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Weight Loss Intervention for Individuals With Lower Extremity Amputation (MOVE-LEAP)

Primary Purpose

Lower Extremity Amputation

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Coached group
Self-directed control group
Screened only
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lower Extremity Amputation focused on measuring weight loss, exercise, home-based, lower extremity amputation, pilot study

Eligibility Criteria

18 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Lower extremity amputation (including toes) for at least 1 year
  • overweight or obese
  • <60 minutes drive-time to VA Puget Sound Health Care System - Seattle campus, willing to be randomized
  • provides written, informed consent
  • able to perform some form of aerobic exercise (e.g., walking, bicycling, swimming)
  • has telephone
  • able to complete study assessments

Exclusion Criteria:

  • Co-morbidities which may be contraindicated or indicate no potential benefit from weight loss or increasing physical activity
  • unlikely to be able to adhere to study protocol and complete questionnaires and measurements reliably
  • recent or current (last 6 months) participation in a weight loss program, including taking weight loss medications
  • only uses motorized (non-manual) wheelchair

Sites / Locations

  • VA Puget Sound Health Care System Seattle Division, Seattle, WA

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Other

Arm Label

Coached

Self-directed

Screened

Arm Description

Participants randomized to the coached arm will receive the same educational and self-monitoring materials as the self-directed group. In addition, participants in the coached arm will receive 11 calls from a health coach and a single visit to their home by an exercise specialist.

Participants randomized to the self-directed arm will receive the same educational and self-monitoring materials as the coached group, but no home visit and no coaching calls. They will be encouraged to make behavior changes on their own.

Individuals who were contacted to inform them about the study or who contacted study personnel to express an interest in participating. This group is presented in order to present statistics on feasibility regarding recruitment

Outcomes

Primary Outcome Measures

Number of Individuals That Were Randomized of Those Contacted (Feasibility)
Specific components include yield by method, recruitment rate, refusal rates and reasons

Secondary Outcome Measures

Feasibility - Retention
Number of randomized individuals who complete baseline and study exit visit
Acceptability
Acceptability of intervention will be assessed via a brief satisfaction survey - % who would recommend the program to a friend
Change in Weight
Changes between baseline and 20-weeks later (end of intervention)
Change in 6-minute Walk Distance
Change in 6-minute walk distance (ft) from baseline to follow-up

Full Information

First Posted
January 17, 2014
Last Updated
May 2, 2018
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT02085785
Brief Title
Weight Loss Intervention for Individuals With Lower Extremity Amputation
Acronym
MOVE-LEAP
Official Title
Home-based Weight Loss Intervention for Individuals With Lower Extremity Amputation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
February 20, 2014 (Actual)
Primary Completion Date
November 16, 2015 (Actual)
Study Completion Date
May 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to pilot test a program to help overweight and obese individuals with a lower extremity amputation (LEA) lose weight and become more physically active. The investigators will randomize approximately 30 individuals to either a self-directed weight loss program (n=15) or a coached weight loss program (n=15). The primary purpose of this pilot study is to determine if a home-based weight loss/physical activity (PA) intervention is feasible in individuals with a LEA. MOVE-LEAP is a 20-week program that involves 11 phone calls from a health coach and a single home visit by a physical therapist. This pilot study aims to: test the feasibility of recruiting overweight/obese individuals with LEA into a randomized trial; assess whether the intervention can be delivered with high fidelity, and evaluate whether the intervention is acceptable to and safe as determined by participant feedback, participation and retention for outcome measures.
Detailed Description
Participants randomized to the intervention arm will receive (1) a home visit by an exercise specialist and (2) a 20-week telephone-delivered weight loss program, modeled on the VA's Telephone Lifestyle Coaching Program (MOVE!TLC). All participants (both the coached arm and self-directed arm) will be mailed a MOVE-LEAP packet [containing eating and physical activity logs, information on how to set weight loss goals, suggestions for physical activity/exercise, dietary guides, etc.), a MOVE-LEAP handout booklet, calories counting book, a pedometer, exercise digital versatile disc (DVD), and a flip-booklet with exercises ("Exercise Guide for Persons with Limb Loss"). A bathroom scale will be provided for participants who do not already own one. Participants in the coached arm will receive a home visit by an exercise specialist. This visit will occur 1-3 weeks after randomization. The exercise specialist will assess the participant's capabilities and interest regarding physical activity as well as his/her home environment for physical activity. Since each participant may have different physical capabilities and limitations, the type and intensity of physical activity will be tailored to each participant's preferences and their home and neighborhood/community environment and resources. If the participant is interested in performing physical activity outside their home, study staff will provide them with information about community resources for physical activities. Participants in the coached arm will receive 11 calls by a study health coach. During the phone calls (weekly initially and then every other week), the health coach will review progress and help the participant to set "SMART" goals (Specific, Measurable, Attainable, Relevant and Time-limited) and will use motivational interviewing techniques to help the participant achieve those goals. Motivational interviewing is a style of counseling meant to increase participant engagement through strategic use of open-ended questions, reflective listening and positive affirmations. The study staff will review the participant's progress on his or her goals and help him or her problem solve to resolve challenges and modify goals as needed. During each session, the coach will discuss an educational topic relating to weight loss. Written materials on each topic are included the booklet.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lower Extremity Amputation
Keywords
weight loss, exercise, home-based, lower extremity amputation, pilot study

