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Effect of Feedback-Based Education on Pain, Fatigue, and Quality of Life

Effect of Feedback-Based Education on Pain, Fatigue, and Quality of Life in Patients with HTLV-1–Associated Myelopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251228068479N1
Enrollment
10
Registered
2026-05-05
Start date
2026-06-05
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

HTLV-1–associated myelopathy. Tropical spastic paraplegia

Interventions

Intervention 1: Intervention group: Patients with HTLV-1–associated myelopathy participate in a feedback-based educational program consisting of one face-to-face session and 3–4 virtual sessions via t

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Written informed consent and willingness to participate in the study. Ownership of a smartphone and ability to use the Eitaa messaging app. Age = 18 years. Minimum literacy (basic reading and writing skills). No severe visual or hearing impairment that would prevent receiving education. Confirmed diagnosis of HTLV-1–associated myelopathy by a neurologist. No cognitive impairment according to the treating physician. At least six months have passed since the diagnosis of the disease. No participation in any formal educational program related to the disease in the past six months.

Exclusion criteria

Exclusion criteria: Unwillingness to participate in the study Severe addiction or active psychiatric disorder Severe acute or chronic disabling disease Severe stress or exposure to major stressful events in the past 6 months

Design outcomes

Primary

MeasureTime frame
Quality of Life. Timepoint: Quality of life will be assessed at baseline (before the intervention), immediately after the intervention, and one month post-intervention. Method of measurement: Thirty-Six-Item Short Form Health Survey Questionnaire.;Fatigue. Timepoint: Fatigue will be measured at baseline (before the intervention), immediately after the intervention, and one month post-intervention. Method of measurement: Fatigue Severity Scale.;Pain Intensity. Timepoint: Pain intensity will be measured at baseline (before the intervention), immediately after the intervention, and one month post-intervention. Method of measurement: Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidreza Zendehtalab

Mashhad University of Medical Sciences

ZendehtalabHR@mums.ac.ir+98 51 3884 6730

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026