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The Effect of Dignity Therapy on Quality of Life and Life Satisfaction in Patients with Heart Failure

Investigating the Effect of In-Person and Virtual Dignity Therapy on Quality of Life and Life Satisfaction in Patients with Heart Failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250714066482N1
Enrollment
90
Registered
2025-07-15
Start date
2025-08-05
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Patients with heart failure. Heart failure

Interventions

Intervention 1: Intervention group: In the in-person group, the intervention is carried out through a structured process consisting of three face-to-face sessions, each lasting 30 to 60 minutes, with

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of class II, III, or IV heart failure based on the New York Heart Association (NYHA) classification by a specialist physician Willingness and informed consent to participate in the study Absence of severe illness-related conditions that would prevent participation in the intervention Mental health stability and no significant psychological issues such as severe anxiety, depression, suicidal thoughts, obsessive-compulsive disorder, or other psychological disorders, according to the patient’s medical records Ability to use a smartphone and access the internet Adequate hearing and speaking abilities to participate in interviews Minimum literacy in reading and writing in Persian No cognitive impairments Age over 18 years

Exclusion criteria

Exclusion criteria: Lack of willingness to continue participation in the study Deterioration of the patient's health condition Participation in educational or therapeutic sessions similar to the intervention Death Re-hospitalization

Design outcomes

Primary

MeasureTime frame
?Quality of life. Timepoint: Before intervention and one month after the end of intervention. Method of measurement: Chronic heart failure health-related quality of life questionnaire (CHFQOLQ-20).;Life satisfaction. Timepoint: Before intervention and one month after the end of intervention. Method of measurement: Satisfaction With Life Scale (SWLS).

Secondary

MeasureTime frame
Anxiety. Timepoint: Before the intervention and one month after the end of the intervention. Method of measurement: Generalized Anxiety Disorder (GAD-7).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Khedmatizare

Tehran University of Medical Sciences

mahsa.khzare@gmail.com+98 21 6692 7171

Outcome results

None listed

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