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Aerobic Exercise Therapy and Cognitive Behavioural Therapy in Amyotrophic Lateral Sclerosis: effects on activities and quality of life.

Aerobic Exercise Therapy and Cognitive Behavioural Therapy in Amyotrophic Lateral Sclerosis: effects on activities and quality of life.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20642
Enrollment
75
Registered
2009-01-06
Start date
2009-03-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amyotrophic Lateral Sclerosis, Quality of life, Cognitive Behavioural Therapy, Aerobic Exercise therapy, Neuromuscular diseases. Amyotrofische Lateraal Sclerose (ALS), Kwaliteit van Leven, Cognitieve GedragsTherapie, Aerobe Fysieke Training, NeuroMusculaire Ziektes

Interventions

(Exp. group 1) AET + usual care. AET consists of aerobic exercises for a period of 16 weeks, 3 days a week, twice at home and once a week in an individually guided group session in a hospital or rehab

Sponsors

University Medical Centre Utrecht, Department of Rehabilitation
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 70 years; 2. A life-expectancy longer than one year; 3. Forced Vital Capacity at least 80%; 4. Diagnosis of "Probable" of "definite" ALS according to the "revised El Escorial WFN criteria"; 5. At least 3 months post-diagnosis ALS; 6. Being in the rehabilitation phase; diagnotic phase is completed; 7. Walking-ability with or without a ankle-foot orthotic or stick and cycling-ability on a bicycle ergometer, in that capacity that the intervention is expected to be completed.

Exclusion criteria

Exclusion criteria: 1. Cognitive impairment; 2. Insufficient mastery of the Dutch language; 3. Disabling co-morbidity interfering with the intervention programs or influencing outcome parameters (including severe cardiopulmonair disease, like chest pain, arrhytmia, pacemaker, cardiac surgery, sever dyspnoea d'effort or emphysema, epileptic seizures, poorly regulted diabetes mellitus or hypertension; 4. Psychological disorder, in that capacity that the intervention could not be completed.

Design outcomes

Primary

MeasureTime frame
Quality of Life and activities.

Secondary

MeasureTime frame
1. Functional capacity of the patient: cardiorespiratory fitness, strength endurance of the quadriceps, isokinetic muscle strength of the quadriceps, lung function, functional tests, fatigue and pain; 2. Cognitive behavioural aspects of the patient: coping, illness cogitions, personality, mood, impact of event, competences, social suppport; 3. Partner of the patient: quality of life, coping, mood, caregiver strain.

Contacts

Public ContactA.C. Groenestijn, van

Revalidatiecentrum De Hoogstraat Rembrandtkade 10

a.v.groenestijn@dehoogstraat.nl+31 30 2561362

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)