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Effect of Fruit Smoothie Supplementation on Psychological Distress Among People Receiving Opioid Agonist Therapy (FruktBAR)

Primary Purpose

Substance-Related Disorders

Status
Active
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Fruit smoothie
Sponsored by
Haukeland University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Substance-Related Disorders focused on measuring Fruit, Food Supplementations, Opiate Substitution Treatment, Substance-Related Disorders

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Receiving OAT from an included outpatient clinic with outpatient follow-up on weekly basis
  • Having fruit and vegetable intake below 3 portions per day (assessed at screening)
  • Confirming interest in participating in diet intervention (criteria specified)
  • Giving informed consent

Exclusion Criteria:

  • Allergies or prior anaphylactic reactions involving fruits or vegetables
  • Poorly regulated diabetes type 1 or 2 (HbA1c >60 mmol/mol)

Sites / Locations

  • LAR Helse Stavanger HF
  • Department of Addiction Medicine, Haukeland University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Fruit smoothie

Standard

Arm Description

Participants randomised to the intervention arm will receive a 250 ml fruit smoothie as diet supplement for 20 weeks in addition to the regular OAT clinic follow-up. The fruit smoothies will be marketed products including combinations of the following fruits: apple, pineapple, mango, bananas, orange, blueberries, passion fruit, coconut, lime, and blackcurrant. The participants will receive a mixture of different smoothie types with the option of removing alternatives based on preferences. Fruit smoothie products will come in plastic bottles and will be delivered directly to the participants on a weekly basis. Each participant will receive a total of seven smoothie bottles per week with an oral agreement with each participant to consume one of these per day. Delivery of fruit smoothie will generally be given in parallel with delivery of OAT medication.

Participants randomised to standard treatment will receive regular OAT clinic follow-up without added supplementation.

Outcomes

Primary Outcome Measures

Psychological distress
The primary outcome is psychological distress assessed with the Norwegian validated translation ten item version of Hopkins Symptom Checklist (SCL-10) in the mid of the intervention period 16 weeks after initiation (12-20). This will be evaluated with mean SCL-10 item score and compared between intervention and control arm.

Secondary Outcome Measures

Biochemical indicator of inflammation
Biochemical indicators of inflammation measured with C-reactive protein in serum
Biochemical indicators of fruit intake
Biochemical indicators of fruit intake measured with serum carotenoids
Fatigue Symptom Scale
Changes in fatigue will be assessed with the Fatigue Symptom Scale (FSS-3, scale 0-18, higher values is worse)
Physical functioning
Physical functioning assessed with 4-minute step-test measuring number of steps climbed in period
Health-related quality of life
Changes in health-related quality of life will be assessed with EuroQoL EQ-5D-5L (0-100, higher is better)

Full Information

First Posted
January 24, 2022
Last Updated
October 16, 2023
Sponsor
Haukeland University Hospital
Collaborators
Helse Stavanger HF, Helse Vest, University of Bergen, ProLAR Nett, University of Oslo
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1. Study Identification

Unique Protocol Identification Number
NCT05229770
Brief Title
Effect of Fruit Smoothie Supplementation on Psychological Distress Among People Receiving Opioid Agonist Therapy
Acronym
FruktBAR
Official Title
Effect of Fruit Smoothie Supplementation on Psychological Distress Among People With Substance Use Disorders Receiving Opioid Agonist Therapy: a Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 7, 2022 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Haukeland University Hospital
Collaborators
Helse Stavanger HF, Helse Vest, University of Bergen, ProLAR Nett, University of Oslo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: People with substance use disorders generally have poor diets including limited intake of fruit and vegetables. Evidence shows substantial health benefits from increasing fruit and vegetable consumption on a variety of indicators and possibly also psychological distress. A pilot study has indicated that supplementation with fruit smoothie could be promising also among people receiving opioid agonist therapy (OAT) for opioid dependence. FruktBAR will compare the efficacy of fruit smoothie supplementation within the OAT clinics compared to standard treatment. Study design: FruktBAR is a multicentre, randomised controlled trial. The trial will recruit approximately 230 patients receiving OAT in Bergen and Stavanger, Norway. Intervention: The intervention involves daily supplementation with 250 ml fruit smoothie. The main endpoints are 16 weeks after intervention initiation. Participants will be included and followed up during and after intervention. Study population: The target group will be patients with opioid dependence receiving OAT from involved outpatient clinics in Bergen and Stavanger. Expected outcome: This study will inform on the relative advantages or disadvantages of a fruit supplementation in addition to the current medically and psychologically oriented treatment of people receiving opioid agonist therapy. If the supplementation is found to be safe and efficacious, it can be considered for further scale-up.
Detailed Description
See below each section

