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This study aims to evaluate the effects of rehabilitation programs supported by artificial intelligence-based large language models (LLMs), specifically ChatGPT and DeepSeek, in individuals with subacromial pain syndrome (SAPS). Participants will be randomly assigned to one of three groups: standard physiotherapy, standard physiotherapy plus ChatGPT-guided exercises, and standard physiotherapy plus DeepSeek-guided exercises. Outcomes including pain, disability, quality of life, muscle strength, and joint range of motion will be assessed before and after a 6-week intervention. The results will help determine whether AI-generated exercise recommendations can enhance clinical outcomes when combined with conventional physiotherapy.
Full description
This completed randomized controlled trial investigated the clinical effects of integrating AI-generated exercise recommendations into conventional physiotherapy for individuals with subacromial pain syndrome (SAPS). A total of 82 individuals were assessed for eligibility; 7 were excluded for not meeting inclusion criteria. Seventy-five participants provided consent and were randomized equally to 3 groups (n=25 each): (1) conventional physiotherapy plus a conventional exercise program, (2) conventional physiotherapy plus ChatGPT-guided exercises, and (3) conventional physiotherapy plus DeepSeek-guided exercises. Interventions were delivered over 6 weeks (3 supervised sessions/week).
Six participants discontinued the intervention due to scheduling conflicts (2 per group). Sixty-nine participants completed the 6-week intervention and were included in the final analysis (n=23 per group).
Co-primary outcomes were pain intensity (NPRS: rest, activity, night), shoulder pain and disability (SPADI), and health-related quality of life (SF-12 PCS/MCS), assessed at baseline and 6 weeks. Secondary outcomes included DASH, range of motion, isometric strength (Kinvent K-Force; Newtons), kinesiophobia (TSK), pain catastrophizing (PCS), emotional status (HADS), and shoulder function (ASES, WORC).
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75 participants in 3 patient groups
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Ömer Alperen GÜRSES, PhD
Data sourced from clinicaltrials.gov
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