| Literature DB >> 25833668 |
Leila Amiri Farahani1, Mohsen Asadi-Lari2, Eesa Mohammadi3, Soroor Parvizy4, Ali Akbar Haghdoost5, Ziba Taghizadeh6.
Abstract
OBJECTIVE: Review and assess the effectiveness of community-based physical activity interventions among women aged 18-65 years.Entities:
Mesh:
Year: 2015 PMID: 25833668 PMCID: PMC4390687 DOI: 10.1136/bmjopen-2014-007210
Source DB: PubMed Journal: BMJ Open ISSN: 2044-6055 Impact factor: 2.692
A sample of the search string was used in the study
| Databases (hits) | Key words used |
|---|---|
| PubMed (n=467) | (1) physical activity; (2) physical inactivity; (3) exertion; (4) fitness; (5) community-based intervention; (6) community-based research; (7) population-based intervention; (8) community-based research; (9) 1 or 2 or 3 or 4 or 5 or 6 or 7 or 8; (10) randomised controlled trial; (11) controlled trial; (12) 9 and 10; (13) 9 and 11 |
The inclusion and exclusion criteria for selecting the studies on the basis of PICOS
| PICOS criteria | |
|---|---|
| Participants |
Participants were to be 18–65 years of age. The study did not involve disease-state populations (for example multiple sclerosis rehabilitation patients. |
| Interventions |
Interventions must be designed to improve PA and to prevent physical inactivity, cardiovascular disease, diabetes and other side effects of sedentary life style. The study only included community-based interventions. |
| Comparisons |
Studies must provide an assessment of an intervention group through comparison with a control or comparison group which was simultaneously derived from the same or similar settings. |
| Outcomes |
Participants were to be 18–65 years of age. Participation in PA must be one of the measured outcomes. Studies must at least demonstrate a specific measure of PA (objective, self-reported or both) at the baseline and follow-up. |
| Study design |
In this review articles with both random and non-random allocation of participants to study groups were included, but results from observational studies were not reported. |
Methodological quality scores and ratings
| Study | Item scoring | |||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Patient Selection | Blinding | Interventions | Outcomes | Statistics | Scores/ Rating | |||||||||||||||||||||||||||||||||||
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36 | 37 | 38 | 39 | ||
| Albright | 1 | 1 | 0 | 0 | 0 | 1 | NA | NA | 0 | NA | NA | 0 | 1 | 0 | NA | NA | NA | 1 | 0 | 1 | 0 | 1 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | 0 | 1 | NA | 0.56/high |
| Gaston | 1 | 0 | 0 | 0 | 0 | 1 | NA | NA | 1 | NA | NA | 0 | 1 | 0 | NA | NA | NA | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | NA | 0.44/low |
| Keyserling | 1 | 1 | 1 | 1 | 1 | 1 | NA | NA | 1 | NA | NA | 0 | 1 | 0 | NA | NA | NA | 0 | 0 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | NA | 0.78/high |
| Lombard | 1 | 1 | 1 | 1 | 1 | NA | NA | 1 | NA | NA | 1 | 1 | 0 | NA | NA | NA | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | NA | 0.62/high | |
| Napolitano | 1 | 1 | 0 | 0 | 0 | 1 | NA | NA | 1 | NA | NA | 0 | 1 | 1 | NA | NA | NA | 0 | 0 | 1 | 1 | 0 | 0 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | 0 | 1 | NA | 0.59/high |
| Pazoki | 1 | 1 | 0 | 0 | 0 | 1 | NA | NA | 0 | NA | NA | 0 | 0 | 1 | NA | NA | NA | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 1 | 1 | NA | 0.4/low |
| Ransdell | 1 | 1 | 0 | 0 | 0 | 0 | NA | NA | 0 | NA | NA | 0 | 1 | 0 | NA | NA | NA | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | NA | 0.5/low |
| Sharpe | 1 | 0 | 0 | 0 | 0 | 1 | NA | NA | 0 | NA | NA | 0 | 1 | 1 | NA | NA | NA | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | 1 | 1 | 1 | 0 | 0 | 1 | NA | 0.47/low |
| Yancey | 1 | 1 | 1 | 1 | 1 | 1 | NA | NA | 1 | NA | NA | 0 | 1 | 1 | NA | NA | NA | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | NA | 0.72/high |
1, eligibility criteria; 2, described as randomised; 3, randomisation performed; 4, randomisation described as appropriate; 5, randomisation concealed; 6, baseline comparability; 7, described as double blind; 8, blinding described as appropriate; 9, blinding of investigator/assessor;10, blinding of subject/patient; 11, blinding of therapist; 12, blinding of the outcome (results); 13, treatment protocol adequately described for the treatment and control groups; 14, control and placebo adequate; 15, cointerventions avoided or comparable; 16, cointerventions reported for each group separately; 17, control for cointerventions in design; 18, testing of subject adherence; 19, adherence acceptable in all groups; 20, description of withdrawals and dropouts; 21, withdrawals/dropouts rate described and acceptable; 22, reasons for dropouts; 23, adverse effects described; 24, follow-up details reported; 25, follow-up period adequate; 26, short follow-up performed; 27, timing of outcomes comparable in all groups; 28, description of outcome measures; 29, relevant outcomes included; 30, validity reported for main outcome measure; 31, reliability reported for main outcome measure; 32, responsiveness reported for main outcome measure; 33, use of quantitative outcome measures; 34, descriptive measures reported for the main outcome; 35, appropriate statistical analysis included; 36, sample size calculated a priori; 37, adequate sample size; 38, sample size described for each group; 3, intention-to-treat analysis included; NA, not applicable.
