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Opioid-use DisorderTRECNCT03065049

Transforming Recovery Through Exercise and Community

A study testing Peer-Facilitated Counseling and Fitbit activity tracker in people with Opioid-use Disorder, run by Butler Hospital at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary aim of this study is to develop a feasible, acceptable, and effective multilevel physical activity (PA) intervention that addresses both individual and interpersonal factors that can be easily scalable and delivered in the context of a methadone clinic. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Opioid-use Disorder
What is being tested?
Peer-Facilitated Counseling and Fitbit activity tracker
Could I receive a placebo?
No, everyone receives an active treatment
How many people
81 participants
Where
1 siteUnited States
Study dates
30 Sep 2016to 31 Aug 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • receiving MMT at SSTAR and planning to remain in treatment for the next 6 months
  • low active (i.e., less than 90 minutes of MIPA per week for the past 6 months)
  • has access to a computer connected to the internet or a smartphone compatible with the Fitbit application

Who cannot join

  • a history of psychotic disorder or current psychotic symptoms
  • current suicidality or homicidality
  • marked organic impairment according to responses to the diagnostic assessments
  • physical or medical problems that would not allow safe participation in a program of moderate intensity physical activity (i.e., not medically cleared by methadone clinic physician)
  • current pregnancy or intent to become pregnant during the next 12 weeks

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Stanley Street Treatment and Resources (SSTAR) Lifeline

    Fall River, Massachusetts, 02724

Other trials in United States

About this study

Official title: Peer-Facilitated Physical Activity Intervention Delivered During Methadone Maintenance

The primary aim of this study is to develop a feasible, acceptable, and effective multilevel physical activity (PA) intervention that addresses both individual and interpersonal factors that can be easily scalable and delivered in the context of a methadone clinic. To do so, the investigators will train methadone maintenance treatment (MMT) patients who are already engaging in PA at public health recommended levels to deliver a group-based PA intervention to physically inactive MMT patients at a large community-based methadone clinic. Through the development of interpersonal relationships and social support, the investigators expect that MMT peers who have successfully navigated challenges associated with PA in this population (i.e. depression, smoking, triggers for drug use in environment) will help physically inactive MMT patients increase self-efficacy and motivation for initiating and sustaining PA.

Read the detailed description

Opioid Use Disorders (OUDs) are a highly prevalent and costly public health concern in the United States, with over 2.59 million Americans qualifying for abuse or dependence of opioids in 2015. Methadone maintenance treatment (MMT), involving daily distribution of methadone at regulated clinics, is the most common treatment for opioid use disorder. While MMT has been effective in helping OUD patients improve their quality of life, the overwhelming majority of these patients continue to engage in unhealthy lifestyles (e.g., physical inactivity and cigarette smoking) that lead to significant physical and mental health morbidities. For example, patients in MMT have much higher rates of cardiovascular disease, diabetes, hypertension, obesity, depression, sleep difficulties, and cognitive impairments than age-matched controls, which lead to premature death. Given the mental health, physical health, and drug use related benefits of physical activity (PA), interventions targeting increases in PA in patients receiving MMT could have a significant impact on reducing their overall morbidity and mortality.

To date, few PA studies have been conducted with substance abusing populations - and, only one small pilot study with MMT patients. The goal of this project is to develop a feasible, acceptable and effective multilevel PA intervention that addresses both individual and interpersonal factors that can be easily scalable and delivered in the context of a health care setting (i.e., methadone clinics). To do so, the investigators are proposing to train MMT patients who are already engaging in PA at public health recommended levels to deliver a group-based PA intervention to physically inactive MMT patients at SSTAR Lifeline, a large community-based methadone clinic in Fall River, Massachusetts. Peer-facilitated interventions for self-management skills are common in the care of patients with chronic medical conditions. Peers may play a particularly important role in increasing physical activity in MMT, as this population faces unique and significant barriers to PA (e.g., depression, smoking, minimal social supports). Through the development of interpersonal relationships, the investigators expect that MMT peers who have successfully navigated these challenges will help physically inactive MMT patients increase self-efficacy and motivation for initiating and sustaining PA.

