was associated with better wellbeing. Finally, coping behavior of social activity explained up to 65% of the variance of depressiveness among the patients with ALS. Conclusion: In this study, we present evidence that the wellbeing of patients with ALS is not an immediate fatalistic consequence of physical degradation but rather determined by coping traits and behavior, which may be trained to substantially increase the wellbeing of patients with ALS.

Indexed as

amyotrophic lateral sclerosiscopingdepressivenesspsychosocial adaptationquality of lifewellbeing

Identifiers

PMID38638511
PMCPMC11024296

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.