Figure 1Flow diagram used for the identification, screening, eligibility and inclusion of studies.23
Characteristics of included studies
| Study (year)ref | Country | Design of study | Population (n) | General intervention | Outcome measure | Measurement times | Results |
|---|---|---|---|---|---|---|---|
| Albright | USA | CT | Baseline: Phone+Mail Counselling group=35, Mail Support group=37; there are no exact information for follow-ups |
All participants received 2 months of Weekly 1 h classes (group activities, small-group discussions, and question-and-answer games). Random allocation to 10 months of either home-based telephone counselling, additional information, and feedback for PA by mailed newsletters (Phone+Mail Counselling condition) or only the mailed newsletters (Mail Support condition). | PA | Baseline, 10 weeks, 6 and 12 months after baseline |
There was not any significant difference in the percentage of participations in 30 or more of MVPA at least 5 days weekly between the Phone+Mail Counselling group (49%) and Mail Support group (35%) after 12 months Results of between group comparison after 10 months showed, there is a significantly greater increase in total energy expenditure via PA in phone+mail counselling group than the mail support group (p<0.05) |
| Gaston | USA | CT | Baseline: intervention group=106, comparison group=28; follow-up (10 weeks): intervention group=83, comparison group=23; follow-up (6 months): intervention group=?, comparison group=?, sample size in both groups: 42; follow-up (12 months): intervention group=45, comparison group=7 |
Intervention group received curriculum-, culture- and gender-specific based approaches to behavioural change. Participants were divided into 10 structured intervention groups with 8–13 women per group. The groups met for 90 min for 10 weeks, led by facilitators and received the Gaston book. All participants signed a group contract for improving PA at the first session. Control group received the copy of the Gaston but did not receive a curriculum, facilitator and expert consultants. | Perception of overall health, Health attitudes, eating patterns and PA | Baseline,10 weeks, 6 and 12 months |
Statistically significant increase in the women’s involvement in aerobic exercise (from 1.9 day per wk at baseline to 3.97, 2.48 and 3.21 day per week at 10 weeks, 6 and 12 months). A significant.10-week difference was found in the women’s diet, with them reporting eating more nutritious foods (p<0.001) |
| Keyserling | USA | RCT | Baseline: EI group=118, MI group=118; follow-up (6 months): EI group=108, MI group=110; follow-up (12 months): EI group=106, MI group intervention=106 |
EI group received two 6-month phases, first phase included 3 group sessions, 2 individual counselling sessions, and 3 phone calls from an expert counsellor; second phase (maintenance phase) included 1 individual counselling session and 7 monthly peer counsellor calls. MI group consisted of a one-time mailing of pamphlets on PA and diet | PA, Dietary intake, fasting blood lipids, blood pressure, weight, and psychosocial variables | Baseline, 6 and 12 months |
PA outcomes by using a questionnaire: at the 6 and 12 month follow-up, the EI group reported significantly more moderate (p=0.001) and vigorous (p=0.03) PA and there is no significant differences between EI and MI groups by using accelerometer at 6 and 12 months(p>0.05). Dietary intake improved more in the EI compared to the MI (questionnaire at 6 and 12 months, p=0.001; serum carotenoid index, p=0.05) |
| Lombard | Australia | RCT | Baseline: intervention group=127, comparison group=123; follow-up (4 months): intervention group=88, comparison group=85 |
Intervention group consisted of 4 sessions including 3 1 h interactive group sessions in the first month plus one review session at 4 months; Content included messages with clear goals on PA and behaviour change. Participants were encouraged to enter voluntary school-based walking groups or to walk with friends for social support; moreover, they used pedometer for self-monitoring, and received one instruction for using it. Comparison group participated in individual 30 mins, non-interactive health education group lecture and received a pedometer without setting the goal. | PA, diet, self-monitoring, self-efficacy, anthropometric measures | Baseline and 4 months |
The intervention group reported more improvements in PA level even though the difference between the two groups was not significant. The difference in scores between groups on the basis of MET was 35 (−315 to 416), 67 (−389 to 525), 46 (−412 to 506) for walking, moderate and vigorous PA, respectively Participants in both groups decreased weight with no significant difference between groups (p=0.95) |
| Napolitano | USA | CT | Baseline: CTM=93, Jumpstart=95, Wellness control=92; number of participants did not report for follow-ups 1, 3, 6 and 12 months |
CTM group received a 12-week programme and one mailing booklet covering a topic weekly on the basis of American Heart Association guideline for PA. The Jumpstart group completed a 65-item questionnaire for assessing the stage of change, processes of change and self-efficacy related to PA at baseline and prior to the 1-month, 3-month and 6-month time points. Participants received a booklet matched to stage of change and an individually tailored feedback report addressing barriers, benefits, self-efficacy, social support and goal setting. The Wellness group received one mailing of women’s health information about sleep, cancer prevention, and nutrition. | PA, stage of change, process of change, self-efficacy | Baseline, 3 and 12 months |
