This study is a randomised control trial and the purpose of this study is to determine comparision of Kaltenborn Mobilization and Mobilization with Movement (MWM) in wrist Hpomobility after Colle's fracture.
Age range
40 Years – 70 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Range of Motion at wrist
Timeframe: 1st measurement taken before starting session (Baseline measurement) 2nd or post measurement taken after end of sessions (after 3 weeks) (2 points measurement would be taken) 9 treatment sessions in 3 weeks is total time period.
Wrist Pain
Timeframe: 1st measurement taken after 3 or 4 sessions of treatment 2nd or last/post measurement taken at end of session (after 3 weeks) (2 points measurement would be taken).
Functional disability
Timeframe: 1st measurement taken after 3 or 4 sessions of treatment 2nd or last/post measurement taken at end of session (after 3 weeks) 2 points measurement would be taken)