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Effect of Physical Training in Individuals With Hypokalemic and Hyperkalemic Periodic Paralysis

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Rigshospitalet

Status

Not yet enrolling

Conditions

Hyperkalemic Periodic Paralysis
Hypokalemic Periodic Paralysis

Treatments

Other: Strength exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07194174
H-25003151

Details and patient eligibility

About

This study wishes to investigate the effects of strength exercise in patients with either HypoPP or HyperPP.

The investigators wishes to include participants already diagnosed with either HypoPP or HyperPP in af 24 week prospective study where the patients will be tested and asked to fill out questionnaires three times. These appointments will be schedueled at week 0, week 12 and week 24.

In the time period between week 12 and week 24, the patients will have a personalized strength exercise program, which they will have to follow these 3 months. The exercise will be supervised by one or more of the investigators.

Enrollment

36 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with genetic verified HypoPP or HyperPP
  • Age minimum 18 years
  • Able to walk a minimum of 10 meters independently with or without assistive devices and be able to stand from a chair without using hands

Exclusion criteria

  • Other significant cause of muscle weakness
  • Heart or lung disease which, in the investigator's opinion, makes participation in the study training inadvisable

Exclusion from muscle biopsy

  • Anticoagulant treatment
  • Impaired blood clotting due to disease

Exclusion from MRI scanning due to:

  • Metal implants in the body that contraindicate MRI scanning or are positioned such that the scan quality is significantly affected
  • Claustrophobia
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

36 participants in 1 patient group

Hypo-/HyperPP
Experimental group
Description:
Strength exercise will be implemented for all participants included in this study. The first 12 weeks will be without intervention and after this period the intervention will begin. The participants are therefore all controls (no intervention) and experimental (intervention).
Treatment:
Other: Strength exercise

Trial contacts and locations

0

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Central trial contact

Annica B Enegaard

Data sourced from clinicaltrials.gov

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