At 3 months, participants in the Jumpstart group reported significantly more minutes of PA per week than participants in the Wellness group (respectively, 140.4±14.82, 98.1±15.09) (p<0.05). The Jumpstart group showed an inclination towards significance (p=0.054) when compared with the CTM group (99.5±15.11); there was no significant difference between the CTM and Wellness groups. At 12 months, no significant differences existed between any of the treatment groups |
| Pazoki | Iran | CT | Baseline: Intervention=179, control=179; follow-up (8 weeks): Intervention=170, control=160 |
The intervention group received an 8-week programme related to the American Heart Association PA for women, audio-taped activity instructions and an educational package which were given weekly thorough home-visits by local volunteers. Control group: not reported. | PA | At baseline and 8 weeks |
Increasing in PA from 3% and 2.7% at baseline to 13.4% and 3% after 8 weeks in the intervention and control groups. Intervention group reported more minutes of PA per wk(mean=139.81, SE=23.35) than women in the control group (mean=40.14, SE=12.65) at week 8 and the difference between two groups was statistically significant (p<0.0001) |
| Ransdell | USA | CT | Baseline: home-based intervention=20, community-based intervention=20; follow-up: home-based intervention=14, community-based intervention=20 |
CB activities were completed at a fitness facility within a university and met 3 times per week and fitness-oriented activities 2 times a week, Fitness activity days lasted 60–75 min and consisted of a 5 min warm-up, 20–30 min of aerobic activity, 20–30 min of weight training, and 5–10 min of stretching and abdominal strengthening exercises. HB group received a detailed packet including a calendar of recommended activities, pictures of various stretches, and strength-training activities, plus some advice for overcoming barriers, and sent or faxed their PA logs to the lead author every 2 weeks. | PA, health-related fitness, BP | At baseline and 12 weeks |
There were no differences between changes in PA for home-based and community-based groups. Mothers and daughters in both groups significantly increased their participation in aerobic, muscular strength, and flexibility activities (p=0.02 to 0.000). |
| Sharpe | USA | CT | Baseline: full intervention=430, community-media exposure only=245, no intervention: 234 ; follow-up: full intervention=217, community-media exposure only=820, no intervention: 822 |
Intervention consisted of two components: (a) a year-long media campaign to increase moderate-intensity exercise, where 27 women from the community were social models and their photos were in print and television sports and participated in the 13 monthly exercise events. (b) Behavioural intervention consisted of an intensive, 24-week, minimal-contact intervention which included an orientation packet and weekly tips, a pedometer, a guide to exercise and a goal-setting. Women participated in group exercise which gave them an opportunity to enjoy new activities and meet exercise partners. Group 1 received the full intervention, enrolled in the full 24-week behavioural programme and was exposed to countywide media messages. Group 2 lived in the media exposed county but not enrolled in the behavioural intervention. Group 3 received no intervention. | PA, self-efficacy, anthropometric in formation, counting steps | Baseline and 12 months |
Behavioural intervention with media messages was more effective than media messages alone or no intervention Women in the behavioural intervention had the greatest pre- to post-programme positive differences and had significantly higher recall of programme ads and of the main message than did the media only sample |
| Yancey | USA | RCT | Baseline: intervention=193, ccontrol=183; follow-up (2 months): intervention=158, control=156; follow-up (6 months): intervention=118, control=110; intervention (12 months)=135, control=128 |
The intervention group included 8 weekly 2 h interactive group sessions, skills training in a regular exercise regimen, interview by a dietician about their food intake 3 or 4 times during the intervention and feedback on the quality and adequacy of their intake. Participants were encouraged to invite one close female relative or friend to accompany them during postintervention use of health club facilities. Control group received 8 weekly, 2 h interactive group sessions on health topics such as tobacco and cancer screening without the external social support. | BIA, WHR,BMI, sedentary behaviour, PA, fitness | At baseline, 2, 6, and 12 months |
There was a significant effect of the intervention on PA at 2 months (p=0.0148), remaining marginally significant at 12 months (p=0.058) Participants in the intervention group showed a trend toward weight stability at 2 months compared with control group (p=0.75; p=0.08, respectively), disappearing at 12 months (p=0.0001; p=0.001, respectively) |
BIA, bioelectrical impedance analyser; CAB, Community Advisory Board; COMBO, pedometer-plus group; CTM, choose to move; EI, enhanced intervention; MET, metabolic equivalent; MI, minimum intervention; MVPA, moderate-to-vigorous physical activity; PED, pedometer-only group; TTM, trans-theoretical model; WHR, waist/hip ratio.