The aims of the study include:

  1. PHASE 1 (Peer-PA Manual Development):
  • To develop a theoretically-informed peer-facilitated PA plus Fitbit (Peer-PA+Fitbit) intervention specific to SSTAR Lifeline, in order to help patients in MMT increase levels of physical activity.
  1. Focus groups will be conducted with: 1) MMT patients who are currently physically active and 2) MMT patients who are NOT meeting recommended PA levels to help inform intervention development.
  2. The investigators will: (1) develop a manualized Peer-PA intervention (that includes the use of a Fitbit activity monitor for self-monitoring PA and additional social networking), (2) create a training protocol for MMT patients to become peer-facilitators, and (3) identify safe, walkable paths in participant neighborhoods.
  3. PHASE 2 (Open Pilot):
  • An open pilot trial will be conducted with 20 MMT patients to determine the feasibility, acceptability, and short term increases in PA of the Peer-PA+Fitbit intervention. At the end of 3 months:
  1. Feedback will be obtained on Peer-PA+Fitbit from both the MMT peers and participants through self-report measures and qualitative interviews.
  2. Adherence to the intervention will be determined through group attendance and Fitbit data.
  3. Short-term increases in physical activity levels will be examined through objectively measured PA.
  4. PHASE 3 (Randomized Clinical Trial; RCT)

To conduct a 3-arm preliminary RCT of Peer-PA+Fitbit compared to Fitbit Only and compared to Usual Care (UC) among 150 MMT patients. We hypothesize that, Peer-PA+Fitbit will be superior to Fitbit Only and that Fitbit Only will be superior to UC on the following:

  1. Higher levels of short-term (3-month) and long-term (6- and 12-month) objectively-measured steps/day and moderate-to-vigorous physical activity (MVPA)
  2. Fewer days of drug use and lower levels of depression and anxiety symptoms at each follow-up
  3. Higher levels of theoretically-relevant, PA-related variables including: self-efficacy, internal motivation, and social support at 3- and 6-month follow-ups
Being tested
Peer-Facilitated Counseling, Fitbit activity tracker
Keywords
Physical Activity, Peer-facilitation, Methadone Maintenance Therapy
Medical subject headings
Opioid-Related Disorders, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Peer-Facilitated CounselingBehavioural

    Participants will engage in a 12-week physical activity intervention guided by a peer-facilitator at the methadone clinic they receive treatment. Participants will attend weekly groups, engage in a guided walking group, and utilize the Fitbit to self-monitor physical activity.

  • Fitbit activity trackerBehavioural

    Participants will be given a Fitbit activity tracker to monitor physical activity.

Study groups in NCT03065049
Study groupRoleWhat they receive
Peer-PA+FitbitExperimentalParticipants will engage in a 12-week physical activity intervention guided by a peer-facilitator at the methadone clinic they receive treatment. Participants will attend weekly groups, engage in a guided walking group, and utilize the Fitbit to self-monitor physical activity.
Receives: Behavioral: Peer-Facilitated Counseling; Behavioral: Fitbit activity tracker
Fitbit OnlyActive comparatorParticipants will be given a Fitbit activity tracker along with brief advice for increasing physical activity.
Receives: Behavioral: Fitbit activity tracker
Usual CareNo interventionParticipants do not receive any intervention but participate in the assessments only.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Minutes of moderate-to-vigorous physical activity (MVPA)/week

    Measured by accelerometry

    Measured: 12 month

Secondary outcomes (3)
  1. Acceptability of the Intervention assessed with the Client Satisfaction Questionnaire

    Client Satisfaction Questionnaire (CSQ-8)

    • Total score = summation of scores from each question
    • Maximum score for each question is 4 points (range from 1 - 4)
    • Maximum score for the measure is 32
    • The higher the total score, the better the acceptability

    Measured: 12 weeks

  2. level of depressive symptoms

    Center for Epidemiological Studies Depression Scale (CES-D)

    • Total score = summation of scores from each question
    • Scoring: 0 = Rarely or None of the time (Less than 1 day), 1 = Some or a Little of the time (1-2 days), 2 = Occasionally or a Moderate Amount of time (3-4 days), 3 = Most or All of the time (5-7 days)
    • Maximum score for the measure is 60
    • Higher scores = higher symptoms of depressive symptomatology

    Measured: 12 month

  3. level of anxiety symptoms

    Generalized Anxiety Disorder 7-item scale (GAD-7)

    • Total score = summation of scores from each question
    • Scoring for items #1-7: 0 = Not at all, 1 = Several days, 2 = Over half the days, 3 = Nearly every day
    • Item #8 is qualitative (not scored) and has the following answer choices: Not difficult at all, Somewhat difficult, Very difficult, Extremely difficult
    • Maximum score for the measure is 21
    • Higher scores = higher anxiety severity

    Measured: 12 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Feb 2017
  2. Study start30 Sep 2016
  3. Primary completion30 Aug 2022
  4. Study completion31 Aug 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
81 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03065049
Sponsor's protocol ID
1609-001
Other IDs
1R21DA041553-01A1
Acronym
TREC
Status last verified
Oct 2022
First submitted
16 Feb 2017
Last updated
4 Oct 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Peer-Facilitated Counseling and Fitbit activity tracker in people with Opioid-use Disorder, run by Butler Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Minutes of moderate-to-vigorous physical activity (MVPA)/week (time frame: 12 month). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Oct 2022.

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