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Randomized clinical trial evaluating the applicability of remote rehabilitation in patients with lordosis (decrease, increase), kyphosis and scoliosis

Randomized clinical trial evaluating the applicability of remote rehabilitation in patients with lordosis (decrease, increase), kyphosis and scoliosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230206057342N1
Enrollment
46
Registered
2024-04-18
Start date
2022-04-21
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

Kyphosis and lordosis, Scoliosis. Kyphosis and lordosis ,Scoliosis

Interventions

1-Exercises for the patients of "neck lordosis reduction control group" neck muscle training + resistance exercises" and "shoulder raising exercise" and "lateral tilting of the head" and "neck muscle

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: The age of the patients is 20 to 50 years. Patients who have disorders in daily life activities. Patients who have lordosis (decrease, increase), kyphosis and scoliosis and are associated with repeated pain.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: At the beginning, 14 days and 3 months after starting sports training. Method of measurement: Visual pain scale questionnaire.;Functional disability of the back. Timepoint: At the beginning, 14 days and 3 months after starting sports training. Method of measurement: Oswestry questionnaire.;Functional disability of the neck. Timepoint: At the beginning, 14 days and 3 months after starting sports training. Method of measurement: Northwick Park pain questionnaire.;Fear of movement. Timepoint: At the beginning and at the end of the study. Method of measurement: Patient's fear of movement questionnaire.;Anxiety. Timepoint: At the beginning and at the end of the study. Method of measurement: Patient anxiety questionnaire.

Secondary

MeasureTime frame
1- Decreased activity level and quality of life. Timepoint: 1- At the beginning of the study, 2 weeks and 3 months later. Method of measurement: 1- "Oswestry 10-question questionnaire, Northwick Park 9-question pain questionnaire and visual pain scale".;2- Daily life activities. Timepoint: 2- At the beginning of the study, 2 weeks and 3 months later. Method of measurement: 2- "10-question Oswestry questionnaire, 9-question North Wake Park pain questionnaire and visual pain scale".;3-Injury or avoidance of accompanying activity. Timepoint: 3- At the beginning and end of the study. Method of measurement: 3- "Questionnaire of 11 questions of fear of movement".;4- Functional injuries at work. Timepoint: 4- At the beginning and end of the study. Method of measurement: 4- "7-Questionnaire of Anxiety".

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoheila yakhchidor

Kerman University of Medical Sciences

syakhchidor@gmail.com+98 34 3226 3815

Outcome results

None listed

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