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Chronical Illness-related Limitations of the Ability to Cope With Rising Temperatures, Third Wave (CLIMATE-III)

U

Universitätsklinikum Hamburg-Eppendorf

Status

Enrolling

Conditions

Diabetes Mellitus, Type 1
Ischemic Attack, Transient
Stroke
Peripheral Artery Disease
Arrhythmias, Cardiac
Myocardial Infarction
Heart Failure
Anxiety Disorders
Diabetes Mellitus, Type 2
Asthma
Schizophrenia
Peripheral Nervous System Diseases
Pulmonary Disease, Chronic Obstructive
Renal Insufficiency
Coronary Disease
Depressive Disorder

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT06890208
LPEK-0887

Details and patient eligibility

About

The CLIMATE-III Observational Study examines to what extent chronically ill patients experience adverse health effects because of heat and whether the patients' specific health behavior, somatosensory amplification, risk and benefit perception, self-efficacy, health literacy, and the degree of urbanisation of the patients' administration district are associated with these effects. Study participants from Germany and Italy will be included in the sample.

Full description

The CLIMATE-III Observational Study aims to analyse to what extent chronically ill patients experience adverse health effects because of heat and whether the patients' specific health behavior, self-efficacy, or other factors are associated with these effects. This cohort study is based on an online survey of patients with chronic illness who are recruited in general practitioner (GP) practices in Germany and Italy. After the baseline assessment, participants fill out symptom diaries on 12 specific days of observation over a maximum period of 12 weeks. The specific days of observation are selected based on the maximum temperature that can be expected within the respective weeks. The weather forecast will be checked every Monday. If, in the upcoming 4 days, the maximum temperature is expected to exceed 30°C, the warmest day in this time frame will be chosen. Otherwise, the weather forecast will be checked again on Thursday to choose the warmest of the remaining days of the week. On each day of observation, patients are notified by email at 6 pm.

Baseline assessment includes socio-demographic data, chronic diseases, somatosensory amplification, perceived risk for adverse health effects of heat, intention to implement protective behaviour, perceived benefit of this behavior, self-efficacy, and health literacy. Local data on temperatures and humidity will be provided by the meteorological services of Germany and Italy. Data will be analyzed by multivariable, multilevel regression analyses adjusted for possible confounders and random effects on the administration district and practice within administration district level.

Enrollment

240 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • being 18 years or older
  • at least one of the following conditions: Coronary Heart Disease; Myocardial Infarction; Heart Failure; Cardiac Arrhythmias; Peripheral Artery Disease; Stroke; Transient Ischemic Attack; Diabetes Mellitus (Type 1 or 2); Chronic Obstructive Pulmonary Disease; Asthma; Renal Insufficiency; Depressive Disorder; Anxiety Disorders; Schizophrenia; Peripheral Nervous System Diseases.

Exclusion criteria

  • no capacity to consent
  • severe visual impairment
  • insufficient German language skills
  • not able to use internet browser (eg, lack of hardware)

Trial design

240 participants in 1 patient group

No intervention
Description:
No intervention
Treatment:
Other: No intervention

Trial contacts and locations

1

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Central trial contact

Valentina Paucke

Data sourced from clinicaltrials.gov

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