Tokyo, Dec. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059763) titled 'A Feasibility Study of a Health Education Program in Postoperative Lumbar Rehabilitation' on Dec. 1.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Open -but assessor(s) are blinded
Control - Active
Primary Sponsor:
Institute - Osaka Metropolitan University
Condition:
Condition - Postoperative lumbar surgery patients
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To evaluate the feasibility of a health education program in postoperative lumbar rehabilitation.
Basic objectives2 - Others
Intervention:
Interventions/Control_1 - Intervention group: Total 160 minutes (4 sessions of 40 minutes) during hospitalization. Program includes skills for information acquisition, disease-specific understanding, active action planning, and information sharing with others (health literacy education).
Interventions/Control_2 - Control group: Usual care consisting of standard patient education (40 minutes).
Eligibility:
Age-lower limit - 40
years-old
= 40 years
Provided informed consent
Key exclusion criteria - Patients undergoing reoperation
Patients with severe comorbidities
Patients with cognitive impairment
Patients without electronic devices with search functions
Target Size - 34
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 09 Month 27 Day
Date of IRB - 2025 Year 09 Month 27 Day
Anticipated trial start date - 2025 Year 12 Month 01 Day
Last follow-up date - 2030 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068340
Disclaimer: Curated by HT Syndication.
