PAL: Proactive Automatized Lifestyle Intervention

Sponsor
University Medicine Greifswald (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05365269
Collaborator
Deutsche Krebshilfe e.V., Bonn (Germany) (Other), Robert Koch Institut (Other), University Hospital Schleswig-Holstein (Other)
175
1
1
10
17.5

Study Details

Study Description

Brief Summary

Background: The co-occurrence of health risk behaviors (HRBs), namely of tobacco smoking, insufficient physical activity, unhealthy diet and at-risk alcohol use, more than doubles the risk of cancer, other chronic diseases and mortality; and applies to more than half of adult general populations. However, preventive measures that target all four HRBs and that reach the majority of the target populations and particularly those persons most in need and hard to reach (e.g. with low socio-economic status), are scarce. Electronic interventions may help to efficiently address multiple HRBs in whole populations, such as health care patients. The aim is to investigate the acceptance of a proactive and brief electronic multiple behavior change intervention among general hospital patients with regards to reach, retention, equity in reach and retention, satisfaction and subsequent trajectories of behavior change motivation, HRBs and health.

Methods: A pre-post-intervention study with four time points will be conducted at a general hospital in Germany. Patients admitted to participating medical departments (internal medicine, general surgery, trauma surgery, ear-nose-throat medicine) and aged 18-64 years will be systematically approached and invited to participate, irrespective of reason for admission and HRB profile. Based on HRB profile and on psychological behavior change theory, participants (n=175) will receive individualized computer-generated feedback concerning all four HRBs and motivation-enhancing feedback for up to two HRBs; directly on the ward and 1 and 3 months later. Intervention reach and retention will be determined by the proportion of participants among eligible patients and participants, respectively. Equity in reach and retention will be measured with regards to school education and other socio-demographics. To investigate satisfaction with the intervention and trajectories of motivational measures, HRBs and health measures, a 6-month follow-up will be conducted. Descriptive statistics, multivariate regressions and latent growth modelling will be applied.

Discussion: This study will be the first to investigate the acceptance of a proactive, electronic and brief multiple behavior change intervention among general hospital patients. If reach is high and efficacy established by a randomized controlled trial, the intervention has potential for public health impact in terms of primary and secondary prevention of diseases.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Proactive Automatized Lifestyle intervention
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
175 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Masking Description:
By nature, the participants, investigators and outcomes assessors of the single arm study are informed that an intervention is being (or has been) delivered.
Primary Purpose:
Prevention
Official Title:
Proactive Automatized Lifestyle Intervention for Cancer Prevention
Actual Study Start Date :
May 31, 2022
Anticipated Primary Completion Date :
Mar 31, 2023
Anticipated Study Completion Date :
Mar 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Computer-generated feedback on health risk behaviors

Proactive Automatized Lifestyle intervention Frequency: 3 times (month 0, 1, 3) Dosage: Individually tailored feedback corresponding to about 1-6 pages Duration: 3 months

Behavioral: Proactive Automatized Lifestyle intervention
Multi-behavioral; including individually-tailored, theory-based, repetitive, ipsative and normative feedback.

Outcome Measures

Primary Outcome Measures

  1. Intervention reach [Month 0]

    Proportion of participants among all eligible patients

  2. Intervention retention [Month 1]

    Proportion of participants who continue participation 1 month after hospitalization

  3. Intervention retention [Month 3]

    Proportion of participants who continue participation 3 months after hospitalization

Secondary Outcome Measures

  1. Satisfaction with intervention [Month 6]

    Modified and adapted 29-item Multi-Dimensional Measure of Satisfaction with Behavioral Interventions; assessing process (intervention characteristic ratings, dose and format ratings, usage, overall intervention rating) and outcome (discomfort, attribution of outcomes to treatment)

  2. Change in physical activity [Month 0, 1, 3, 6]

    European Health Interview Survey-Physical Activity Questionnaire, three additional items

  3. Change in diet [Month 0, 1, 3, 6]

    Self-reported number of servings of vegetable and fruit per day; Self-reported intake of fat (gram, kilojoule, kilocalories), fiber (gram), salt (gram) and sugar (gram) per day measured by a 16 item diet screener on the number of servings of vegetable, fruit, other food rich in fiber, sweets, added sugar, sweetened drinks, cheese, convenience food, salted snacks, eggs, fatty fish, red meat, processed meat, butter/ oil, milk and bread per day/ week