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Coached
Arm Type
Experimental
Arm Description
Participants randomized to the coached arm will receive the same educational and self-monitoring materials as the self-directed group. In addition, participants in the coached arm will receive 11 calls from a health coach and a single visit to their home by an exercise specialist.
Arm Title
Self-directed
Arm Type
Active Comparator
Arm Description
Participants randomized to the self-directed arm will receive the same educational and self-monitoring materials as the coached group, but no home visit and no coaching calls. They will be encouraged to make behavior changes on their own.
Arm Title
Screened
Arm Type
Other
Arm Description
Individuals who were contacted to inform them about the study or who contacted study personnel to express an interest in participating. This group is presented in order to present statistics on feasibility regarding recruitment
Intervention Type
Behavioral
Intervention Name(s)
Coached group
Intervention Description
Participants randomized to the coached arm will receive 1) education and self-monitoring materials [e.g., a booklet, calorie count book, pedometer, and scale (if they do not have one)], 2) a home visit by an exercise specialist, and 3) 11 telephone calls (over a 20-week period) by a health coach who will utilize motivational interviewing techniques to help the participant set eating and activity goals and trouble shoot problems when they occur
Intervention Type
Behavioral
Intervention Name(s)
Self-directed control group
Intervention Description
Participants randomized to the self-directed control arm will receive the same educational and self-monitoring materials as the coached group [e.g., a booklet, calorie count book, pedometer, and scale (if they do not have one)], but no home visit and no coaching calls. They will be encouraged to make behavior changes on their own.
Intervention Type
Other
Intervention Name(s)
Screened only
Intervention Description
Screened only - No intervention -- individuals who are contacted and/or screened for eligibility
Primary Outcome Measure Information:
Title
Number of Individuals That Were Randomized of Those Contacted (Feasibility)
Description
Specific components include yield by method, recruitment rate, refusal rates and reasons
Time Frame
During recruitment (expected duration of 12-15 months)
Secondary Outcome Measure Information:
Title
Feasibility - Retention
Description
Number of randomized individuals who complete baseline and study exit visit
Time Frame
Follow-up assessments (all participants) and during intervention (intervention group only) (weekly, for 20 weeks)
Title
Acceptability
Description
Acceptability of intervention will be assessed via a brief satisfaction survey - % who would recommend the program to a friend
Time Frame
At follow-up assessment (20-weeks follow-up)
Title
Change in Weight
Description
Changes between baseline and 20-weeks later (end of intervention)
Time Frame
Baseline and follow-up assessment (20-weeks after randomization)
Title
Change in 6-minute Walk Distance
Description
Change in 6-minute walk distance (ft) from baseline to follow-up
Time Frame
Baseline and at follow-up assessment (20-weeks after randomization)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Lower extremity amputation (including toes) for at least 1 year overweight or obese <60 minutes drive-time to VA Puget Sound Health Care System - Seattle campus, willing to be randomized provides written, informed consent able to perform some form of aerobic exercise (e.g., walking, bicycling, swimming) has telephone able to complete study assessments Exclusion Criteria: Co-morbidities which may be contraindicated or indicate no potential benefit from weight loss or increasing physical activity unlikely to be able to adhere to study protocol and complete questionnaires and measurements reliably recent or current (last 6 months) participation in a weight loss program, including taking weight loss medications only uses motorized (non-manual) wheelchair
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alyson J. Littman, PhD MPH
Organizational Affiliation
VA Puget Sound Health Care System Seattle Division, Seattle, WA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Puget Sound Health Care System Seattle Division, Seattle, WA
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
30115584
Citation
Littman AJ, Haselkorn JK, Arterburn DE, Boyko EJ. Pilot randomized trial of a telephone-delivered physical activity and weight management intervention for individuals with lower extremity amputation. Disabil Health J. 2019 Jan;12(1):43-50. doi: 10.1016/j.dhjo.2018.08.002. Epub 2018 Aug 10.
Results Reference
derived

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Weight Loss Intervention for Individuals With Lower Extremity Amputation

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