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The Impact of Remote care on the Psychological Well-Being and Caregiving Burden of Families of Psoriasis Patients

Investigating the impact of remote care training on the psychological well-being and caregiving burden of family caregivers of patients with psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240319061338N2
Enrollment
70
Registered
2025-01-17
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Psoriasis. Psoriasis

Interventions

Intervention 1: Intervention group: The intervention in this study involves a one-month remote education program for the intervention group following their discharge from the clinic. The educational c

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Participants aged 18 to 65 years (first-degree family members of the patient, including father, mother, sister, brother, spouse, or child living with the patient). Ownership of a smartphone and access to the internet. Literacy (ability to read and write). Absence of visual and auditory impairments. Non-membership of the patient and their family in the treatment team. No history of diagnosed psychological disorders within the patient's family. Absence of addiction or psychiatric medication use. The patient not having any concurrent skin diseases.

Exclusion criteria

Exclusion criteria: Any dissatisfaction expressed by the family caregivers during the study. Any dissatisfaction expressed by the family caregivers during the study. The death of any participating family caregiver during the study. Incomplete completion of more than 10% of the questionnaires.

Design outcomes

Primary

MeasureTime frame
Psychological well-being score in the Riff questionnaire. Timepoint: Measurement of psychological well-being will be conducted at the beginning of the study (prior to the intervention) and at the end of the study. Method of measurement: Riff Psychological Well-Being Questionnaire (1989).;The caregiver burden score in the Novak and Guest questionnaire. Timepoint: Measurement of family caregiver burden will be conducted at the beginning of the study (prior to the intervention) and at the end of the study. Method of measurement: Novak and Guest Caregiver Burden Inventory (1989).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Zakeri Moghadam

Tehran University of Medical Sciences

zakerimo@gmail.com+98 21 6692 7171

Outcome results

None listed

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