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Resistance Intensive Personal Training (RIPT) for Resistance Training (RIPT Trial)

N/A
Recruiting
Led By Elizabeth Condliffe
Research Sponsored by University of Calgary
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
17 years old or younger
At least 8 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 weeks (from time of consent to end of trial).
Awards & highlights

RIPT Trial Summary

This trial aims to investigate if a specialized power training program called RIPT can help improve the motor function of youth with Cerebral Palsy. This program is not currently available in Calgary but will be

Who is the study for?
This trial is for young people with Cerebral Palsy, aged 8 to 17 years old, who can understand English and are capable of exerting maximum effort in physical activities. It's not suitable for those who don't meet these age or communication requirements.Check my eligibility
What is being tested?
The study tests a Resistance Intensive Personal Training program designed to improve muscle strength and motor function in youth with CP. The effectiveness and feasibility of delivering this training through a community-hospital partnership are being evaluated.See study design
What are the potential side effects?
While specific side effects aren't listed, resistance training may cause muscle soreness, fatigue, or discomfort especially when starting a new exercise regimen. Close monitoring will ensure safety for participants.

RIPT Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 17 years old or younger.
Select...
I am at least 8 years old.

RIPT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~14 weeks (from time of consent to end of trial).
This trial's timeline: 3 weeks for screening, Varies for treatment, and 14 weeks (from time of consent to end of trial). for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Canadian Occupational Performance Measure
Goal Attainment Scale
Secondary outcome measures
EQ-5D-Y
Gross Motor Function Measure
Muscle power assessment

RIPT Trial Design

1Treatment groups
Experimental Treatment
Group I: Resistance Intensive Personal Training (RIPT)Experimental Treatment1 Intervention
All participants will participate in this arm involving 12 weeks of training 2-3 days/week in a group setting with each session involving 1:1 support for each participant's power training.

Find a Location

Who is running the clinical trial?

University of CalgaryLead Sponsor
796 Previous Clinical Trials
874,765 Total Patients Enrolled
Elizabeth CondliffePrincipal InvestigatorUniversity of Calgary
~10 spots leftby Jun 2025
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