EFFICACY OF ARTIFICIAL INTELLIGENCE DRIVEN PROGRAM VERSUS TRADITIONAL PHYSICAL THERAPY PROGRAM IN PATIENTS WITH LOW BACK DYSFUNCTION (AI-LBD)
5. august 2026 opdateret af: Dalia Ashraf Mohamed Youssef, Cairo University
Efficacy of an Artificial Intelligence-Driven Program Versus a Traditional Physical Therapy Program in Patients With Low Back Dysfunction
Low back dysfunction is one of the most common musculoskeletal disorders and is associated with pain, disability, and reduced quality of life.
Artificial intelligence (AI) has emerged as a promising tool to support personalized rehabilitation by improving exercise prescription, monitoring adherence, and providing real-time feedback.
This randomized controlled trial aims to compare the effectiveness of an AI-driven rehabilitation program with a traditional physical therapy program in patients with low back dysfunction.
Primary outcomes include pain intensity, functional disability, and quality of life.
The findings may provide evidence regarding the role of AI-assisted rehabilitation in improving clinical outcomes.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study is a prospective randomized controlled trial designed to evaluate the efficacy of an artificial intelligence-driven rehabilitation program compared with a traditional physical therapy program in patients with low back dysfunction.
Eligible participants will be randomly allocated into two groups.
The experimental group will receive an AI-driven rehabilitation program, while the control group will receive a standardized traditional physical therapy program.
Clinical outcomes will be assessed before and after the intervention using validated outcome measures for pain, functional disability, quality of life, and other variables specified in the study protocol.
The study aims to determine whether integrating artificial intelligence into rehabilitation provides superior clinical outcomes compared with conventional physical therapy.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
68
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Dalia A Youssef, MSc, PT
- Telefonnummer: +20 101 578 8109
- E-mail: Daliayoussef151023@gmail.com
Studiesteder
-
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Cairo Governorate
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Cairo, Cairo Governorate, Egypten
- Faculty of Physical Therapy, Cairo University
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- Adults aged 18-45 years.
- Male or female participants.
- Clinical diagnosis of low back dysfunction by a physiotherapist or physician.
- Symptoms lasting more than 3 months.
- Ability to participate in physical therapy or use AI-based rehabilitation tools.
- Willingness to comply with the study protocol and provide written informed consent.
Exclusion Criteria:
- Recent spinal injury or spinal surgery.
- Previous spinal surgery within the last 6 months.
- Severe neurological disorders (e.g., multiple sclerosis or Parkinson's disease).
- Chronic conditions that significantly limit mobility (e.g., advanced arthritis).
- Current use of strong opioid analgesics.
- Severe psychiatric disorders.
- Inability to use or access the required technology for the AI intervention.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: AI-Driven Rehabilitation
Participants will receive an artificial intelligence-driven rehabilitation program including personalized exercise prescription, progression, and monitoring according to the study protocol.
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A personalized rehabilitation program guided by artificial intelligence, including individualized exercise prescription and progression.
|
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Aktiv komparator: Traditional Physical Therapy
Participants will receive a standardized traditional physical therapy rehabilitation program according to the study protocol.
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A conventional physical therapy rehabilitation program delivered according to the study protocol
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Pain Intensity
Tidsramme: Baseline and immediately post intervention 6 weeks of treatment.
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Pain intensity measured using the Visual Analogue Scale (VAS), a 10-cm self-reported pain scale ranging from 0 (no pain) to 10 (worst imaginable pain).
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Baseline and immediately post intervention 6 weeks of treatment.
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Functional Performance
Tidsramme: Baseline and after 6 weeks.
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Functional performance measured using the Back Performance Scale (BPS).
The total score ranges from 0 to 15, with higher scores indicating greater functional limitation.
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Baseline and after 6 weeks.
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Cost-effectiveness
Tidsramme: After completion of the 6-week intervention.
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Cost-effectiveness assessed using the Incremental Cost-Effectiveness Ratio (ICER), based on total costs and clinical effectiveness of the AI-driven and traditional physical therapy programs,including direct medical costs, intervention-related costs, and healthcare utilization costs.
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After completion of the 6-week intervention.
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Lumbar Range of Motion
Tidsramme: Baseline and after 6 weeks.
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Lumbar range of motion assessed using the Back Range of Motion (BROM II) device measuring lumbar flexion, extension, lateral flexion, and rotation.
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Baseline and after 6 weeks.
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. august 2026
Primær færdiggørelse (Anslået)
1. december 2026
Studieafslutning (Anslået)
1. januar 2027
Datoer for studieregistrering
Først indsendt
3. august 2026
Først indsendt, der opfyldte QC-kriterier
3. august 2026
Først opslået (Faktiske)
6. august 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
7. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
5. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- AI-LBD-20260803-1995-DA
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
Individual participant data will not be publicly shared to protect participant confidentiality and privacy.
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