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N/A Completed N=64 Randomized Treatment

RELAX: A Mobile Application Suite Targeting Obesity and Stress

Stress · Weight
Source: ClinicalTrials.gov NCT02615171 ↗
Enrolled (actual)
64
Serious AEs
0.0%
Results posted
Mar 2021
Primary outcomePrimary: Percentage of Days App Used Over 12 Weeks — 57.5; 53.8 percent of days app used

Summary

This research is being done is to evaluate the feasibility and acceptability of a novel weight loss mobile app that was designed to be less burdensome than traditional weight loss apps.

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Days App Used Over 12 Weeks
57.5; 53.8
PRIMARY
Usability
76.3; 64.8 0.0106 sig
PRIMARY
Acceptability
77; 39 0.0027 sig
PRIMARY
Burden
45.0; 30.0 0.7829
SECONDARY
Percent Weight Change From Baseline to 12-Week Follow-Up
-3.6; -3.0
SECONDARY
Change in Perceived Stress From Baseline to 12-Week Follow-Up
2.8; 2.5
SECONDARY
Change in Emotional Eating From Baseline to 12-Week Follow-Up
-1.1; -9.9

Eligibility Criteria

Inclusion Criteria

  • Have a BMI of 27-45
  • Currently use an Android smartphone
  • Have cell phone connectivity at home and work
  • Uses a smartphone every day

Exclusion Criteria

  • Under the age of 18 and over the age of 65;
  • BMI under 27 or over 45;
  • Not interested in losing weight;
  • Does not currently own a smartphone;
  • Smartphone type and/or version not meeting app requirements;
  • No phone connectivity at home and work;
  • Unable to walk unaided for ¼ mile without stopping;
  • Has a condition that precludes dietary changes (i.e. ulcerative colitis, Crohn's disease, active diverticulitis, renal disease);
  • On a medication affecting weight;
  • Type 1 or 2 diabetes;
  • Had gastric bypass surgery;
  • Had or plans to have gastric bypass surgery during the study period;
  • Pregnant/lactating;
  • Has bipolar disorder, substance abuse, bulimia, or severe depression;
  • Lost 5% or more body weight in the last 3 months;
  • Has not experienced emotional eating over the last week;
  • On medication affecting weight;
  • Has concerns about being audiotaped;
  • Prisoner;
  • Unable to provide consent; or
  • Non-English speaking
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02615171). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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