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance-Related Disorders
Keywords
Fruit, Food Supplementations, Opiate Substitution Treatment, Substance-Related Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants randomised to the intervention arm will receive a 250 ml fruit smoothie as diet supplement for 20 weeks in addition to the regular OAT clinic follow-up. The fruit smoothies will be marketed products including combinations of the following fruits: apple, pineapple, mango, bananas, orange, blueberries, passion fruit, coconut, lime, and blackcurrant. The participants will receive a mixture of different smoothie types with the option of removing alternatives based on preferences. Fruit smoothie products will come in plastic bottles and will be delivered directly to the participants on a weekly basis. Each participant will receive a total of seven smoothie bottles per week with an oral agreement with each participant to consume one of these per day. Delivery of fruit smoothie will generally be given in parallel with delivery of OAT medication.
Masking
Outcomes Assessor
Masking Description
Even though complete blinding is regarded as difficult and infeasible, patients will be informed of the follow-up they will receive but not on other follow-up alternatives that are used or the exact hypotheses for the study. Outcomes assessor will be blinded.
Allocation
Randomized
Enrollment
324 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fruit smoothie
Arm Type
Experimental
Arm Description
Participants randomised to the intervention arm will receive a 250 ml fruit smoothie as diet supplement for 20 weeks in addition to the regular OAT clinic follow-up. The fruit smoothies will be marketed products including combinations of the following fruits: apple, pineapple, mango, bananas, orange, blueberries, passion fruit, coconut, lime, and blackcurrant. The participants will receive a mixture of different smoothie types with the option of removing alternatives based on preferences. Fruit smoothie products will come in plastic bottles and will be delivered directly to the participants on a weekly basis. Each participant will receive a total of seven smoothie bottles per week with an oral agreement with each participant to consume one of these per day. Delivery of fruit smoothie will generally be given in parallel with delivery of OAT medication.
Arm Title
Standard
Arm Type
No Intervention
Arm Description
Participants randomised to standard treatment will receive regular OAT clinic follow-up without added supplementation.
Intervention Type
Dietary Supplement
Intervention Name(s)
Fruit smoothie
Intervention Description
Participants randomised to the intervention arm will receive a 250 ml fruit smoothie as diet supplement for 20 weeks in addition to the regular OAT clinic follow-up. The fruit smoothies will be marketed products including combinations of the following fruits: apple, pineapple, mango, bananas, orange, blueberries, passion fruit, coconut, lime, and blackcurrant. The participants will receive a mixture of different smoothie types with the option of removing alternatives based on preferences. Fruit smoothie products will come in plastic bottles and will be delivered directly to the participants on a weekly basis. Each participant will receive a total of seven smoothie bottles per week with an oral agreement with each participant to consume one of these per day. Delivery of fruit smoothie will generally be given in parallel with delivery of OAT medication.
Primary Outcome Measure Information:
Title
Psychological distress
Description
The primary outcome is psychological distress assessed with the Norwegian validated translation ten item version of Hopkins Symptom Checklist (SCL-10) in the mid of the intervention period 16 weeks after initiation (12-20). This will be evaluated with mean SCL-10 item score and compared between intervention and control arm.
Time Frame
Mid of the intervention period 16 weeks after initiation
Secondary Outcome Measure Information:
Title
Biochemical indicator of inflammation
Description
Biochemical indicators of inflammation measured with C-reactive protein in serum
Time Frame
Mid of the intervention period 16 weeks after initiation
Title
Biochemical indicators of fruit intake
Description
Biochemical indicators of fruit intake measured with serum carotenoids
Time Frame
Mid of the intervention period 16 weeks after initiation
Title
Fatigue Symptom Scale
Description
Changes in fatigue will be assessed with the Fatigue Symptom Scale (FSS-3, scale 0-18, higher values is worse)
Time Frame
Mid of the intervention period 16 weeks after initiation
Title
Physical functioning
Description
Physical functioning assessed with 4-minute step-test measuring number of steps climbed in period
Time Frame
Mid of the intervention period 16 weeks after initiation
Title
Health-related quality of life
Description
Changes in health-related quality of life will be assessed with EuroQoL EQ-5D-5L (0-100, higher is better)
Time Frame
Mid of the intervention period 16 weeks after initiation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Receiving OAT from an included outpatient clinic with outpatient follow-up on weekly basis Having fruit and vegetable intake below 3 portions per day (assessed at screening) Confirming interest in participating in diet intervention (criteria specified) Giving informed consent Exclusion Criteria: Allergies or prior anaphylactic reactions involving fruits or vegetables Poorly regulated diabetes type 1 or 2 (HbA1c >60 mmol/mol)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Fadnes, PhD
Organizational Affiliation
Haukeland University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
LAR Helse Stavanger HF
City
Stavanger
State/Province
Rogaland
ZIP/Postal Code
4010
Country
Norway
Facility Name
Department of Addiction Medicine, Haukeland University Hospital
City
Bergen
State/Province
Vestland
ZIP/Postal Code
5020
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36057629
Citation
Fadnes LT, Furulund E, Druckrey-Fiskaaen KT, Madebo T, Vold JH, Olsvold M, Pierron MC, Carlsen SL, Blomhoff R, Lid TG; ATLAS4LAR Study Group. Effect of fruit smoothie supplementation on psychological distress among people with substance use disorders receiving opioid agonist therapy: protocol for a randomised controlled trial (FruktBAR). BMC Nutr. 2022 Sep 3;8(1):97. doi: 10.1186/s40795-022-00582-z.
Results Reference
derived
Links:
URL
https://helse-bergen.no/avdelinger/rusmedisin/rusmedisin-seksjon-forsking/bar/atlas4lar-kartlegging-og-behandling-av-lungesykdom-i-legemiddelassistert-behandling
Description
Description of ATLAS4LAR

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Effect of Fruit Smoothie Supplementation on Psychological Distress Among People Receiving Opioid Agonist Therapy

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