  4. Change in alcohol use [Month 0, 1, 3, 6]

    Alcohol Use Disorder Identification Test - Consumption; alcohol use in past month

  5. Change in tobacco smoking [Month 0, 1, 3, 6]

    Self-reported number of cigarettes per day; smoking status

  6. Change in sum of behavioral health risk factors [Month 0, 1, 3, 6]

    Behavioral health risk factors are determined when recommendations (WHO, World Cancer Research Fund, German Center of Addiction Issues) are not met; with the total sum score ranging between 0 and 4 behavioral health risk factors (insufficient physical activity, unhealthy diet, at-risk alcohol use, tobacco smoking)

  7. Change in body-mass-index [Month 0, 6]

    Obtained from self-reported body weight and height

  8. Change in general health [Month 0, 6]

    1 item on self-reported health ranging between poor (0) and excellent (4)

  9. Change in mental health [Month 0, 6]

    5-item Mental Health Inventory; Higher scores indicate better mental health

  10. Change in sick days [Month 0, 6]

    Number of self-reported sick days past 6 months

  11. Change in stage of change [Month 0, 1, 3, 6]

    Behavior-specific staging algorithms based on the transtheoretical model of intentional behavior change (TTM)

  12. Change in decisional balance [Month 0, 1, 3, 6]

    Behavior-specific decisional balance questionnaires based on the TTM; higher scores indicate more pros and cons of physical activity / vegetable and fruit intake / alcohol use / tobacco smoking

  13. Change in self-efficacy [Month 0, 1, 3, 6]

    Behavior-specific self-efficacy questionnaires based on the TTM; higher scores indicate higher self-efficacy to be physically active / to eat vegetable and fruit / to adhere to alcohol use limits / to refrain from tobacco smoking

  14. Change in processes of change [Month 0, 1, 3, 6]

    Behavior-specific processes of change questionnaires based on the TTM; higher scores indicate higher process use in terms of increasing physical activity / eating more vegetable and fruit a day / reducing (or quitting) alcohol use / reducing (or quitting) tobacco smoking

Other Outcome Measures

  1. Change in non-communicable diseases [Month 0, 6]

    Self-reported cardio-vascular disease, chronic respiratory disease, cancer disease, diabetes

  2. Change in utilization of health care - general practitioner [Month 0, 6]

    Self-reported consultation of general practitioners past 6 months (number)

  3. Change in utilization of health care - medical specialist [Month 0, 6]

    Self-reported consultation of medical specialists past 6 months (number)

  4. Change in utilization of health care - physiotherapist [Month 0, 6]

    Self-reported consultation of physiotherapists past 6 months (yes/no)

  5. Change in utilization of health care - psychologist/ psychotherapist/ psychiatrist [Month 0, 6]

    Self-reported consultation of psychologist/ psychotherapist/ psychiatrist past 6 months (yes/no)

  6. Change in utilization of health care - inpatient [Month 0, 6]

    Self-reported inpatient hospital care past 6 months (number of nights)

  7. Change in utilization of health care - outpatient [Month 0, 6]

    Self-reported outpatient hospital care past 6 months (number of admissions)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • General hospital patients admitted to participating wards of four medical departments (internal medicine, surgical medicine, trauma medicine, ear-nose-throat) at the University Medicine Hospital Greifswald in northeastern Germany
Exclusion Criteria:
  • Cognitively or physically incapable

  • Presence of a highly infectious disease

  • Discharge or transferral within the first 24 hours

  • Already asked for participation during previous hospital stay

  • Insufficient language skills

  • Employed at the conducting research institute

  • Neither telephone nor email

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Medicine Greifswald Greifswald Mecklenburg-Vorpommern Germany 17475

Sponsors and Collaborators

  • University Medicine Greifswald
  • Deutsche Krebshilfe e.V., Bonn (Germany)
  • Robert Koch Institut
  • University Hospital Schleswig-Holstein

Investigators

  • Principal Investigator: Jennis Freyer-Adam, Prof. Dr., University Medicine Greifswald, Institute of Medical Psychology
  • Principal Investigator: Ulrich John, Prof. Dr., University Medicine Greifswald, Institute CM, Department of Prevention Research and Social Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Medicine Greifswald
ClinicalTrials.gov Identifier:
NCT05365269
Other Study ID Numbers:
  • D8 5000 0001
First Posted:
May 9, 2022
Last Update Posted:
Aug 10, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 10, 2022