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Completed

NCT Number: NCT01047410

ACtive Care After Transplantation, the ACT Study

The aim of the present study is to compare the outcomes of standard care to the effects of exercise alone, and exercise combined with nutrition counseling, on post-transplantation weight gain and quality of life in renal transplant recipients (RTR). The primary outcome is subdomain physical functioning of quality of life, (SF-36 PFS).

Secondary outcomes include other evaluations of quality of life (SF-36, KDQOL-SF, EQ-5D), objective measures of physical functioning (aerobic capacity and muscle strength), level of physical activity, gain in adiposity (body fat percentage by bio-electrical impedance assessment, BMI, waist circumference), and cardiometabolic risk factors (blood pressure, lipids, glucose metabolism). Additionally it is planned to study data on renal function, medical history, medication, psychological factors (motivation, kinesiophobia, coping style), nutrition knowledge, nutrition intake, nutrition status, fatigue, work participation, process evaluation and cost-effectiveness.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Reade, Amsterdam, North Holland, Netherlands

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About this study

Patient and graft survival in the first year after renal transplantation have improved substantially over the last decade, but long-term graft loss and patient mortality have remained high. It is increasingly recognized that the alarmingly poor cardio-metabolic risk profile in renal transplant recipients (RTR) plays a main role in long-term outcome. Improvement of long-term outcome will require specific efforts to improve cardio-metabolic profile and its complications. Importantly, the substantial increase in body weight and body fat that occurs after transplantation is a major trigger for the poor cardiometabolic profile in the RTR, including post-transplant diabetes and metabolic syndrome.

The increase in body weight is mostly fat tissue and typically around 9-10 kg. Most of this weight gain (~90%) occurs in the first year after transplantation. Recent data indicate that steroid avoidance could not prevent this early increase in adiposity. This warrants specific focus on lifestyle factors, i.e diet and physical activity. In the UMCG RTR cohort we found that a lack of physical activity was related to a worse cardiometabolic profile and was an independent predictor of mortality. Moreover, the substantial increase in fat massweight gain was strongly related to low physical activity, high intake of energy-dense drinks, low consumption of vegetables, to increased plasma triglycerides and the metabolic syndrome. The intake of salt and saturated fat was high and fibre intake was low, indicating dietary habits that deviate substantially from recommendations for a healthy diet. Thus, both physical activity and dietary habits are important targets for lifestyle intervention in RTR.

Lasting improvements in lifestyle are notoriously difficult to obtain, but in recent years substantial intervention expertise has been developed in other high risk groups including prediabetes. It is now established that for long term purposes, prevention of excessive weight gain is more effective than treatment of weight excess. Since in RTR most of the weight is gained in the first year after transplantation, prevention is a very promising approach. Moreover, data in prediabetes suggest that combined intervention targeting both diet and physical activity may be particularly effective to this purpose.

Therefore, our aim is to investigate the effects on quality of life by a combined diet-and-physical activity program in RTR in the first year after transplantation.

This randomized controlled intervention study will use a combined diet-and-physical activity approach. After hospital discharge for transplantation, 219 patients will be randomized to three either a control groups: one group, who will receive standard care, one group will be exposed to a 3-month exercise program followed by individual counselling and one group will be exposed to the exercise program + dietary or to intervention followed by individual counselling. The individual counselling is to consolidate the achieved improvements in diet and physical activity and will be provided until 15 months after inclusion. This counselling is based on theories of behavioural change and motivational interviewing. Daily physical activity is evaluated with a pedometer and dietary habits by questionnaires and food records.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years;
  • Informed Consent;
  • >1 year after transplantation
  • Medical approvement for participation in the study by the nephrologist.

Exclusion criteria

  • Psychopathology;
  • Severe cognitive disorders;
  • Negative advice of the nephrologist and/or cardiologist.

Treatment and study plan

Exercise intervention

Other

Patients assigned to the exercise intervention participate in a 12 weeks lasting, intensive, standardized and supervised physical training program which consists of a combination of endurance and strength training. After completion of the training program, patients receive an individual sport- and physical activity advice and lifestyle coaching.

Exercise intervention and dietary advice

Other

The exercise intervention in this group is identical to the exercise-only group. The nutritional intervention runs throughout the entire 15 month intervention. The nutritional intervention aims to critically discuss pre-transplantation nutritional habits, and to set goals for healthier, better quality nutrition to prevent over eating and weight gain. These goals are set together with the subject to facilitate an autonomy supportive coaching climate.During the dietary consults, special attention goes out to saturated fat intake, whole-wheat and high fibre foods, fruit and vegetable intake, dietary salt consumption, and the use of energy-rich beverages such as soda, dairy drinks and fruit juices.

Primary outcomes

  1. Quality of life - Physical Functioning Score

    Time frame: baseline, 12 weeks, 6 months and 15 months

    The subdomain 'Physical Functioning' of Quality of Life (SF36 questionnaire)

Secondary outcomes

  1. Quality of Life Scores

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Physical and Mental scores of the Quality of Life SF36 questionnaire

  2. Physical functioning

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Exercise capacity by VO2max test and/or submax test

  3. Physical functioning

    Time frame: baseline, 12 weeks, 6 months and 15 months

    skeletal muscle strength by maximal strenght test

  4. Body composition

    Time frame: baseline, 12 weeks, 6 months and 15 months

    waist circumference

  5. Body composition

    Time frame: baseline, 12 weeks, 6 months and 15 months

    body fat percentage (bioelectrical impedance)

  6. Body composition

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Height and weight to calculate BMI

  7. Cardiometabolic risk factors

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Blood pressure

  8. Cardiometabolic risk factors

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Lipid profiles (cholesterol)

  9. Cardiometabolic risk factors

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Lipid profiles (triglycerides)

  10. Cardiometabolic risk factors

    Time frame: baseline, 12 weeks and 15 months

    glucose metabolism

  11. nutrition

    Time frame: baseline, 12 weeks, (6 months for nutrition intervention only) and 15 months

    dietary intake (food diaries)

  12. nutrition

    Time frame: baseline and 15 months

    nutritional knowledge (questionnaire)

  13. Psychological factors

    Time frame: 12 weeks and 15 months

    motivation (questionnaire)

  14. Psychological factors

    Time frame: baseline and 15 months

    kinesiophobia (questionnaire)

  15. Psychological factors

    Time frame: baseline

    coping style (questionnaire)

  16. Chronic fatigue

    Time frame: baseline, 12 weeks, 6 months and 15 months

    CIS-20 questionnaire

  17. Fatigue and work participation

    Time frame: baseline, 12 weeks, 6 months and 15 months

    Fatigue and work questionnaire (NFR)

  18. Cost-effectiveness

    Time frame: baseline, 12 weeks, 6, 9, 12 and 15 months

    care consumption and intervention costs

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Collaborators

  • Dutch Kidney Foundation
  • Innovation Fund of the Dutch Medical Insurance Companies

Registry information

Official study title

ACtive Care After Transplantation, a Lifestyle Intervention in Renal Transplant Recipients

Acronym: ACT

Important dates

Study start
2010
Primary completion
2017
Study completion
2017
First posted
Jan 12, 2010
Registry last updated
Aug 31, 2018

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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