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The effect of positive thinking interventions on illness perception and symptoms distress

The effect of positive thinking interventions on illness perception and symptoms distress among heart failure patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240506061676N1
Enrollment
70
Registered
2024-05-19
Start date
2024-05-21
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Heart Failure. Heart failure, unspecified

Interventions

Intervention 1: Intervention group: Intervention group by the convenience method, taking into account the inclusion and exclusion criteria of those suffering from heart failure. Applicants will be sel

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Consent to participate in research ability to read and write Age 20-65 years No addiction (alcohol, smoking and drugs) Not going through an emotional crisis in the last 3 months Diagnosis of heart failure by a cardiologist (EF=40%) At least 6 months have passed since the initial diagnosis Not suffering from acute psychiatric disorders (schizophrenia, depression) and taking psychoactive drugs Not participating in similar training courses in the last 6 months. Not having a high level of anxiety and stress based on the DASS-21 questionnaire (stress and anxiety scores should be maximum 12 and 7 respectively) Lack of therapeutic interventions performed to manage heart disease (PCI or CABG) Class I, II and III in the NYHA criteria

Exclusion criteria

Exclusion criteria: Unwillingness to continue participating in the study Experiencing an emotional crisis during the intervention process by the patient Absence in more than 2 sessions of the intervention process

Design outcomes

Primary

MeasureTime frame
Illness Perception Score in the Brief Illness Perception Questionnaire. Timepoint: Before the intervention, immediately after the intervention, two months after the end of the intervention. Method of measurement: Brief Illness Perception Questionnaire.;Symptom Distress Score in Symptom Distress Scale. Timepoint: Before the intervention, immediately after the intervention, two months after the end of the intervention. Method of measurement: Symptom Distress Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Abolfazl Vagharseyyedin

Birjand University of Medical Sciences

Waghars@bums.ac.ir+98 56 3239 5000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026