Physical Exercise as Treatment Post-stroke Fatigue - a Feasibilty Study.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: FaStEx - Structured strength training, Control group.
- Who it may be relevant to
- Registry conditions: Stroke, Fatigue Symptom. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Sweden
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The goal of this clinical trial is to evaluate the feasibility the treatment FaStEx (FatigueStrokeExercise) which consists of strength exercise in people with brain fatigue after stroke, referred to as post-stroke fatigue. The main questions it aims to answer are: * What is the feasibility of a study with the treatment FaStEx, structured physical training, for people with post-stroke fatigue? * What factors are important for people with post-stroke fatigue to be able to complete the FaStEx treatment? * How do people with post-stroke fatigue experience participation in the study with the FaStEx treatment? Researchers will compare FaStEx to physical activity at home to see if FaStEx can reduce post-stroke fatigue. Participants will * Carry out strength training twice a week at a health care center. * Carry out physical activity for at least 150 minutes per week on their own. Participants in the control group will carry out this physical activity as well. * The treatment lasts for eight weeks.
Detailed description
Type of treatment FaStEx (FatigueStrokeExercise) - Structured physiotherapist-led exercise intervention.
Dose Strength training for 45 minutes, twice a week for eight weeks.
Components of exercises All training sessions will have the same structure and consist of warm-up, strength training and cool-down.
Each training session starts with a 10-minute warm-up on an exercise bike or through body movements. The strength training is performed as station training with one participant/station. The stations consist of eight different exercises. The participant performs 12 repetitions, 3 sets/exercise, 30 seconds rest between each set. Then rest and transfer to the next station, about 1 min. The load should be 10-12 RM and as a load are used body weight, dumbbells, gym machines, rubber bands, weight cuffs or kettlebells.
Exercises
1. Legs - leg press, squat or raise. 2. Arms - biceps curls (dumbbells or rubber bands). 3. Legs - Knee extension with load (gym machine, weight cuff, rubber band, cable station). 4. Shoulder - lat pull down (gym machine, rubber band). 5. Core - sit-ups or other core training. 6. Shoulder - rowing (cable station, rubber bands, dumbbells). 7. Balance - stand on one leg, tandem standing. 8. Legs - step-up board.
The training session ends with a cool-down through body movements and stretching.
Estimation of exertion with Borg RPE and brain fatigue with VAS before and after the session.
Place The training sessions are carried out in a training room at a health center.
Modifications Alternative exercises will be suggested by the instructor if necessary, e.g. the need for other equipment or support during the exercise. Participants are encouraged to perform the exercises to the best of their ability.
Choice of instructor The instructors are licensed physiotherapists who work in primary care in Region Örebro County who are used to instructing and individualizing training.
Home training In addition to the structured physiotherapist-led training, all participants in the study (control and intervention group) should independently perform aerobic physical activity of at least 150 min/v at a moderate intensity (Borg RPE 12-13). In connection with the start of the intervention, the participants receive an advisory conversation about physical activity to support how they can achieve 150 min/week.
Adherence Participation in strength training will be noted by the treating physiotherapist. Adherence to achieving physical activity for 150 min/w will be followed by participants filling out an activity diary.
Interventions
- Other FaStEx - Structured strength training
Strength training in group session, 2 times a week for 8 weeks. 150 minutes of physical activity per week that is carried out independently. - Other Control group
150 minutes of physical activity per week that is carried out independently.
Primary outcome measures
- Fatigue assessment scale [Time frame: Baseline. End of treament at 8 weeks.]
Secondary outcome measures (8)
- Chair stand test. [Time frame: Baseline. End of treament at 8 weeks.]
- Activities-specific Balance Confidence Scale [Time frame: Baseline. End of treament at 8 weeks.]
- Patient health questionnaire [Time frame: Baseline. End of treament at 8 weeks.]
- 6 minute walking test [Time frame: Baseline. End of treament at 8 weeks.]
- RAND 36 [Time frame: Baseline. End of treament at 8 weeks.]
- Levels of physical activity [Time frame: Measurement will take place 1 week before baseline and 1 week after the intervention at 8 weeks.]
- Sedentary time [Time frame: Measurement will take place 1 week before baseline and 1 week after the intervention at 8 weeks.]
- Levels of physical activity (self-reported) [Time frame: Measurement will take place continuously from baseline to end of treatment at 8 weeks]
Eligibility criteria
Inclusion criteria
\- Stroke ≥6 months, able to move independently ≥100 meters with or without a walking aid, speak Swedish, Fatigue assessment scale (FAS) ≥24 points
Exclusion criteria
- Other neurological disease. Severe impairment of vision, hearing and/or cognition that prevents participation in the intervention. Already performs structured strength training (e.g. gym, group training) regularly (at least 1 time/week).
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Sweden · 1 center
- Region Örebro county — Örebro
Identifiers
NCT: NCT07206147 · 282165