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Completed

NCT Number: NCT04945876

Exercise Adherence and Optimal Nutrition Post Rehabilitation Among People With Parkinson's Disease

A randomized, controlled trial to evaluate the effect of six months digital follow-up, after a stay at a rehabilitation center, on functional and nutritional status in people with Parkinson Disease.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Unicare Fram Rykkin

Rykkin, Bærum, 1349, Norway

About this study

It is found that regular, structured exercise is especially important for people with Pakinson disease (PD) and it is a key element in the treatment of PD at rehabilitation centers in Norway. A substantial amount of research indicate that exercise can lead to improvements in physical functioning, strength, balance, gait, and HRQOL among people with PD. However, after a supervised exercise period, these measures tend to return toward baseline values. This regression may to some extent reflect the progressive nature of PD, but previous research suggests that maintaining the motivation to stay physically active is difficult once formalized interventions end. Furthermore, research indicate that nutritional status is an important predictor for health status among people with PD and that PD patients have high rates of unintentional weight loss compared to age-matched controls. In other words, research indicate that follow-up at home after rehabilitation is necessary to increase optimal nutrition and continuing to exercise.

This is a randomized controlled trial meant to evaluate the effect of six months digital follow-up, after a 3-5 week stay at a inpatient rehabilitation center, on functional and nutritional status in people with PD.

Eligible participants will be recruited from Unicare Fram Rehabilitation center by a physical therapist and research assistant in collaboration with Unicare Fram employees and a Ph.D student. Informed consent from the participants is obtained from persons with no previous relationship to the patients, and who are not included in their daily treatment, mainly the research assistant. After baseline testing the participants will be randomly allocated to an intervention- or control group.

The intervention in this study is designed to increase the level of adherence after rehabilitation by implementing factors that previous studies have proven successful such as education, goal setting, follow-up from health care personnel and use of mHealth Technology. The intervention consist of 2 phases.

Phase 1: All participants will receive the rehabilitation program currently provided at Unicare Fram rehabilitation center. This is a comprehensive and interdisciplinary rehabilitation program with focus on self-management of the disease including exercise and nutrition.

Phase 2: The control group will receive no further follow-up. The intervention group will receive digital follow up once a month focusing on goals and motivation, and an activity tracker and instructions on how to use it both for motivation, daily activity tracking, logging of specific exercise and intensity control.

All participants will be retested after 12 weeks and 6 months at Unicare Fram rehabilitation center by the research assistant.

Descriptive data will be reported for variables of interest. The data will be analyzed following the intention to treat principle. Prospective differences in primary and secondary outcomes and baseline characteristics between the intervention group and the control group will be assessed by t-tests for continuous and normal distributed variables and with non-parametric tests for categorical variables. Multiple linear and logistic regression modelling will be used to control for confounding of between-group differences. The latest version of Statistical Package of the Social Sciences (SPSS) will be used.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >40 years
  • Living at home
  • Living max 2,5 hours travel distance from Unicare Fram
  • A diagnosis of idipathic PD
  • Hoehn-Yahr stage 1-3
  • eternal feeding ability
  • must own a smart phone

Exclusion criteria

  • Hoehn-Yahr stage 4-5
  • Medical issues that might affect participation in exercise programs
  • Diagnosis of dementia
  • Diagnosis of severe dysphagia
  • Exercises regularly more than twice a week(structured exercise).

Treatment and study plan

Digital follow-up

Behavioral

Participants will receive:

One session of individual exercise and diet guidance focusing on goals and motivation.

An activity tracker and instructions on how to use it both for motivation, daily activity tracking, logging of specific exercise and using the wristbands heart rate monitor to control intensity level during exercise.

Monthly digital follow-up to provide support and address questions and goals regarding nutrition, daily energy expenditure and exercise.

Opportunity to send sms with questions regarding nutrition and exercise. Participants who are malnourished, or at risk of malnutrition will be offered a total of two hours of additional individualized, digital guidance on nutrition as needed.

Primary outcomes

  1. Six minute walk test (6MWT)

    Time frame: measured at baseline, 12 weeks and 6 months

    A sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity. It evaluates the functional capacity of the individual.

Secondary outcomes

  1. The Parkinson's disease questionnaire (PDQ-39)

    Time frame: measured at baseline, 12 weeks and 6 months

    A 39 item, patient reported measure of health status and quality of life over the last month. It assesses how often people affected by parkinson's experience difficulties across 8 dimensions of daily living including relationships, social situations and communication. The answers results in a score from 0-100 points in each dimension. Lower scores reflect better QoL.

  2. The Patients-Generated subjective Global Assessment Short Form (PG-SGA)

    Time frame: measured at baseline, 12 weeks and 6 months

    It is a component of a nutritional assessment tool wich could be used for descriptive nutrition screening. A 4 item questionnaire assessing weight, food-intake, symptoms affecting food intake and activity & function. The answers result in a score from 0-9, 0 indicates no need for nutritional measures, 9 indicates a critical need for nutritional measures.

  3. mini best test

    Time frame: measured at baseline, 12 weeks and 6 months

    The test is used to identify risk of falling, changes in balance over time and distinguish between different balance challenges.

  4. and 5x sit-to-stand

    Time frame: measured at baseline, 12 weeks and 6 months

    Assesses functional lower extremity strength, transitional movements, balance and fall risk

  5. Bioelectrical impedance analysis

    Time frame: measured at baseline, 12 weeks and 6 months

    A method for estimating body composition, in particular body fat and muscle mass.

  6. What do you eat

    Time frame: measured at baseline

    A food frequency questionnaire used to assess the diet of a population during the last seven days. Contains questions on how often and how much you eat of specific food groups. The questionnaire does not result in a score. it can be used to raise awareness and to assess on what areas potential nutritional measures is needed.

  7. Radboud Oral Motor Inventory for Parkinson's disease (ROMP) - swallowing

    Time frame: measured at baseline, 12 weeks and 6 months

    A self-report questionnaire with 7 questions assessing potential swallowing difficulties. The answers results in a score from 7-35 point. A low score indicates little to no problems with swallowing, i high score indicates a higher degree of problems with swallowing.

Sponsors and collaborators

Lead sponsor

Oslo Metropolitan University

Other

Collaborators

  • Aalborg University Hospital
  • Fysiofondet
  • Karolinska Institutet
  • Lovisenberg Diaconal University College
  • Norwegian Parkinson's Association
  • Unicare Fram

Registry information

Official study title

Effect of Mobile Health Technology (mHealth), Exercise Adherence and Optimal Nutrition Post Rehabilitation Among People With Parkinson's Disease

Acronym: mHEXANUT

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jun 30, 2021
Registry last updated
Jun 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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