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ObesityLEANNCT00656045

Leisure Time Activity and Nutrition Program

A study testing Dietary, Physical Activity and TV Watching in people with Obesity and Physical Activity, run by The University of Tennessee, Knoxville 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 purpose of this investigation is to conduct an 8-week pilot study to examine the effects of two different leisure-time activity prescriptions on dietary intake, leisure-time activities, and weight loss in 26 adults receiving a standard 8-week behavioral weight loss intervention. Read more about this study

Who is it for?
Ages 21 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Obesity, Physical Activity
What is being tested?
Dietary, Physical Activity and TV Watching
Could I receive a placebo?
No, everyone receives an active treatment
How many people
24 participants
Where
1 siteUnited States
Study dates
Mar 2008to Sep 2008
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 21 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Body mass index (BMI) between 25 and 40 kg/m2
  • Watch > 16 hours per week of TV
  • Engage in < 100 minutes of moderate-intense physical activity per week

Who cannot join

  • Participants reporting a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Individuals self-reporting joint problems, prescription medication usage related to heart conditions, or other medical conditions that could limit exercise will be required to obtain written physician consent to participate.
  • Reporting they are unable to walk for 2 blocks (1/4 mile) without stopping.
  • Reporting no TVs in the home or 5 or more TVs in the home viewed by the participant (TVs in participant's children's bedrooms will not be counted).
  • Reporting major psychiatric diseases or organic brain syndromes via a phone screen.
  • Participating in a weight loss program and/or taking weight loss medication or that have lost > 5% of body weight during the past 6 months.
  • Participating in a program to increase physical activity and/or decrease TV watching time.
Show all 10Show fewer
  • Intending to move to another city within the time frame of the investigation.
  • Being pregnant, lactating, less than 6 months post-partum, or planning to become pregnant during the time frame of the investigation.
  • Having had gastric surgery for weight loss.
  • Being unwilling to attend weekly sessions.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Tennessee

    Knoxville, Tennessee, 37996

Other trials in United States

About this study

Official title: The Effects of Two Different Leisure-time Activity Prescriptions on Eating and Activity Behaviors During Behavioral Weight Loss Treatment

The purpose of this investigation is to conduct an 8-week pilot study to examine the effects of two different leisure-time activity prescriptions on dietary intake, leisure-time activities, and weight loss in 26 adults receiving a standard 8-week behavioral weight loss intervention.

Read the detailed description

In adult observational studies, TV viewing has been positively related to overweight and obesity. It is theorized that TV watching influences eating and activity behaviors, such that with greater TV watching less physical activity and greater consumption of energy occurs, producing a positive energy balance state. While no experimental research has been conducted with adults examining the influence of reducing TV watching on weight status, experimental research conducted with children does indicate that lower levels of TV watching can produce reduced energy intake and greater levels of physical activity. Most importantly, family-based, behavioral childhood obesity interventions that have targeted reducing sedentary behaviors (which includes TV watching) have found that as compared to targeting increasing physical activity during treatment, similar increases in activity and fitness occur, but that greater weight loss and greater increases in liking for physical activity occur when sedentary behaviors, as compared to physical activity, are targeted in family-based behavioral childhood weight control programs.

Thus, this investigation will involve an 8-week pilot study to examine the effects of two different leisure-time activity prescriptions. All participants in the investigation will receive a standard 8-week behavioral obesity intervention. The intervention will include a reduced caloric prescription (1200-1500 kcal/day) and fat gram prescription (30% or less kcals from fat). One condition will receive an activity goal (200 minutes/week of moderate-intense physical activity [Physical Activity]), while the other condition will receive a TV watching goal (10 hours/week [ TV Watching]). Participants will be assessed at 0 and 9 weeks (pre- and post-intervention) on measures of dietary intake, physical activity, TV watching, liking of physical activity and TV watching, and weight.

Being tested
Dietary, Physical Activity, TV Watching
Keywords
Obesity, Physical Activity, Weight Loss, Exercise, Dietary Intake, Energy, Behavioral, Healthy Eating
Medical subject headings
Obesity, Motor Activity, Weight Loss, Behavior

What participants receive

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

  • DietaryBehavioural

    All participants in the investigation will receive a standard 8-week behavioral obesity intervention with 8 weekly, 1 hour group counseling and education sessions. The intervention will include a reduced caloric prescription (1200-1500 kcal/day) and fat gram prescription (30% or less kcals from fat).

  • Physical ActivityBehavioural

    The Physical Activity arm will receive an activity goal (200 minutes/week of moderate-intense physical activity).

  • TV WatchingBehavioural

    The TV Watching arm will receive a TV watching goal of watching less than 10 hours of TV/week.

Study groups in NCT00656045
Study groupRoleWhat they receive
AExperimentalArm A focuses on increasing the participant's physical activity level.
Receives: Behavioral: Dietary; Behavioral: Physical Activity
BExperimentalArm B focuses on decreasing the amount of time the participant spends watching Television.
Receives: Behavioral: Dietary; Behavioral: TV Watching

What is being measured

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

  1. Time spent in moderate-intense physical activity

    Measured: 8 weeks

Secondary outcomes (4)
  1. Weight loss

    Measured: 8 weeks

  2. Caloric and fat intake while watching TV

    Measured: 8 weeks

  3. Liking of physical activity

    Measured: 8 weeks

  4. Time spent watching TV

    Measured: 8 weeks

Timeline

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

  1. First posted10 Apr 2008 (estimated)
  2. Study startMar 2008
  3. Primary completionJul 2008
  4. Study completionSep 2008

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
Single blind
Who is masked
Outcomes assessor
Enrolment
24 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00656045
Sponsor's protocol ID
LEAN E01-1703-011
Acronym
LEAN
Status last verified
Apr 2018
First submitted
4 Apr 2008
Last updated
5 Apr 2018
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Dietary, Physical Activity and TV Watching in people with Obesity and Physical Activity, run by The University of Tennessee, Knoxville 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 10 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 5 Apr 2018. 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?

Time spent in moderate-intense physical activity (time frame: 8 weeks). 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 5 Apr 2018.

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Leisure Time Activity and Nutrition Program | AzTrials